{ "name": "FDA Dietary Supplement Recalls (openFDA enforcement reports)", "license": "https://creativecommons.org/licenses/by/4.0/", "attribution": "Verified Supplement Data, https://verifiedsupplementdata.com/recalls/", "source": "FDA enforcement reports via openFDA food/enforcement endpoint", "sourceUrl": "https://open.fda.gov/apis/food/enforcement/", "queries": [ "product_description:\"dietary supplement\" AND report_date:[20230101 TO 20991231]", "product_type:\"Food\" AND (product_description:supplement OR product_description:vitamin OR product_description:capsules) AND report_date:[20230101 TO 20991231]" ], "fetchedOn": "2026-09-21", "since": "2023-01-01", "methodology": "Two openFDA food/enforcement searches merged on recall_number; conventional foods matched by the broader search are dropped by a keep-filter; records sharing an FDA event_id are grouped into one event. `category` is assigned by keyword from FDA's reason_for_recall in a fixed order (tainted > contamination > allergen > labeling > other); `ingredientSlugs` are exact-name matches of the product description against the ingredient clusters this site covers, with excipients removed first. Both are ours, not FDA's.", "totals": { "records": 194, "events": 89, "byClass": { "Class I": 34, "Class II": 123, "Class III": 37 }, "byYear": { "2023": 84, "2024": 19, "2025": 60, "2026": 31 }, "byCategory": { "contamination": 87, "labeling": 55, "allergen": 27, "tainted": 19, "other": 6 }, "byStatus": { "Terminated": 156, "Ongoing": 33, "Completed": 5 }, "byIngredient": { "b12": 5, "vitamin-c": 4, "methylfolate": 4, "multivitamins": 4, "b-complex": 3, "elderberry": 3, "iron": 3, "vitamin-d": 3, "biotin": 3, "omega-3": 2, "colostrum": 2, "spirulina": 2, "protein": 2, "calcium": 2, "lutein-zeaxanthin": 1, "probiotics": 1, "bromelain": 1, "boswellia": 1, "glutathione": 1, "taurine": 1, "quercetin": 1, "pine-bark-extract": 1, "l-glutamine": 1, "lactoferrin": 1, "spermidine": 1, "flaxseed-oil": 1, "phosphatidylserine": 1, "psyllium": 1, "collagen": 1, "vitamin-b6": 1, "choline": 1, "myo-inositol": 1, "digestive-enzymes": 1, "chromium": 1 } }, "last12Months": { "from": "2025-09-21", "total": 67, "byClass": { "Class I": 18, "Class II": 34, "Class III": 15 }, "byCategory": { "labeling": 28, "allergen": 15, "contamination": 15, "tainted": 8, "other": 1 }, "events": 34 }, "categoryLabels": { "tainted": "Hidden drug or prohibited ingredient", "contamination": "Contamination (microbial, heavy metal, foreign matter)", "allergen": "Undeclared allergen", "labeling": "Labeling or potency", "other": "Other" }, "eventPages": [ "https://verifiedsupplementdata.com/recalls/2026-09-zmb-enterprises/", "https://verifiedsupplementdata.com/recalls/2026-08-factory6/", "https://verifiedsupplementdata.com/recalls/2026-07-total-nutrition/", "https://verifiedsupplementdata.com/recalls/2026-07-modern-warrior-life/", "https://verifiedsupplementdata.com/recalls/2026-07-mogo-moringa/", "https://verifiedsupplementdata.com/recalls/2026-06-total-nutrition/", "https://verifiedsupplementdata.com/recalls/2026-04-pure-vitamins-and-natural-supplements/", "https://verifiedsupplementdata.com/recalls/2026-04-siluetaya/", "https://verifiedsupplementdata.com/recalls/2026-02-superfoods/", "https://verifiedsupplementdata.com/recalls/2025-07-vita-warehouse/", "https://verifiedsupplementdata.com/recalls/2025-05-my-life/", "https://verifiedsupplementdata.com/recalls/2025-04-supplement-manufacturing-partner/" ], "events": [ { "event_id": "99629", "recalling_firm": "Byron White Formulas, Inc.", "city": "Santa Rosa", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-09-02", "recall_initiation_date": "2026-08-11", "reason_for_recall": "Label does not declare walnuts in English", "category": "allergen", "distribution_pattern": "Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1276-2026", "H-1277-2026", "H-1278-2026" ], "product_short": "Byron White FORMULAS A-L Complex", "product_count": 3, "slug": null }, { "event_id": "98691", "recalling_firm": "ZMB Enterprises", "city": "Carlsbad", "state": "CA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-09-02", "recall_initiation_date": "2026-04-03", "reason_for_recall": "The product contains 1,4-DMAA, Phenylethylamine and Phenibut.", "category": "tainted", "distribution_pattern": "The firm markets their products online via their website addallxr.com", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1263-2026" ], "product_short": "Addall XR Shot", "product_count": 1, "slug": "2026-09-zmb-enterprises", "title": "Addall XR Shot Recall (September 2026): Reason, Lots, What to Do" }, { "event_id": "99425", "recalling_firm": "FACTORY6, INC.", "city": "Lindon", "state": "UT", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-08-12", "recall_initiation_date": "2026-07-19", "reason_for_recall": "Possible Salmonella in Moringa Leaf Powder product.", "category": "contamination", "distribution_pattern": "Distributed to Nevada for further distribution.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1222-2026" ], "product_short": "Zen Principle Naturals Moringa Leaf Powder", "product_count": 1, "slug": "2026-08-factory6", "title": "Zen Principle Naturals Moringa Leaf Powder Recall (August 2026): Reason, Lots, What to Do" }, { "event_id": "99419", "recalling_firm": "Mellish Island Corp", "city": "San Dimas", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-08-05", "recall_initiation_date": "2026-07-01", "reason_for_recall": "Firm's finished product label does not declare the source of marine collagen which was determined to be fish.", "category": "labeling", "distribution_pattern": "Product is distributed through TikTok exclusively. Presumably nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1190-2026" ], "product_short": "Mellish Island Super Skin", "product_count": 1, "slug": null }, { "event_id": "99317", "recalling_firm": "Total Nutrition Inc", "city": "Deer Park", "state": "NY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-07-29", "recall_initiation_date": "2026-06-26", "reason_for_recall": "Contaminated with Salmonella", "category": "contamination", "distribution_pattern": "nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1185-2026" ], "product_short": "TNVitamins 100% Organic Moringa Capsules", "product_count": 1, "slug": "2026-07-total-nutrition", "title": "TNVitamins 100% Organic Moringa Capsules Recall (July 2026): Reason, Lots, What to Do" }, { "event_id": "98304", "recalling_firm": "Modern Warrior Life, LLC", "city": "Scottsdale", "state": "AZ", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-07-29", "recall_initiation_date": "2026-01-09", "reason_for_recall": "FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.", "category": "tainted", "distribution_pattern": "The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1178-2026" ], "product_short": "Modern Warrior Ready", "product_count": 1, "slug": "2026-07-modern-warrior-life", "title": "Modern Warrior Ready Recall (July 2026): Reason, Lots, What to Do" }, { "event_id": "99294", "recalling_firm": "Provision Health Corp. dba PH Labs", "city": "San Diego", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-07-08", "recall_initiation_date": "2026-06-18", "reason_for_recall": "Dietary supplement product Ocular Plus contains undeclared Yellow#5.", "category": "labeling", "distribution_pattern": "Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "lutein-zeaxanthin", "omega-3" ], "products": [ "H-1134-2026", "H-1135-2026" ], "product_short": "Ocular Plus with Lutein", "product_count": 2, "slug": null }, { "event_id": "99071", "recalling_firm": "MOGO Moringa LLC", "city": "Saint Louis", "state": "MO", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-07-08", "recall_initiation_date": "2026-05-24", "reason_for_recall": "Product may be contaminated with Salmonella Typhimurium", "category": "contamination", "distribution_pattern": "Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1128-2026" ], "product_short": "MOGO PURE MORINGA OLEIFERA CAPSULES", "product_count": 1, "slug": "2026-07-mogo-moringa", "title": "MOGO PURE MORINGA OLEIFERA CAPSULES Recall (July 2026): Reason, Lots, What to Do" }, { "event_id": "99116", "recalling_firm": "SENSORY SUPPLEMENT LLC", "city": "Beverly Hills", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-06-17", "recall_initiation_date": "2026-05-06", "reason_for_recall": "Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.", "category": "other", "distribution_pattern": "Product is available nationwide and sold through the firm's online website direct to consumers.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "probiotics" ], "products": [ "H-1109-2026" ], "product_short": "NEURO NOURISH", "product_count": 1, "slug": null }, { "event_id": "99072", "recalling_firm": "Total Nutrition Inc", "city": "Deer Park", "state": "NY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-06-17", "recall_initiation_date": "2026-05-22", "reason_for_recall": "Product may be contaminated with Salmonella.", "category": "contamination", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0942-2026" ], "product_short": "TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules", "product_count": 1, "slug": "2026-06-total-nutrition", "title": "TNVitamins Ultrapotent Complete Green Superfood Recall (June 2026): Reason, Lots, What to Do" }, { "event_id": "98948", "recalling_firm": "Sato Pharmaceutical Inc.", "city": "Torrance", "state": "CA", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Ongoing", "report_date": "2026-06-10", "recall_initiation_date": "2026-03-12", "reason_for_recall": "Product does not meet label claim for Vitamin E.", "category": "labeling", "distribution_pattern": "Product was distributed to two domestic consignees who further distribute nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0892-2026" ], "product_short": "Yunker(branded) Energy & Health", "product_count": 1, "slug": null }, { "event_id": "98958", "recalling_firm": "Llorens Pharmaceuticals International Division, Inc.", "city": "Miami", "state": "FL", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-05-27", "recall_initiation_date": "2026-05-07", "reason_for_recall": "Foreign object: black particulate matter", "category": "contamination", "distribution_pattern": "Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b-complex", "methylfolate", "vitamin-c" ], "products": [ "H-0809-2026" ], "product_short": "Vitamin B-Complex", "product_count": 1, "slug": null }, { "event_id": "98663", "recalling_firm": "Blueroot Health, Inc.", "city": "Middletown", "state": "CT", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-04-15", "recall_initiation_date": "2026-03-27", "reason_for_recall": "Contains undeclared egg, soy, and hazelnut", "category": "allergen", "distribution_pattern": "Alaska, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, & Wyoming", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "bromelain", "vitamin-c" ], "products": [ "H-0663-2026" ], "product_short": "Vital Nutrients Aller-C", "product_count": 1, "slug": null }, { "event_id": "98592", "recalling_firm": "Pure Vitamins and Natural Supplements, LLC", "city": "Tampa", "state": "FL", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-04-15", "recall_initiation_date": "2026-03-13", "reason_for_recall": "FDA analysis revealed the presence of undeclared sildenafil", "category": "tainted", "distribution_pattern": "New Jersey", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0654-2026", "H-0655-2026" ], "product_short": "Blue Bull Extreme Male Enhancement Supplement", "product_count": 2, "slug": "2026-04-pure-vitamins-and-natural-supplements", "title": "Blue Bull Extreme Male Enhancement Supplement Recall (April 2026): Reason, Lots, What to Do" }, { "event_id": "97947", "recalling_firm": "Siluetaya, LLC", "city": "Albuquerque", "state": "NM", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-04-01", "recall_initiation_date": "2025-10-29", "reason_for_recall": "Product contains yellow oleander", "category": "tainted", "distribution_pattern": "Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0647-2026" ], "product_short": "SiluetaYa Mexican Tejocote Roots Supplement Pieces", "product_count": 1, "slug": "2026-04-siluetaya", "title": "SiluetaYa Mexican Tejocote Roots Supplement Pieces Recall (April 2026): Reason, Lots, What to Do" }, { "event_id": "98420", "recalling_firm": "Shaman Botanicals, LLC", "city": "North Kansas City", "state": "MO", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2026-03-25", "recall_initiation_date": "2026-02-13", "reason_for_recall": "A sample of the product had the active ingredient in a quantity greater than the labeled specification.", "category": "labeling", "distribution_pattern": "Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-1107-2026", "H-1108-2026" ], "product_short": "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS", "product_count": 2, "slug": null }, { "event_id": "98433", "recalling_firm": "Ambrosia Brands LLC", "city": "New York", "state": "NY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2026-03-18", "recall_initiation_date": "2026-02-13", "reason_for_recall": "Product may be contaminated with Salmonella", "category": "contamination", "distribution_pattern": "Nationwide in the United States, including American Samoa, Northern Mariana Islands, Puerto Rico, and Virgin Islands. International distribution to consumers in: Algeria, Anguilla, Australia, Austria, Bahrain, Belgium, Bosnia and Herzegovina, Brazil, Brunei, Bulgaria, Canada, Chile, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Djibouti, Dominican Republic, Egypt, Estonia, Faroe Islands, Finland, France, French Polynesia, Georgia, Germany, Gibraltar, Greece, Hong Kong, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Marshall Islands, Mexico, Nauru, New Zealand, Netherlands, Norway, Oman, Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Zimbabwe.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0546-2026" ], "product_short": "Rosabella MORINGA", "product_count": 1, "slug": null }, { "event_id": "98413", "recalling_firm": "Pure Solutions, Inc.", "city": "Tampa", "state": "FL", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2026-02-25", "recall_initiation_date": "2026-02-03", "reason_for_recall": "Label declares bovine colostrum but does not declare milk allergen.", "category": "allergen", "distribution_pattern": "Product was distributed to: AR, FL, CO, CA, CT, HI, IN, IL, ID, IA, KS, KY, LA, OH, OK, OR, MA, MI, MN, MO, GA, NC, NE, ND, NY, PA, SC, TN, NJ, UT, TX, VA , WA, WV, WI, WY", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0537-2026" ], "product_short": "Pure Factors Professional Nighttime Sleep Formula and Pure Formulas", "product_count": 1, "slug": null }, { "event_id": "98367", "recalling_firm": "Art Monkey LLC dba Why Not Natural", "city": "Houston", "state": "TX", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2026-02-25", "recall_initiation_date": "2026-01-28", "reason_for_recall": "Potential to be contaminated with Salmonella", "category": "contamination", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0510-2026" ], "product_short": "Why Not Natural Moringa Capsules", "product_count": 1, "slug": null }, { "event_id": "98325", "recalling_firm": "TKS Co-pack Manufacturing, LLC", "city": "Lindon", "state": "UT", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Completed", "report_date": "2026-02-18", "recall_initiation_date": "2026-01-15", "reason_for_recall": "Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.", "category": "contamination", "distribution_pattern": "Distributed to customer in Utah.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0520-2026", "H-0521-2026" ], "product_short": "Aonic Complete Hers", "product_count": 2, "slug": null }, { "event_id": "98082", "recalling_firm": "Imu-Tek Animal Health, Incorporated", "city": "Fort Collins", "state": "CO", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2026-02-11", "recall_initiation_date": "2025-11-25", "reason_for_recall": "Undeclared milk allergen", "category": "allergen", "distribution_pattern": "Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "colostrum" ], "products": [ "H-0483-2026" ], "product_short": "Imu-Tek Immuno-5 Colostrum Powder", "product_count": 1, "slug": null }, { "event_id": "98297", "recalling_firm": "SUPERFOODS, INC.", "city": "New York", "state": "NY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Completed", "report_date": "2026-02-04", "recall_initiation_date": "2026-01-15", "reason_for_recall": "Products may be contaminated with Salmonella Typhimurium", "category": "contamination", "distribution_pattern": "Nationwide, including Puerto Rico, Guam, and Virgin Islands; United Kingdom", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "spirulina" ], "products": [ "H-0433-2026", "H-0434-2026" ], "product_short": "Live it Up Super Greens", "product_count": 2, "slug": "2026-02-superfoods", "title": "Live it Up Super Greens Recall (February 2026): Reason, Lots, What to Do" }, { "event_id": "98267", "recalling_firm": "Herbs Forever", "city": "Los Angeles", "state": "CA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2026-01-21", "recall_initiation_date": "2026-01-06", "reason_for_recall": "Potential undeclared allergen ingredient (Wheat)", "category": "allergen", "distribution_pattern": "Product is sold primarily on-line nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0404-2026", "H-0405-2026" ], "product_short": "HerbsForever- Gastro Care", "product_count": 2, "slug": null }, { "event_id": "98037", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "category": "labeling", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "boswellia" ], "products": [ "H-0340-2026", "H-0341-2026", "H-0342-2026", "H-0343-2026", "H-0344-2026", "H-0345-2026", "H-0346-2026", "H-0347-2026", "H-0348-2026" ], "product_short": "Anti-virus", "product_count": 9, "slug": null }, { "event_id": "97893", "recalling_firm": "Avion Pharmaceuticals, LLC", "city": "Alpharetta", "state": "GA", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Ongoing", "report_date": "2025-12-10", "recall_initiation_date": "2025-10-29", "reason_for_recall": "Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.", "category": "allergen", "distribution_pattern": "Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, IA, IL, KY, MA, MO, NY, OH, OK, PA, TX & VA.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0233-2026" ], "product_short": "Prenate Chewable A chewable Rx prenatal vitamin with a delicious", "product_count": 1, "slug": null }, { "event_id": "97892", "recalling_firm": "Water Pure, Inc.", "city": "Plainview", "state": "NY", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-12-10", "recall_initiation_date": "2025-10-24", "reason_for_recall": "Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303", "category": "contamination", "distribution_pattern": "Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0213-2026" ], "product_short": "My Bladder", "product_count": 1, "slug": null }, { "event_id": "97885", "recalling_firm": "MeriCal, LLC", "city": "Anaheim", "state": "CA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2025-12-03", "recall_initiation_date": "2025-10-24", "reason_for_recall": "Potential contamination of Salmonella Richmond", "category": "contamination", "distribution_pattern": "Product was distributed to consignee locations across the country.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0205-2026" ], "product_short": "Member's Mark Super Greens", "product_count": 1, "slug": null }, { "event_id": "97552", "recalling_firm": "Professional Botanicals, Inc.", "city": "Ogden", "state": "UT", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-11-19", "recall_initiation_date": "2025-06-18", "reason_for_recall": "Products contains Magnesium Salicylate.", "category": "tainted", "distribution_pattern": "Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0181-2026", "H-0182-2026", "H-0183-2026" ], "product_short": "Nutra Calm", "product_count": 3, "slug": null }, { "event_id": "97608", "recalling_firm": "M.O.M Enterprises, LLC.", "city": "Richmond", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-12", "reason_for_recall": "Potential yeast contamination.", "category": "contamination", "distribution_pattern": "AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "elderberry", "vitamin-c" ], "products": [ "H-0025-2026" ], "product_short": "Organic BABY bedtime drops", "product_count": 1, "slug": null }, { "event_id": "97600", "recalling_firm": "Organicare Nature's Science, LLC", "city": "Austin", "state": "TX", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-04", "reason_for_recall": "Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.", "category": "contamination", "distribution_pattern": "Retail stores in all 50 states and Puerto Rico and via e-commerce", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0031-2026" ], "product_short": "FemiClear Daily Bladder Strength", "product_count": 1, "slug": null }, { "event_id": "97569", "recalling_firm": "New Spirit Naturals Inc.", "city": "San Dimas", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-03", "reason_for_recall": "undeclared allergen ingredient Milk.", "category": "allergen", "distribution_pattern": "Products are sold directly to consumers via firm's online website.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "glutathione" ], "products": [ "H-0020-2026" ], "product_short": "Gluta Plus (Glutathione)", "product_count": 1, "slug": null }, { "event_id": "97084", "recalling_firm": "Vitalabs, Inc.", "city": "McDonough", "state": "GA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Completed", "report_date": "2025-10-08", "recall_initiation_date": "2025-06-13", "reason_for_recall": "Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts.", "category": "allergen", "distribution_pattern": "Product was shipped to IL & NJ.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b12" ], "products": [ "H-0037-2026" ], "product_short": "vitamins B12", "product_count": 1, "slug": null }, { "event_id": "97500", "recalling_firm": "Extract Labs, Inc.", "city": "Lafayette", "state": "CO", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-10-01", "recall_initiation_date": "2025-08-26", "reason_for_recall": "Potential peanut protein cross-contact.", "category": "allergen", "distribution_pattern": "Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "elderberry" ], "products": [ "H-0621-2025", "H-0622-2025", "H-0623-2025", "H-0624-2025" ], "product_short": "Sugar-free Mixed Berry Gummies Name: Extract Labs Generic Name", "product_count": 4, "slug": null }, { "event_id": "97373", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "reason_for_recall": "Unapproved Drug Claims.", "category": "labeling", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "l-glutamine", "pine-bark-extract", "quercetin", "taurine" ], "products": [ "H-0586-2025", "H-0590-2025", "H-0591-2025", "H-0592-2025", "H-0593-2025", "H-0594-2025", "H-0595-2025", "H-0596-2025", "H-0597-2025", "H-0598-2025", "H-0599-2025", "H-0600-2025", "H-0601-2025" ], "product_short": "FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS", "product_count": 13, "slug": null }, { "event_id": "97401", "recalling_firm": "M.O.M Enterprises, LLC.", "city": "Richmond", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2025-09-17", "recall_initiation_date": "2025-08-05", "reason_for_recall": "Potential for spoilage due to yeast contamination.", "category": "contamination", "distribution_pattern": "AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "elderberry", "vitamin-c" ], "products": [ "H-0576-2025" ], "product_short": "Organic BABY bedtime drops", "product_count": 1, "slug": null }, { "event_id": "97377", "recalling_firm": "Dynamic Sports Nutrition", "city": "Humble", "state": "TX", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-09-17", "recall_initiation_date": "2025-07-28", "reason_for_recall": "Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.", "category": "labeling", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0573-2025" ], "product_short": "Anabolic Research WINN-50 (vanazolol)", "product_count": 1, "slug": null }, { "event_id": "97158", "recalling_firm": "GMP Laboratories of America Inc", "city": "Anaheim", "state": "CA", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-08-20", "recall_initiation_date": "2025-06-24", "reason_for_recall": "Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.", "category": "labeling", "distribution_pattern": "Distribution was to a single customer who received product in California and Oklahoma.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0447-2025", "H-0448-2025" ], "product_short": "Lithium Orotate 2.5", "product_count": 2, "slug": null }, { "event_id": "97062", "recalling_firm": "Vita Warehouse Corp.", "city": "Ronkonkoma", "state": "NY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2025-07-09", "recall_initiation_date": "2025-06-11", "reason_for_recall": "Contains undeclared peanut", "category": "allergen", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b12" ], "products": [ "H-0212-2025" ], "product_short": "Welby Vitamin B12 Adult Gummies", "product_count": 1, "slug": "2025-07-vita-warehouse", "title": "Welby Vitamin B12 Adult Gummies Recall (July 2025): Reason, Lots, What to Do" }, { "event_id": "96839", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "category": "labeling", "distribution_pattern": "Distributed Nationwide in the United States.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "iron" ], "products": [ "H-0091-2025", "H-0092-2025", "H-0093-2025", "H-0094-2025", "H-0095-2025", "H-0096-2025" ], "product_short": "Prothin", "product_count": 6, "slug": null }, { "event_id": "97056", "recalling_firm": "Yerba Prima Inc", "city": "Ashland", "state": "OR", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-06-25", "recall_initiation_date": "2025-06-10", "reason_for_recall": "Potential contamination with Pseudomonas aeruginosa.", "category": "contamination", "distribution_pattern": "Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "H-0050-2025" ], "product_short": "Great Plains Bentonite + Herbal Detox Capsules", "product_count": 1, "slug": null }, { "event_id": "96811", "recalling_firm": "NRC Nutrition Pty Ltd", "city": "Lytton", "state": "", "country": "Australia", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-06-18", "recall_initiation_date": "2025-03-29", "reason_for_recall": "inconsistent blending of iodine in the product", "category": "labeling", "distribution_pattern": "Texas, Minnesota, California, Indiana and Oklahoma", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0930-2025" ], "product_short": "Preconception Multi for Women", "product_count": 1, "slug": null }, { "event_id": "96689", "recalling_firm": "Nordic Naturals, Inc.", "city": "Watsonville", "state": "CA", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-06-11", "recall_initiation_date": "2025-05-02", "reason_for_recall": "Product is mislabeled.", "category": "labeling", "distribution_pattern": "Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "multivitamins" ], "products": [ "F-0840-2025" ], "product_short": "Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies", "product_count": 1, "slug": null }, { "event_id": "96749", "recalling_firm": "My Life Inc", "city": "Federal Way", "state": "WA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2025-05-28", "recall_initiation_date": "2025-04-25", "reason_for_recall": "Undeclared milk allergen", "category": "allergen", "distribution_pattern": "Sold to online consumers nationwide and distributed to Korea.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "lactoferrin" ], "products": [ "F-0807-2025" ], "product_short": "Lactoferrin as Apolactoferrin", "product_count": 1, "slug": "2025-05-my-life", "title": "Lactoferrin as Apolactoferrin Recall (May 2025): Reason, Lots, What to Do" }, { "event_id": "96713", "recalling_firm": "Optimal Carnivore, LLC", "city": "Cheyenne", "state": "WY", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2025-05-14", "recall_initiation_date": "2025-04-15", "reason_for_recall": "Potential for contamination with salmonella.", "category": "contamination", "distribution_pattern": "Nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0756-2025" ], "product_short": "Bone & Joint Restore", "product_count": 1, "slug": null }, { "event_id": "96657", "recalling_firm": "Supplement Manufacturing Partner Inc.", "city": "Largo", "state": "FL", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2025-04-30", "recall_initiation_date": "2025-04-04", "reason_for_recall": "Undeclared allergen: Wheat", "category": "allergen", "distribution_pattern": "Product was distributed throughout the United States and Germany.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "spermidine" ], "products": [ "F-0729-2025" ], "product_short": "Spermidine", "product_count": 1, "slug": "2025-04-supplement-manufacturing-partner", "title": "Spermidine Recall (April 2025): Reason, Lots, What to Do" }, { "event_id": "96578", "recalling_firm": "MTN OPS, LLC", "city": "Fruit Heights", "state": "UT", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-04-16", "recall_initiation_date": "2025-03-25", "reason_for_recall": "Undeclared soy flour", "category": "allergen", "distribution_pattern": "Distributed nationwide except RI and distributed in Canada", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "multivitamins" ], "products": [ "F-0698-2025" ], "product_short": "MTN OPS MULTI-V Men's Daily Multivitamin", "product_count": 1, "slug": null }, { "event_id": "96562", "recalling_firm": "Bioriginal Food & Science Corporation", "city": "Saskatoon", "state": "", "country": "Canada", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-04-09", "recall_initiation_date": "2025-03-21", "reason_for_recall": "Undeclared allergens: Soy lecithin", "category": "allergen", "distribution_pattern": "Puerto Rico", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "flaxseed-oil", "omega-3" ], "products": [ "F-0709-2025" ], "product_short": "Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil", "product_count": 1, "slug": null }, { "event_id": "96473", "recalling_firm": "Veridance Pharmacal, LLC", "city": "Springdale", "state": "AR", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-04-02", "recall_initiation_date": "2025-03-10", "reason_for_recall": "Levels of iodine exceeding label claim", "category": "labeling", "distribution_pattern": "One customer located in Gladstone, MO", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0671-2025" ], "product_short": "Omni-Macs McDonagh Medical Center", "product_count": 1, "slug": null }, { "event_id": "95959", "recalling_firm": "Vidaslim Co.", "city": "San Antonio", "state": "TX", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2025-02-12", "recall_initiation_date": "2024-12-11", "reason_for_recall": "Due to the presence of Toxic yellow oleander", "category": "tainted", "distribution_pattern": "These products were sold on a website and through direct sales via independent distributors throughout the USA.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0468-2025" ], "product_short": "VidaSlim 90-day", "product_count": 1, "slug": null }, { "event_id": "96054", "recalling_firm": "Iovate Health Sciences USA Inc.", "city": "Wilmington", "state": "DE", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-02-05", "recall_initiation_date": "2024-12-18", "reason_for_recall": "Presence of cathine in product", "category": "tainted", "distribution_pattern": "Domestic and foreign distribution:NC, CA, TX, NJ, VA, NV, PA, IN, NY, CA, IL,MS, KY, MI,SC, WA, CT, FL, OH, WI, DE, LA, TN, MO, UT, KH, GA, KS, CO, IA, AZ, OR. Foreign distribution: ZA, PH, IS, KZ, AE", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0455-2025" ], "product_short": "Alpha Test", "product_count": 1, "slug": null }, { "event_id": "96000", "recalling_firm": "Eclectic Institute Inc", "city": "Gresham", "state": "OR", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2025-01-22", "recall_initiation_date": "2022-08-03", "reason_for_recall": "Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel.", "category": "other", "distribution_pattern": "nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0401-2025" ], "product_short": "Eclectic Herb Vitamin Herb Blend vita biotic", "product_count": 1, "slug": null }, { "event_id": "95916", "recalling_firm": "Zoe US, Inc.", "city": "Canton", "state": "MA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2025-01-01", "recall_initiation_date": "2024-12-04", "reason_for_recall": "Product may contain foreign objects: small metal pieces and/or stones", "category": "contamination", "distribution_pattern": "Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Illinois, Kentucky, Maine, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0316-2025" ], "product_short": "ZOE Daily 30+ Prebiotic blend", "product_count": 1, "slug": null }, { "event_id": "95737", "recalling_firm": "Deseret Biologicals Inc", "city": "Sandy", "state": "UT", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-12-18", "recall_initiation_date": "2024-10-30", "reason_for_recall": "Product contains undeclared soy lecithin.", "category": "allergen", "distribution_pattern": "Distributed nationwide, one foreign distributor to Australia. No DOD distribution. No VA.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "phosphatidylserine" ], "products": [ "F-0262-2025" ], "product_short": "DesBio lunaSOMM Natural Sleep Support", "product_count": 1, "slug": null }, { "event_id": "95519", "recalling_firm": "Nestle Product Technology Center - Nestle Health Science", "city": "Bridgewater", "state": "NJ", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-11-27", "recall_initiation_date": "2024-10-07", "reason_for_recall": "Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot Numbers 50335944,50344396, expiration date 04/11/2026. The product is being recalled because of Incorrect formulation manufactured vs label claims. Product was manufactured with Niacin (as Nicotinic acid) and supplement facts panel states contains Niacin (as Niacinamide).", "category": "contamination", "distribution_pattern": "AK,AZ,CA,CO,DE,FL,GA,IA,ID,IL,IN,KS,KY,LA,MA,MD,MI,MN,MO,NC,NH,NJ,NM,NY,OH,OK,OR,PA,SD,TN,TX,VA,WA,WI,WV", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0139-2025" ], "product_short": "Douglas Labs Stress-B-Plus", "product_count": 1, "slug": null }, { "event_id": "95313", "recalling_firm": "Gorilla Mind LLC", "city": "Boise", "state": "ID", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2024-10-23", "recall_initiation_date": "2024-09-06", "reason_for_recall": "Product was recalled due to the potential for contamination with Salmonella", "category": "contamination", "distribution_pattern": "nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0053-2025" ], "product_short": "Gorilla Mind Rauwolscine", "product_count": 1, "slug": null }, { "event_id": "94762", "recalling_firm": "Penn Herb Company, Ltd.", "city": "Philadelphia", "state": "PA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2024-07-10", "recall_initiation_date": "2024-06-03", "reason_for_recall": "Potential Salmonella contamination", "category": "contamination", "distribution_pattern": "Distributed to customers in PA, CA, IL, FL, MI, MD, MO, OH, and NY.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1432-2024" ], "product_short": "Nature's Wonderland Thyroid Formula", "product_count": 1, "slug": null }, { "event_id": "94577", "recalling_firm": "Grato Holdings, Inc.", "city": "Woodbine", "state": "IA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-07-10", "recall_initiation_date": "2024-05-03", "reason_for_recall": "Potential microbial contamination (yeast and/or mold).", "category": "contamination", "distribution_pattern": "Nationwide US and Canada", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1458-2024", "F-1459-2024" ], "product_short": "Energique Mineral Magic", "product_count": 2, "slug": null }, { "event_id": "94346", "recalling_firm": "World Green Nutrition Inc.", "city": "San Antonio", "state": "TX", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2024-07-03", "recall_initiation_date": "2024-04-03", "reason_for_recall": "FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.", "category": "tainted", "distribution_pattern": "Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1391-2024" ], "product_short": "ELV Control", "product_count": 1, "slug": null }, { "event_id": "94438", "recalling_firm": "East West Tea Company, LLC", "city": "Eugene", "state": "OR", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2024-05-22", "recall_initiation_date": "2024-03-12", "reason_for_recall": "Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.", "category": "contamination", "distribution_pattern": "nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1237-2024" ], "product_short": "Organic Yogi Echinacea Immune Support", "product_count": 1, "slug": null }, { "event_id": "94230", "recalling_firm": "HTO Nevada Inc DBA Kirkman", "city": "Lake Oswego", "state": "OR", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2024-05-15", "recall_initiation_date": "2024-03-12", "reason_for_recall": "Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg).", "category": "labeling", "distribution_pattern": "Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "methylfolate" ], "products": [ "F-1222-2024" ], "product_short": "Kirkman 5-MTHF Methyltetrahydrofolate", "product_count": 1, "slug": null }, { "event_id": "93920", "recalling_firm": "HandNatural", "city": "San Luis", "state": "AZ", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Ongoing", "report_date": "2024-04-24", "recall_initiation_date": "2024-02-09", "reason_for_recall": "Product is being recalled due to the presence of yellow oleander and its components in the product.", "category": "tainted", "distribution_pattern": "Firm is 100% internet sales. Distribution is unknown at this time.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1158-2024", "F-1160-2024", "F-1161-2024" ], "product_short": "H&NATURAL TEJOCOTE ROOT", "product_count": 3, "slug": null }, { "event_id": "94226", "recalling_firm": "VRA FORMULATIONS LLC", "city": "Medley", "state": "FL", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2024-04-03", "recall_initiation_date": "2024-02-06", "reason_for_recall": "Due to sub-potent levels of Zinc", "category": "labeling", "distribution_pattern": "Domestic distribution only through internet sales.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1125-2024" ], "product_short": "TestoFREAK Maximize Testosterone", "product_count": 1, "slug": null }, { "event_id": "93947", "recalling_firm": "Nordic Naturals, Inc.", "city": "Watsonville", "state": "CA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-04-03", "recall_initiation_date": "2024-02-07", "reason_for_recall": "Elevated levels of vitamin D3", "category": "labeling", "distribution_pattern": "Products are distributed to 79 consignees, consisting of retailers, distributors, and consumers. Number of consignees who purchased through Amazon are unknown. U.S. distribution to AR, AZ, CA, DC, DE, FL, GA, IA, IL, IN, MA, MD, MI, MN, MO, MS, NC. ND, NH, NJ, NY, OH, OR, PA, RI, TX, VT and WI. Additionally, foreign customers in the Dubai and Kenya.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "vitamin-d" ], "products": [ "F-1109-2024" ], "product_short": "Nordic Naturals Baby s Vitamin D3 liquid", "product_count": 1, "slug": null }, { "event_id": "93899", "recalling_firm": "Ancient Formulas, Inc.", "city": "Wichita", "state": "KS", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2024-03-06", "recall_initiation_date": "2024-01-25", "reason_for_recall": "Product is sub-potent for Vitamin D and label contains incorrect percent daily value.", "category": "labeling", "distribution_pattern": "FL", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "vitamin-d" ], "products": [ "F-0930-2024" ], "product_short": "Healthprint Vitamin D3 5000", "product_count": 1, "slug": null }, { "event_id": "93774", "recalling_firm": "World Green Nutrition Inc.", "city": "San Antonio", "state": "TX", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2024-03-06", "recall_initiation_date": "2024-01-06", "reason_for_recall": "FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.", "category": "tainted", "distribution_pattern": "TX, CA, AZ, NC, GA, OR, WA, NM", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1000-2024" ], "product_short": "ELV ALIPOTEC MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE", "product_count": 1, "slug": null }, { "event_id": "93916", "recalling_firm": "The Procter & Gamble Company", "city": "Cincinnati", "state": "OH", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-02-28", "recall_initiation_date": "2024-02-01", "reason_for_recall": "Illegible Label", "category": "labeling", "distribution_pattern": "Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "psyllium" ], "products": [ "F-0907-2024" ], "product_short": "Meta Psyllium Fiber Capsules", "product_count": 1, "slug": null }, { "event_id": "93627", "recalling_firm": "Vita 360, LLC", "city": "San Juan", "state": "PR", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2024-01-17", "recall_initiation_date": "2023-12-07", "reason_for_recall": "FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.", "category": "labeling", "distribution_pattern": "Domestic distribution only throughout Puerto Rico", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0710-2024" ], "product_short": "SUPREX Plant Based Nutrition Carb & Sugar Block", "product_count": 1, "slug": null }, { "event_id": "93512", "recalling_firm": "BioMylz Pvt. Ltd.", "city": "Bengaluru", "state": "N/A", "country": "India", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2024-01-10", "recall_initiation_date": "2023-12-01", "reason_for_recall": "Potential mold contamination", "category": "contamination", "distribution_pattern": "Distributed to a distribution center in CA and then further distributed to distribution centers and retail stores nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "biotin", "collagen" ], "products": [ "F-0664-2024" ], "product_short": "Spring Valley Biotin & Collagen Liquid", "product_count": 1, "slug": null }, { "event_id": "93371", "recalling_firm": "LGNDS LLC", "city": "Miami", "state": "FL", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-12-20", "recall_initiation_date": "2023-10-13", "reason_for_recall": "Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.", "category": "tainted", "distribution_pattern": "U.S. distribution only.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0504-2024", "F-0505-2024" ], "product_short": "TYSON 2.0", "product_count": 2, "slug": null }, { "event_id": "93289", "recalling_firm": "Garden Of Life Llc", "city": "West Palm Beach", "state": "FL", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-12-13", "recall_initiation_date": "2023-10-19", "reason_for_recall": "Undeclared Soy.", "category": "allergen", "distribution_pattern": "Domestic and foreign distribution.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0482-2024", "F-0483-2024", "F-0484-2024" ], "product_short": "Garden of Life", "product_count": 3, "slug": null }, { "event_id": "93210", "recalling_firm": "ActiPharma, Inc.", "city": "Guaynabo", "state": "PR", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2023-11-29", "recall_initiation_date": "2023-09-28", "reason_for_recall": "FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.", "category": "labeling", "distribution_pattern": "Domestic distribution, in Puerto Rico.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0463-2024" ], "product_short": "ACTIRON", "product_count": 1, "slug": null }, { "event_id": "93157", "recalling_firm": "Kula Brands LLC", "city": "Naples", "state": "FL", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2023-11-15", "recall_initiation_date": "2023-09-21", "reason_for_recall": "Undeclared Allergens: Milk and Tree Nut (Coconut) and Unapproved Food Additive: Kratom", "category": "tainted", "distribution_pattern": "Domestic distribution only.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0320-2024" ], "product_short": "Kula Can Pina Colada + KRATOM SELTZER", "product_count": 1, "slug": null }, { "event_id": "93235", "recalling_firm": "Select Custom Solutions, LLC", "city": "La Crosse", "state": "WI", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-11-08", "recall_initiation_date": "2023-10-13", "reason_for_recall": "foreign material - plastic", "category": "contamination", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "protein" ], "products": [ "F-0313-2024" ], "product_short": "JayRobb Vanilla Flavored Egg White Protein Powder", "product_count": 1, "slug": null }, { "event_id": "92953", "recalling_firm": "Pharma-Natural Inc.", "city": "Miami Lakes", "state": "FL", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-15", "reason_for_recall": "FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.", "category": "other", "distribution_pattern": "Puerto Rico", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "biotin" ], "products": [ "F-1615-2023" ], "product_short": "Pharma Natural", "product_count": 1, "slug": null }, { "event_id": "92936", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "category": "contamination", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1547-2023", "F-1548-2023", "F-1549-2023", "F-1550-2023", "F-1551-2023", "F-1552-2023", "F-1553-2023", "F-1554-2023", "F-1555-2023", "F-1556-2023", "F-1557-2023", "F-1558-2023", "F-1559-2023", "F-1560-2023", "F-1561-2023", "F-1562-2023", "F-1563-2023", "F-1564-2023", "F-1565-2023", "F-1566-2023", "F-1567-2023", "F-1568-2023", "F-1569-2023", "F-1570-2023", "F-1571-2023", "F-1572-2023", "F-1573-2023", "F-1574-2023", "F-1575-2023", "F-1576-2023", "F-1577-2023", "F-1578-2023", "F-1579-2023", "F-1580-2023", "F-1581-2023", "F-1582-2023", "F-1583-2023", "F-1584-2023", "F-1585-2023", "F-1586-2023", "F-1587-2023", "F-1588-2023", "F-1589-2023", "F-1590-2023", "F-1591-2023", "F-1592-2023", "F-1593-2023", "F-1594-2023", "F-1595-2023", "F-1596-2023", "F-1597-2023", "F-1598-2023", "F-1599-2023", "F-1600-2023" ], "product_short": "100 vegetarian Fenugreek Capsules", "product_count": 54, "slug": null }, { "event_id": "92919", "recalling_firm": "OBC GROUP CORP", "city": "Doral", "state": "FL", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2023-09-27", "recall_initiation_date": "2023-09-05", "reason_for_recall": "Product appears to be Yellow Oleander instead of Nuez de la India as labeled.", "category": "tainted", "distribution_pattern": "Domestic distribution only.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1544-2023" ], "product_short": "NUT DIET MAX", "product_count": 1, "slug": null }, { "event_id": "92751", "recalling_firm": "Global Vitality Inc.", "city": "Chandler", "state": "AZ", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2023-08-23", "recall_initiation_date": "2023-07-13", "reason_for_recall": "potential contamination with E coli", "category": "contamination", "distribution_pattern": "Distributed to single consignee in California", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1442-2023", "F-1443-2023" ], "product_short": "Food Research International - Uro Kid Support Capsules", "product_count": 2, "slug": null }, { "event_id": "92685", "recalling_firm": "Emceta International Inc.", "city": "Doral", "state": "FL", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2023-08-02", "recall_initiation_date": "2023-07-10", "reason_for_recall": "FDA sample analysis of Natural Systems brand Multi Vitamin, 60 Tablets, found the magnesium content as 33.5% of the amount declared in label.", "category": "labeling", "distribution_pattern": "Domestic and Foreign distribution.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "multivitamins" ], "products": [ "F-1295-2023", "F-1296-2023" ], "product_short": "Natural Systems", "product_count": 2, "slug": null }, { "event_id": "92590", "recalling_firm": "International Food Companies DBA International Food Products", "city": "Hazelwood", "state": "MO", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-07-19", "recall_initiation_date": "2023-06-21", "reason_for_recall": "Product may contain Staphylococcus aureus.", "category": "contamination", "distribution_pattern": "MO", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-1246-2023", "F-1247-2023" ], "product_short": "1st phorm Level-1 Sustained Assimilation Protein", "product_count": 2, "slug": null }, { "event_id": "92385", "recalling_firm": "Procaps S.A. de C.V.", "city": "Soyapango", "state": "", "country": "El Salvador", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-06-14", "recall_initiation_date": "2023-05-19", "reason_for_recall": "PEG-40 not declared as an ingredient on the label", "category": "labeling", "distribution_pattern": "DE, TX, CA", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b12" ], "products": [ "F-0978-2023" ], "product_short": "Bacaolinita Liquid", "product_count": 1, "slug": null }, { "event_id": "92237", "recalling_firm": "Big Bold Health Holdings Inc", "city": "Bainbridge Island", "state": "WA", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-05-24", "recall_initiation_date": "2023-04-27", "reason_for_recall": "Glass fragments.", "category": "contamination", "distribution_pattern": "U.S. nationwide including Puerto Rico and to the following foreign countries: Australia, Canada, Sweden, Switzerland, and Taiwan.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0886-2023" ], "product_short": "Microbiome Rejuvenate", "product_count": 1, "slug": null }, { "event_id": "92162", "recalling_firm": "Euro-Pharma", "city": "Green Bay", "state": "WI", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2023-05-17", "recall_initiation_date": "2023-04-20", "reason_for_recall": "undeclared allergen (milk)", "category": "allergen", "distribution_pattern": "Nationwide", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b-complex", "b12", "methylfolate", "multivitamins" ], "products": [ "F-0841-2023" ], "product_short": "Multiple Vitamin B Capsules", "product_count": 1, "slug": null }, { "event_id": "92087", "recalling_firm": "FLP LLC", "city": "Tempe", "state": "AZ", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Ongoing", "report_date": "2023-05-17", "recall_initiation_date": "2023-03-29", "reason_for_recall": "Colostrum is declared but label does not declare milk.", "category": "allergen", "distribution_pattern": "Distributed in CA, FL, NJ, and NY.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "colostrum" ], "products": [ "F-0822-2023" ], "product_short": "Dr. Rico Perez Super Kids Colostrum", "product_count": 1, "slug": null }, { "event_id": "92070", "recalling_firm": "Novis PR, LLC dba Kramer Novis", "city": "San Juan", "state": "PR", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-05-10", "recall_initiation_date": "2023-03-27", "reason_for_recall": "Bloated Protein Bottle", "category": "other", "distribution_pattern": "Domestic distribution only.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0810-2023", "F-0811-2023", "F-0812-2023" ], "product_short": "GPre Protein", "product_count": 3, "slug": null }, { "event_id": "91571", "recalling_firm": "Natural Solutions Foundation", "city": "Newton", "state": "NJ", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-04-26", "recall_initiation_date": "2023-03-07", "reason_for_recall": "Product labeled and intended to mitigate, prevent, or treat COVID-19", "category": "labeling", "distribution_pattern": "Distributed to consumers nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0733-2023" ], "product_short": "Dr. Rima Recommends The Silver Solution Immune System Support", "product_count": 1, "slug": null }, { "event_id": "91155", "recalling_firm": "Mason Vitamins, Inc.", "city": "Miami Lakes", "state": "FL", "country": "United States", "classification": "Class III", "classifications": [ "Class III" ], "status": "Terminated", "report_date": "2023-03-22", "recall_initiation_date": "2022-11-14", "reason_for_recall": "Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.", "category": "labeling", "distribution_pattern": "Domestic distribution only.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "iron" ], "products": [ "F-0424-2023", "F-0425-2023" ], "product_short": "People's Choice Women's Daily Vitamins with Iron", "product_count": 2, "slug": null }, { "event_id": "91515", "recalling_firm": "Ortho Molecular Products, Inc.", "city": "Stevens Point", "state": "WI", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-02-15", "recall_initiation_date": "2023-01-12", "reason_for_recall": "Raw material tested positive for Cronobacter sakazakii.", "category": "contamination", "distribution_pattern": "Nationwide. Outside the US to Canada.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [], "products": [ "F-0340-2023" ], "product_short": "Fiber Powder", "product_count": 1, "slug": null }, { "event_id": "91377", "recalling_firm": "Professional Complementary Health Formulas, LLC", "city": "Lake Oswego", "state": "OR", "country": "United States", "classification": "Class II", "classifications": [ "Class II" ], "status": "Terminated", "report_date": "2023-02-08", "recall_initiation_date": "2021-12-20", "reason_for_recall": "Product recalled due to undeclared niacin.", "category": "labeling", "distribution_pattern": "Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "b-complex", "b12", "biotin", "calcium", "choline", "methylfolate", "myo-inositol", "vitamin-b6" ], "products": [ "F-0322-2023", "F-0323-2023" ], "product_short": "Inositol", "product_count": 2, "slug": null }, { "event_id": "91289", "recalling_firm": "THGH Partners, LLC", "city": "Calabasas", "state": "CA", "country": "United States", "classification": "Class I", "classifications": [ "Class I" ], "status": "Terminated", "report_date": "2023-01-11", "recall_initiation_date": "2022-12-05", "reason_for_recall": "Incorrect product label causing undeclared milk.", "category": "allergen", "distribution_pattern": "Product was sold online only in the United States, United Kingdom, Australia, New Zealand, Canada, and Mexico.", "voluntary_mandated": "Voluntary: Firm initiated", "ingredientSlugs": [ "calcium", "chromium", "digestive-enzymes", "protein", "vitamin-d" ], "products": [ "F-0216-2023" ], "product_short": "Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor", "product_count": 1, "slug": null } ], "recalls": [ { "recall_number": "H-1278-2026", "event_id": "99629", "report_date": "2026-09-02", "recall_initiation_date": "2026-08-11", "center_classification_date": "2026-08-26", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Byron White Formulas, Inc.", "city": "Santa Rosa", "state": "CA", "country": "United States", "product_description": "Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404", "product_short": "Byron White FORMULAS A-FNG", "reason_for_recall": "Label does not declare walnuts in English", "code_info": "Lot Code Format = MMD,DYY: 022,224. 061,424. 092,324. 022,125. 071,825. 112,125. 040,826.", "distribution_pattern": "Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.", "product_quantity": "10,403 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1278-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1277-2026", "event_id": "99629", "report_date": "2026-09-02", "recall_initiation_date": "2026-08-11", "center_classification_date": "2026-08-26", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Byron White Formulas, Inc.", "city": "Santa Rosa", "state": "CA", "country": "United States", "product_description": "Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404", "product_short": "Byron White FORMULAS A-P", "reason_for_recall": "Label does not declare walnuts in English", "code_info": "Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625.", "distribution_pattern": "Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.", "product_quantity": "3,486 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1277-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1276-2026", "event_id": "99629", "report_date": "2026-09-02", "recall_initiation_date": "2026-08-11", "center_classification_date": "2026-08-26", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Byron White Formulas, Inc.", "city": "Santa Rosa", "state": "CA", "country": "United States", "product_description": "Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404", "product_short": "Byron White FORMULAS A-L Complex", "reason_for_recall": "Label does not declare walnuts in English", "code_info": "Lot Code Format = MMD,DYY: 012,324. 041,924. 062,824. 092,024. 101,624. 111,324. 071,425. 093,025. 012,026. 042,826.", "distribution_pattern": "Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.", "product_quantity": "18,791 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1276-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1263-2026", "event_id": "98691", "report_date": "2026-09-02", "recall_initiation_date": "2026-04-03", "center_classification_date": "2026-08-24", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "ZMB Enterprises", "city": "Carlsbad", "state": "CA", "country": "United States", "product_description": "Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement", "product_short": "Addall XR Shot", "reason_for_recall": "The product contains 1,4-DMAA, Phenylethylamine and Phenibut.", "code_info": "Sold between July - December 2025", "distribution_pattern": "The firm markets their products online via their website addallxr.com", "product_quantity": "unknown", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": "2026-09-zmb-enterprises" }, { "recall_number": "H-1222-2026", "event_id": "99425", "report_date": "2026-08-12", "recall_initiation_date": "2026-07-19", "center_classification_date": "2026-08-05", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "FACTORY6, INC.", "city": "Lindon", "state": "UT", "country": "United States", "product_description": "Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP).", "product_short": "Zen Principle Naturals Moringa Leaf Powder", "reason_for_recall": "Possible Salmonella in Moringa Leaf Powder product.", "code_info": "LOT: A6FF4, Best By: 11/2028", "distribution_pattern": "Distributed to Nevada for further distribution.", "product_quantity": "2,048 bottles", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1222-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": "2026-08-factory6" }, { "recall_number": "H-1190-2026", "event_id": "99419", "report_date": "2026-08-05", "recall_initiation_date": "2026-07-01", "center_classification_date": "2026-07-28", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Mellish Island Corp", "city": "San Dimas", "state": "CA", "country": "United States", "product_description": "Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3", "product_short": "Mellish Island Super Skin", "reason_for_recall": "Firm's finished product label does not declare the source of marine collagen which was determined to be fish.", "code_info": "Lot: CA1G24 Expiration: 08-2027", "distribution_pattern": "Product is distributed through TikTok exclusively. Presumably nationwide.", "product_quantity": "1,600 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1190-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1185-2026", "event_id": "99317", "report_date": "2026-07-29", "recall_initiation_date": "2026-06-26", "center_classification_date": "2026-07-23", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Total Nutrition Inc", "city": "Deer Park", "state": "NY", "country": "United States", "product_description": "1. TNVitamins 100% Organic Moringa Capsules 1,200 mg\t 2. TNVitamins 100% Organic Moringa Powder 96 grams", "product_short": "TNVitamins 100% Organic Moringa Capsules", "reason_for_recall": "Contaminated with Salmonella", "code_info": "1. Product# AB9917 Lot #: 2800 Exp: 2/2028 2.Product# AB9904 Lot #: 2782 Exp: 5/2028", "distribution_pattern": "nationwide", "product_quantity": "8492 total units", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1185-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": "2026-07-total-nutrition" }, { "recall_number": "H-1178-2026", "event_id": "98304", "report_date": "2026-07-29", "recall_initiation_date": "2026-01-09", "center_classification_date": "2026-07-17", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Modern Warrior Life, LLC", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Modern Warrior Ready, Dietary Supplement, 60 CAPSULES", "product_short": "Modern Warrior Ready", "reason_for_recall": "FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.", "code_info": "Product distributed between April of 2022 until December 8th of 2025.", "distribution_pattern": "The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025", "product_quantity": "Unknown", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1178-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": "2026-07-modern-warrior-life" }, { "recall_number": "H-1135-2026", "event_id": "99294", "report_date": "2026-07-08", "recall_initiation_date": "2026-06-18", "center_classification_date": "2026-07-01", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Provision Health Corp. dba PH Labs", "city": "San Diego", "state": "CA", "country": "United States", "product_description": "Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023", "product_short": "Vista MAX", "reason_for_recall": "Dietary supplement product Vista MAX contains undeclared Yellow#5.", "code_info": "Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26", "distribution_pattern": "Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.", "product_quantity": "6,967 units across all lots", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1135-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1134-2026", "event_id": "99294", "report_date": "2026-07-08", "recall_initiation_date": "2026-06-18", "center_classification_date": "2026-07-01", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Provision Health Corp. dba PH Labs", "city": "San Diego", "state": "CA", "country": "United States", "product_description": "Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Serving Size: 4 Capsules; Distributed by: L.A. Farmacia Natural, Burbank, CA 91504 UPC: PHF-C023", "product_short": "Ocular Plus with Lutein", "reason_for_recall": "Dietary supplement product Ocular Plus contains undeclared Yellow#5.", "code_info": "Lots: 509011; 506013; 409012; Expiration: 09/27; 06/27; 09/26", "distribution_pattern": "Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.", "product_quantity": "6,967 units across all lots", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1134-2026%22", "category": "labeling", "ingredientSlugs": [ "lutein-zeaxanthin", "omega-3" ], "slug": null }, { "recall_number": "H-1128-2026", "event_id": "99071", "report_date": "2026-07-08", "recall_initiation_date": "2026-05-24", "center_classification_date": "2026-06-29", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "MOGO Moringa LLC", "city": "Saint Louis", "state": "MO", "country": "United States", "product_description": "MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132", "product_short": "MOGO PURE MORINGA OLEIFERA CAPSULES", "reason_for_recall": "Product may be contaminated with Salmonella Typhimurium", "code_info": "Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028", "distribution_pattern": "Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)", "product_quantity": "23,186 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1128-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": "2026-07-mogo-moringa" }, { "recall_number": "H-1109-2026", "event_id": "99116", "report_date": "2026-06-17", "recall_initiation_date": "2026-05-06", "center_classification_date": "2026-06-24", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "SENSORY SUPPLEMENT LLC", "city": "Beverly Hills", "state": "CA", "country": "United States", "product_description": "NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601", "product_short": "NEURO NOURISH", "reason_for_recall": "Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.", "code_info": "LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028", "distribution_pattern": "Product is available nationwide and sold through the firm's online website direct to consumers.", "product_quantity": "512 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1109-2026%22", "category": "other", "ingredientSlugs": [ "probiotics" ], "slug": null }, { "recall_number": "H-0942-2026", "event_id": "99072", "report_date": "2026-06-17", "recall_initiation_date": "2026-05-22", "center_classification_date": "2026-06-10", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Total Nutrition Inc", "city": "Deer Park", "state": "NY", "country": "United States", "product_description": "1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules)", "product_short": "TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules", "reason_for_recall": "Product may be contaminated with Salmonella.", "code_info": "1. Lot: 2507199 Exp. 09/2027 Lot: 2512-304 Exp. 02/2028 Lot: 2793 Exp. 02/2028 Lot: 2748 Exp. 07/2027 ASIN: B0DBRDPBDT, SKU: AB8047, UPC: 095234280472, FNSKU: X004C9XHAL 2. Lot: 2507199 Exp. 09/2027 Lot: 2748 Exp. 07/2027 UPC: 095234698734; SKU: AB9873", "distribution_pattern": "Nationwide", "product_quantity": "13,000 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0942-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": "2026-06-total-nutrition" }, { "recall_number": "H-0892-2026", "event_id": "98948", "report_date": "2026-06-10", "recall_initiation_date": "2026-03-12", "center_classification_date": "2026-06-02", "termination_date": null, "classification": "Class III", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Sato Pharmaceutical Inc.", "city": "Torrance", "state": "CA", "country": "United States", "product_description": "Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single UPC: 49873-916-11 3pack UPC: 49873-916-15 10pack UPC: 49873-916-07", "product_short": "Yunker(branded) Energy & Health", "reason_for_recall": "Product does not meet label claim for Vitamin E.", "code_info": "Lot: Expiration date: single CXW T Jan-27 3pack CXW T Jan-27 10pack PXW Z Mar-26 10pack XXW W Dec-27", "distribution_pattern": "Product was distributed to two domestic consignees who further distribute nationwide.", "product_quantity": "25,130 units across all package sizes", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0892-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0809-2026", "event_id": "98958", "report_date": "2026-05-27", "recall_initiation_date": "2026-05-07", "center_classification_date": "2026-05-19", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Llorens Pharmaceuticals International Division, Inc.", "city": "Miami", "state": "FL", "country": "United States", "product_description": "Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL", "product_short": "Vitamin B-Complex", "reason_for_recall": "Foreign object: black particulate matter", "code_info": "Lot: B2025 Expiration Date:08/27", "distribution_pattern": "Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE", "product_quantity": "4,196 units", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0809-2026%22", "category": "contamination", "ingredientSlugs": [ "b-complex", "vitamin-c", "methylfolate" ], "slug": null }, { "recall_number": "H-0663-2026", "event_id": "98663", "report_date": "2026-04-15", "recall_initiation_date": "2026-03-27", "center_classification_date": "2026-04-15", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Blueroot Health, Inc.", "city": "Middletown", "state": "CT", "country": "United States", "product_description": "Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles", "product_short": "Vital Nutrients Aller-C", "reason_for_recall": "Contains undeclared egg, soy, and hazelnut", "code_info": "100 count bottles - UPC: 693465524114,693465000083 Lot: 25E04-A, 25E04-B, 25E04 Expiration date: 05/27 200 count bottles - UPC:693465524213,693465000090 Lot: 25E04-B Expiration date: 05/27", "distribution_pattern": "Alaska, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, & Wyoming", "product_quantity": "11,849 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0663-2026%22", "category": "allergen", "ingredientSlugs": [ "vitamin-c", "bromelain" ], "slug": null }, { "recall_number": "H-0655-2026", "event_id": "98592", "report_date": "2026-04-15", "recall_initiation_date": "2026-03-13", "center_classification_date": "2026-04-07", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Pure Vitamins and Natural Supplements, LLC", "city": "Tampa", "state": "FL", "country": "United States", "product_description": "Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595", "product_short": "Red Bull Extreme Male Enhancement Supplement", "reason_for_recall": "FDA analysis revealed the presence of undeclared sildenafil", "code_info": "B/N ORB524 MFG Date: MAY 2024 EXP DATE: MAY 2029", "distribution_pattern": "New Jersey", "product_quantity": "Unknown", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0655-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": "2026-04-pure-vitamins-and-natural-supplements" }, { "recall_number": "H-0654-2026", "event_id": "98592", "report_date": "2026-04-15", "recall_initiation_date": "2026-03-13", "center_classification_date": "2026-04-07", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Pure Vitamins and Natural Supplements, LLC", "city": "Tampa", "state": "FL", "country": "United States", "product_description": "Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917", "product_short": "Blue Bull Extreme Male Enhancement Supplement", "reason_for_recall": "FDA analysis revealed the presence of undeclared sildenafil", "code_info": "EXP Date 02/2029", "distribution_pattern": "New Jersey", "product_quantity": "Unknown", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0654-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": "2026-04-pure-vitamins-and-natural-supplements" }, { "recall_number": "H-0647-2026", "event_id": "97947", "report_date": "2026-04-01", "recall_initiation_date": "2025-10-29", "center_classification_date": "2026-04-02", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Siluetaya, LLC", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 \" Expiration Date: 06/2027", "product_short": "SiluetaYa Mexican Tejocote Roots Supplement Pieces", "reason_for_recall": "Product contains yellow oleander", "code_info": "Lot: US1220, Expiration Date: 06/2027", "distribution_pattern": "Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT", "product_quantity": "40 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0647-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": "2026-04-siluetaya" }, { "recall_number": "H-1108-2026", "event_id": "98420", "report_date": "2026-03-25", "recall_initiation_date": "2026-02-13", "center_classification_date": "2026-06-24", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Shaman Botanicals, LLC", "city": "North Kansas City", "state": "MO", "country": "United States", "product_description": "Product label reads in part as \"WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801\"; Packaging: White child-resistant plastic bottle with sticker label applied UPC 810057763779 (sometimes proceeded by 00)", "product_short": "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS", "reason_for_recall": "A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.", "code_info": "B#AAW.501.3; all expiration dates", "distribution_pattern": "Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers", "product_quantity": "97,063 units", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1108-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-1107-2026", "event_id": "98420", "report_date": "2026-03-25", "recall_initiation_date": "2026-02-13", "center_classification_date": "2026-06-24", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Shaman Botanicals, LLC", "city": "North Kansas City", "state": "MO", "country": "United States", "product_description": "Product label reads in part as \"WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801\"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as \"WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801\"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724", "product_short": "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS", "reason_for_recall": "A sample of the product had the active ingredient in a quantity greater than the labeled specification.", "code_info": "B#AAW.501.3; all expiration dates", "distribution_pattern": "Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers", "product_quantity": "2 pack: 1281 units; 20-count: 14,491 units", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1107-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0546-2026", "event_id": "98433", "report_date": "2026-03-18", "recall_initiation_date": "2026-02-13", "center_classification_date": "2026-03-09", "termination_date": "2026-08-13", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Ambrosia Brands LLC", "city": "New York", "state": "NY", "country": "United States", "product_description": "Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min before a meal with an 8oz. glass of water or as directed by your health professional; UPC: 8 60012 16172 0", "product_short": "Rosabella MORINGA", "reason_for_recall": "Product may be contaminated with Salmonella", "code_info": "Lot # - Expiration Date: 5020591 - 03/2027 5020592 - 03/2027 5020593 - 03/2027 5020594 - 03/2027 5020595 - 03/2027 5020596 - 03/2027 5030246 - 04/2027 5030247 - 04/2027 5030248 - 04/2027 5030249 - 04/2027 5030250 - 04/2027 5030251 - 04/2027 5040270 - 05/2027 5040271 - 05/2027 5040272 - 05/2027 5040273 - 05/2027 5040274 - 05/2027 5040275 - 05/2027 5040276 - 05/2027 5040277 - 05/2027 5040278 - 05/2027 5040279 - 05/2027 5050053 - 6/2027 5050054 - 6/2027 5050055 - 6/2027 5050056 - 6/2027 5060069 - 07/2027 5060070 - 07/2027 5060071 - 07/2027 5060072 - 07/2027 5060073 - 07/2027 5060074 - 07/2027 5060075 - 07/2027 5060076 - 07/2027 5060077 - 07/2027 5060078 - 07/2027 5060079 - 07/2027 5060080 - 07/2027 5080084 - 9/2027 5080085 - 9/2027 5080086 - 9/2027 5090107 - 10/2027 5090108 - 10/2027 5090109 - 10/2027 5090113 - 10/2027 5090114 - 10/2027 5090115 - 10/2027 5090116 - 10/2027 5090117 - 10/2027 5090118 - 10/2027 5100039 - 11/2027 5100048 - 11/2027", "distribution_pattern": "Nationwide in the United States, including American Samoa, Northern Mariana Islands, Puerto Rico, and Virgin Islands. International distribution to consumers in: Algeria, Anguilla, Australia, Austria, Bahrain, Belgium, Bosnia and Herzegovina, Brazil, Brunei, Bulgaria, Canada, Chile, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Djibouti, Dominican Republic, Egypt, Estonia, Faroe Islands, Finland, France, French Polynesia, Georgia, Germany, Gibraltar, Greece, Hong Kong, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Marshall Islands, Mexico, Nauru, New Zealand, Netherlands, Norway, Oman, Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Zimbabwe.", "product_quantity": "1,224,208 units", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0546-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0537-2026", "event_id": "98413", "report_date": "2026-02-25", "recall_initiation_date": "2026-02-03", "center_classification_date": "2026-02-27", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Pure Solutions, Inc.", "city": "Tampa", "state": "FL", "country": "United States", "product_description": "Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)", "product_short": "Pure Factors Professional Nighttime Sleep Formula and Pure Formulas", "reason_for_recall": "Label declares bovine colostrum but does not declare milk allergen.", "code_info": "LOT: 0528D911 Expiration Date: May 2028", "distribution_pattern": "Product was distributed to: AR, FL, CO, CA, CT, HI, IN, IL, ID, IA, KS, KY, LA, OH, OK, OR, MA, MI, MN, MO, GA, NC, NE, ND, NY, PA, SC, TN, NJ, UT, TX, VA , WA, WV, WI, WY", "product_quantity": "442 units (bottles)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0537-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0510-2026", "event_id": "98367", "report_date": "2026-02-25", "recall_initiation_date": "2026-01-28", "center_classification_date": "2026-02-13", "termination_date": "2026-04-03", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Art Monkey LLC dba Why Not Natural", "city": "Houston", "state": "TX", "country": "United States", "product_description": "Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.", "product_short": "Why Not Natural Moringa Capsules", "reason_for_recall": "Potential to be contaminated with Salmonella", "code_info": "lot # A25G051", "distribution_pattern": "Nationwide", "product_quantity": "8,500 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0510-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0521-2026", "event_id": "98325", "report_date": "2026-02-18", "recall_initiation_date": "2026-01-15", "center_classification_date": "2026-02-20", "termination_date": null, "classification": "Class II", "status": "Completed", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "TKS Co-pack Manufacturing, LLC", "city": "Lindon", "state": "UT", "country": "United States", "product_description": "Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Sipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.", "product_short": "Aonic Complete His", "reason_for_recall": "Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.", "code_info": "Lot 5349A BB 12/27; Lot 5363A BB 12/27", "distribution_pattern": "Distributed to customer in Utah.", "product_quantity": "780 individual bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0521-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0520-2026", "event_id": "98325", "report_date": "2026-02-18", "recall_initiation_date": "2026-01-15", "center_classification_date": "2026-02-20", "termination_date": null, "classification": "Class II", "status": "Completed", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "TKS Co-pack Manufacturing, LLC", "city": "Lindon", "state": "UT", "country": "United States", "product_description": "Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Shipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.", "product_short": "Aonic Complete Hers", "reason_for_recall": "Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.", "code_info": "Lot 5349A BB 12/27; Lot 5363A BB 12/27", "distribution_pattern": "Distributed to customer in Utah.", "product_quantity": "3630 individual bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0520-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0483-2026", "event_id": "98082", "report_date": "2026-02-11", "recall_initiation_date": "2025-11-25", "center_classification_date": "2026-02-05", "termination_date": "2026-08-14", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Imu-Tek Animal Health, Incorporated", "city": "Fort Collins", "state": "CO", "country": "United States", "product_description": "Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for their pets).Packaging: Plastic jar with Sealed lid. Net Weight: 7 ounces. UPC:7 38654 00033 5 Firm name on label: Imu-Tek, 3541 East Vine Drive, Fort Collins, CO 80524", "product_short": "Imu-Tek Immuno-5 Colostrum Powder", "reason_for_recall": "Undeclared milk allergen", "code_info": "Lot #216, Expiration 4/16/2027", "distribution_pattern": "Distributed in : AZ, CA, CO, FL, MA, ME, MN, NC, NH, OK, RI, TN, TX, UT, and WI.", "product_quantity": "113 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0483-2026%22", "category": "allergen", "ingredientSlugs": [ "colostrum" ], "slug": null }, { "recall_number": "H-0434-2026", "event_id": "98297", "report_date": "2026-02-04", "recall_initiation_date": "2026-01-15", "center_classification_date": "2026-01-29", "termination_date": null, "classification": "Class I", "status": "Completed", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "SUPERFOODS, INC.", "city": "New York", "state": "NY", "country": "United States", "product_description": "a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 860013190811 b.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.32oz (9g) STICKS - NET WT. 9.52oz (270g); Manufactured for Superfoods, Inc.; UPC: 850077468070", "product_short": "Live it Up Super Greens", "reason_for_recall": "Products may be contaminated with Salmonella Typhimurium", "code_info": "The lot code is printed on the bottom back of the packaging in black and begins with the letter \"A\". Expiration dates from 08/2026 to 01/2028. 2024 Lots: A24G012, A24I036, A24J005, A24J032, A24J037, A24K028, A24L014, A24L019, A24L032 2025 Lots: A25A005, A25A058, A25B006, A25D010, A25D036, A25D041, A25E008, A25F021, A25H009, A25H030, A25H045, A25I011, A25J036, A25K035 Stick Pack Products: 32925-1, 34525-1", "distribution_pattern": "Nationwide, including Puerto Rico, Guam, and Virgin Islands; United Kingdom", "product_quantity": "795,834 units (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0434-2026%22", "category": "contamination", "ingredientSlugs": [ "spirulina" ], "slug": "2026-02-superfoods" }, { "recall_number": "H-0433-2026", "event_id": "98297", "report_date": "2026-02-04", "recall_initiation_date": "2026-01-15", "center_classification_date": "2026-01-29", "termination_date": null, "classification": "Class I", "status": "Completed", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "SUPERFOODS, INC.", "city": "New York", "state": "NY", "country": "United States", "product_description": "Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.28oz (8g) STICKS - NET WT. 8.47oz (240g); Manufactured for Superfoods, Inc.; UPC: 850077468063", "product_short": "Live it Up Super Greens", "reason_for_recall": "Products may be contaminated with Salmonella Typhimurium", "code_info": "The lot code is printed on the bottom back of the packaging in black and begins with the letter \"A\". Expiration dates from 08/2026 to 01/2028. 2024 Lots: AA24H013, A24I019, A24J012, A24J041, A24K019, A24L001, A24L013, A24L036, A24L035 2025 Lots: A25A009, A25A017, A25A018, A25B005, A25B004, A25C018, A25C022, A25D021, A25E005, A25E007, A25F019, A25G033, A25F029, A25G065, A25H005, A25H012, A25I005, A25I010, A25I032, A25J005, A25J028, A25J037, A25K007, A25K013, A25L006 Stick Pack Products: 32825-1, 34425-1", "distribution_pattern": "Nationwide, including Puerto Rico, Guam, and Virgin Islands; United Kingdom", "product_quantity": "795,834 units (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0433-2026%22", "category": "contamination", "ingredientSlugs": [ "spirulina" ], "slug": "2026-02-superfoods" }, { "recall_number": "H-0405-2026", "event_id": "98267", "report_date": "2026-01-21", "recall_initiation_date": "2026-01-06", "center_classification_date": "2026-01-14", "termination_date": "2026-05-05", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Herbs Forever", "city": "Los Angeles", "state": "CA", "country": "United States", "product_description": "HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4", "product_short": "HerbsForever- Hingwastika Churna", "reason_for_recall": "Potential undeclared allergen ingredient (Wheat)", "code_info": "Batch: 622-2 Expiration date: 6/2029", "distribution_pattern": "Product is sold primarily on-line nationwide.", "product_quantity": "45 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0405-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0404-2026", "event_id": "98267", "report_date": "2026-01-21", "recall_initiation_date": "2026-01-06", "center_classification_date": "2026-01-14", "termination_date": "2026-05-05", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Herbs Forever", "city": "Los Angeles", "state": "CA", "country": "United States", "product_description": "HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3", "product_short": "HerbsForever- Gastro Care", "reason_for_recall": "Potential undeclared allergen ingredient (Wheat)", "code_info": "Batch: 124-4 Expiration date: 1/2029", "distribution_pattern": "Product is sold primarily on-line nationwide.", "product_quantity": "45 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0404-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0348-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag", "product_short": "Sinus Cap", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "38 bags", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0348-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0347-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537", "product_short": "Pain Away", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "275 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0347-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0346-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag", "product_short": "Organic Ginger Root", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "48 bags", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0346-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0345-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle", "product_short": "Ear Drops", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "T553MF EXP 12/28", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "22 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0345-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0344-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831", "product_short": "Chaga Mushroom", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "144 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0344-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0343-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420", "product_short": "Boswellia", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "278 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0343-2026%22", "category": "labeling", "ingredientSlugs": [ "boswellia" ], "slug": null }, { "recall_number": "H-0342-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle", "product_short": "Baby Soothe", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "E164BS EXP 1/27 E128BS EXP 7/26", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "49 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0342-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0341-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282", "product_short": "Baby Allergy", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "E166SA EXP 4/28", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "23 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0341-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0340-2026", "event_id": "98037", "report_date": "2025-12-31", "recall_initiation_date": "2025-11-20", "center_classification_date": "2025-12-23", "termination_date": "2026-08-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "A New Life Herbs, LLC", "city": "Somerville", "state": "TN", "country": "United States", "product_description": "Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429", "product_short": "Anti-virus", "reason_for_recall": "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label", "code_info": "T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28", "distribution_pattern": "AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN", "product_quantity": "116 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0340-2026%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0233-2026", "event_id": "97893", "report_date": "2025-12-10", "recall_initiation_date": "2025-10-29", "center_classification_date": "2025-12-03", "termination_date": null, "classification": "Class III", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Avion Pharmaceuticals, LLC", "city": "Alpharetta", "state": "GA", "country": "United States", "product_description": "Prenate Chewable A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic Dietary Supplement 30 Tablets Rx Only UPC 3 75854 30630 2 Manufactured for: Avion Pharmaceuticals, LLC Alpharetta, GA 30005", "product_short": "Prenate Chewable A chewable Rx prenatal vitamin with a delicious", "reason_for_recall": "Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.", "code_info": "Product Code 75854-306-30 Lot 2402036 Exp 2026-04 Lot 2402036A Exp 2026-04 & Lot 2412020 Exp 2027-02", "distribution_pattern": "Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, IA, IL, KY, MA, MO, NY, OH, OK, PA, TX & VA.", "product_quantity": "804 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0233-2026%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0213-2026", "event_id": "97892", "report_date": "2025-12-10", "recall_initiation_date": "2025-10-24", "center_classification_date": "2025-11-28", "termination_date": "2026-04-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Water Pure, Inc.", "city": "Plainview", "state": "NY", "country": "United States", "product_description": "My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap; bottle size is 150 CC; the net contents in 60 clear capsules containing brown powder", "product_short": "My Bladder", "reason_for_recall": "Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303", "code_info": "Lot Number: 03042517", "distribution_pattern": "Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada", "product_quantity": "17,612 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0213-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0205-2026", "event_id": "97885", "report_date": "2025-12-03", "recall_initiation_date": "2025-10-24", "center_classification_date": "2025-11-21", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "MeriCal, LLC", "city": "Anaheim", "state": "CA", "country": "United States", "product_description": "Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775", "product_short": "Member's Mark Super Greens", "reason_for_recall": "Potential contamination of Salmonella Richmond", "code_info": "500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;", "distribution_pattern": "Product was distributed to consignee locations across the country.", "product_quantity": "698,064 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0205-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0183-2026", "event_id": "97552", "report_date": "2025-11-19", "recall_initiation_date": "2025-06-18", "center_classification_date": "2025-11-12", "termination_date": "2025-12-31", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Professional Botanicals, Inc.", "city": "Ogden", "state": "UT", "country": "United States", "product_description": "Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207", "product_short": "Tense-X", "reason_for_recall": "Products contains Magnesium Salicylate.", "code_info": "Lot #: 290301", "distribution_pattern": "Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.", "product_quantity": "253 Bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0183-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0182-2026", "event_id": "97552", "report_date": "2025-11-19", "recall_initiation_date": "2025-06-18", "center_classification_date": "2025-11-12", "termination_date": "2025-12-31", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Professional Botanicals, Inc.", "city": "Ogden", "state": "UT", "country": "United States", "product_description": "Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.", "product_short": "Total Comfort", "reason_for_recall": "Products contains Magnesium Salicylate.", "code_info": "Lot #: 280914", "distribution_pattern": "Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.", "product_quantity": "430 Bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0182-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0181-2026", "event_id": "97552", "report_date": "2025-11-19", "recall_initiation_date": "2025-06-18", "center_classification_date": "2025-11-12", "termination_date": "2025-12-31", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Professional Botanicals, Inc.", "city": "Ogden", "state": "UT", "country": "United States", "product_description": "Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku: PB248", "product_short": "Nutra Calm", "reason_for_recall": "Products contains Magnesium Salicylate.", "code_info": "Lot #: 71527", "distribution_pattern": "Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.", "product_quantity": "452 Bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0181-2026%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0031-2026", "event_id": "97600", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-04", "center_classification_date": "2025-10-09", "termination_date": "2026-01-14", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Organicare Nature's Science, LLC", "city": "Austin", "state": "TX", "country": "United States", "product_description": "FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060", "product_short": "FemiClear Daily Bladder Strength", "reason_for_recall": "Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.", "code_info": "Lot 111924176", "distribution_pattern": "Retail stores in all 50 states and Puerto Rico and via e-commerce", "product_quantity": "15,075 bottles (28 ct per bottle)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0031-2026%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0025-2026", "event_id": "97608", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-12", "center_classification_date": "2025-10-07", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "M.O.M Enterprises, LLC.", "city": "Richmond", "state": "CA", "country": "United States", "product_description": "Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)", "product_short": "Organic BABY bedtime drops", "reason_for_recall": "Potential yeast contamination.", "code_info": "Lot code: 25100, 25148, 25155 UPC: 679234051814 EXP 04/2027, 05/2027, 06/2027", "distribution_pattern": "AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI", "product_quantity": "46,752 units/bottles (Lot 25100: 8,424 units; Lot 25148: 16,488 units; Lot 25155: 21,840 units)", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0025-2026%22", "category": "contamination", "ingredientSlugs": [ "elderberry", "vitamin-c" ], "slug": null }, { "recall_number": "H-0020-2026", "event_id": "97569", "report_date": "2025-10-15", "recall_initiation_date": "2025-09-03", "center_classification_date": "2025-10-06", "termination_date": "2026-04-23", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "New Spirit Naturals Inc.", "city": "San Dimas", "state": "CA", "country": "United States", "product_description": "Gluta Plus (Glutathione) 60 capsules/container. UPC: NA", "product_short": "Gluta Plus (Glutathione)", "reason_for_recall": "undeclared allergen ingredient Milk.", "code_info": "Lot codes: 231101V; 231142V; 241773V; 243381V", "distribution_pattern": "Products are sold directly to consumers via firm's online website.", "product_quantity": "83 units", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0020-2026%22", "category": "allergen", "ingredientSlugs": [ "glutathione" ], "slug": null }, { "recall_number": "H-0037-2026", "event_id": "97084", "report_date": "2025-10-08", "recall_initiation_date": "2025-06-13", "center_classification_date": "2025-10-10", "termination_date": null, "classification": "Class II", "status": "Completed", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitalabs, Inc.", "city": "McDonough", "state": "GA", "country": "United States", "product_description": "vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gummies UPC 8 60008 57505 0 Manufactured for: Black Girl Vitamins 601 W Harrison St., Chicago, IL 60607. 2. Rise-N-Shine 17 Woodport Road, Sparta, NJ 07871 UPC 8 99130 01189 1", "product_short": "vitamins B12", "reason_for_recall": "Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts.", "code_info": "1. LOT# 57221A BEST BY: 07/2026 and Lot# 56199 Best By: 07/2026 2. Lot# 57664 Best By: 07/2026", "distribution_pattern": "Product was shipped to IL & NJ.", "product_quantity": "9,657 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0037-2026%22", "category": "allergen", "ingredientSlugs": [ "b12" ], "slug": null }, { "recall_number": "H-0624-2025", "event_id": "97500", "report_date": "2025-10-01", "recall_initiation_date": "2025-08-26", "center_classification_date": "2025-09-22", "termination_date": "2025-10-30", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Extract Labs, Inc.", "city": "Lafayette", "state": "CO", "country": "United States", "product_description": "Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)", "product_short": "Mai Tai", "reason_for_recall": "Potential peanut protein cross-contact.", "code_info": "Lot: 25JD042507A EXP: 07/2027 Printed on bulk bag identifier adhesive", "distribution_pattern": "Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.", "product_quantity": "19,750 gummies", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0624-2025%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0623-2025", "event_id": "97500", "report_date": "2025-10-01", "recall_initiation_date": "2025-08-26", "center_classification_date": "2025-09-22", "termination_date": "2025-10-30", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Extract Labs, Inc.", "city": "Lafayette", "state": "CO", "country": "United States", "product_description": "Blue Razz 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Blue Razz: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)", "product_short": "Blue Razz", "reason_for_recall": "Potential peanut protein cross-contact.", "code_info": "Lot: 25JD082307A EXP: 07/2027 Printed on bulk bag identifier adhesive", "distribution_pattern": "Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.", "product_quantity": "19,810 gummies", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0623-2025%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0622-2025", "event_id": "97500", "report_date": "2025-10-01", "recall_initiation_date": "2025-08-26", "center_classification_date": "2025-09-22", "termination_date": "2025-10-30", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Extract Labs, Inc.", "city": "Lafayette", "state": "CO", "country": "United States", "product_description": "Elderberry 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Elderberry: 24 bags x 5kg and 1 bag x 3.6kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)", "product_short": "Elderberry", "reason_for_recall": "Potential peanut protein cross-contact.", "code_info": "Lot: 25JD072107A EXP: 07/2027 Printed on bulk bag identifier adhesive", "distribution_pattern": "Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.", "product_quantity": "19,720 gummies", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0622-2025%22", "category": "allergen", "ingredientSlugs": [ "elderberry" ], "slug": null }, { "recall_number": "H-0621-2025", "event_id": "97500", "report_date": "2025-10-01", "recall_initiation_date": "2025-08-26", "center_classification_date": "2025-09-22", "termination_date": "2025-10-30", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Extract Labs, Inc.", "city": "Lafayette", "state": "CO", "country": "United States", "product_description": "Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use: Dietary Supplement Type of packaging: 225cc amber packer bottle with child-resistant cap and inner pressure seal Net wt: 3.53oz UPC: 850029647928 Firm name & address: Extract Labs, Inc., 1399 Horizon Ave, Lafayette, CO 80026", "product_short": "Sugar-free Mixed Berry Gummies Name: Extract Labs Generic Name", "reason_for_recall": "Potential peanut protein cross-contact.", "code_info": "Lot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle", "distribution_pattern": "Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.", "product_quantity": "2180 gummies (109/20 ct bottles)", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0621-2025%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0601-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT WATERMELON NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40905 6 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071", "product_short": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot 174271126 Exp Date 09/26", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0601-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0600-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT PEACH MANGO NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40906 3 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071", "product_short": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot 202140114 Exp Date 03/27", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0600-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0599-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 veggie caps DIETARY SUPPLEMENT UPC 8 11226 02158 4 Distributed by: TOP SECRET NUTRITION, LLC 6015-B Unity Dr. Norcross, GA 30052", "product_short": "Top Secret Nutrition extra strength uric control fast acting", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot C1238 Exp Date 01/25", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0599-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0598-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN ANTIOXIDANT PROPERTIES SUPPORTS HEALTHY BLOOD SUGAR LEVELS NET WT. 8.12OZ (250g) DIETARY SUPPLEMENT UPC 6 89466 70601 7 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071", "product_short": "PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot 710581618 Exp Date 12/26", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0598-2025%22", "category": "labeling", "ingredientSlugs": [ "taurine" ], "slug": null }, { "recall_number": "H-0597-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT KIWI-STRAWBERRY NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 89466 70619 2 Manufactured by: Prime Nutrition 6015-b Unity Drive Norcross, GA 30071", "product_short": "PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot 207460659 Exp Date 10/25", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0597-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0596-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEMENT 17-PROANDRO pBOLD FORM-XT UPC 7 44890 94151 6 MADE FOR LG SCIENCES 6015-B UNITY DR. NORCROXX, GA 30071", "product_short": "LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot Cl 78216691877 Exp Date 02/28", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0596-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0595-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54503 00226 5 Manufactured By: iForce Nutrition 6015B Unity Drive Norcross, GA 30071", "product_short": "IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot 101330812 Exp Date 01/25", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0595-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0594-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071", "product_short": "HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot C1612 Exp Date 08/27", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0594-2025%22", "category": "labeling", "ingredientSlugs": [ "quercetin" ], "slug": null }, { "recall_number": "H-0593-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEPTOR AGONIST 180 TABLETS DIETARY SUPPLEMENT", "product_short": "HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot C19El8 Exp Date 05/30", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0593-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0592-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION SUPPORTS CARDIOVASCULAR HEALTH FIGHTS OXIDATIVE STRESS 60 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02446 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071", "product_short": "HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION", "reason_for_recall": "Unapproved Drug Claims and Misbranded.", "code_info": "Lot C15Cl4 Exp Date 10/26", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0592-2025%22", "category": "labeling", "ingredientSlugs": [ "pine-bark-extract" ], "slug": null }, { "recall_number": "H-0591-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH PHARMECEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071", "product_short": "HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot 059960809 Exp Date 06/28", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0591-2025%22", "category": "labeling", "ingredientSlugs": [ "l-glutamine" ], "slug": null }, { "recall_number": "H-0590-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071", "product_short": "HI-TECH PHARMACEUTICALS JOINT-RX", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot 503110607 Exp Date 04/30", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0590-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0586-2025", "event_id": "97373", "report_date": "2025-09-24", "recall_initiation_date": "2025-08-06", "center_classification_date": "2025-09-12", "termination_date": "2026-02-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Hi-Tech Pharmaceuticals Inc.", "city": "Norcross", "state": "GA", "country": "United States", "product_description": "FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH CARTILAGE LUBRICATES JOINTS 240 Capsules UPC 7 97573 90884 1 6015-B Unity Drive Norcross, GA 30071", "product_short": "FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS", "reason_for_recall": "Unapproved Drug Claims.", "code_info": "Lot 405310805 Exp Date 07/28", "distribution_pattern": "Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.", "product_quantity": "85,950 units total", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0586-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0576-2025", "event_id": "97401", "report_date": "2025-09-17", "recall_initiation_date": "2025-08-05", "center_classification_date": "2025-09-08", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "M.O.M Enterprises, LLC.", "city": "Richmond", "state": "CA", "country": "United States", "product_description": "Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)", "product_short": "Organic BABY bedtime drops", "reason_for_recall": "Potential for spoilage due to yeast contamination.", "code_info": "Lot code: 25084; 25086; UPC: 679234051814 EXP 03/2027", "distribution_pattern": "AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI", "product_quantity": "85,248 units/bottles (Lot 25084: 51,096 units; Lot 25086: 34,152 units)", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0576-2025%22", "category": "contamination", "ingredientSlugs": [ "elderberry", "vitamin-c" ], "slug": null }, { "recall_number": "H-0573-2025", "event_id": "97377", "report_date": "2025-09-17", "recall_initiation_date": "2025-07-28", "center_classification_date": "2025-09-05", "termination_date": "2026-02-06", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Dynamic Sports Nutrition", "city": "Humble", "state": "TX", "country": "United States", "product_description": "Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured For: Anabolic Research, 6942 FM 1960 E. #346, Humble, TX 77346-2706.", "product_short": "Anabolic Research WINN-50 (vanazolol)", "reason_for_recall": "Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.", "code_info": "LOT: 2307149 MFG: 07/2023", "distribution_pattern": "Nationwide", "product_quantity": "1,566 bottles -2.4 oz each", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0573-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0448-2025", "event_id": "97158", "report_date": "2025-08-20", "recall_initiation_date": "2025-06-24", "center_classification_date": "2025-08-08", "termination_date": "2026-02-24", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "GMP Laboratories of America Inc", "city": "Anaheim", "state": "CA", "country": "United States", "product_description": "Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661", "product_short": "Lithium Orotate", "reason_for_recall": "Downstream recall of a dietary supplement ingredient that was manufactured out of specification.", "code_info": "2.5mg Lot #: 21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09/2026, 05/2027, 02/2028 5 mg Lot#: 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718 Expire date: 10/2025, 05/2026, 08/2026, 01/2027, 04/2027, 05/2027, 08/2027, 02/2028 10mg Lot#: 21107, 21181, 21288, 21371, 21499, 21695, 21993, 22105, 22200, 22399, 22556, 22650, 22736 Expire date: 10/2025, 12/2025, 02/2026, 03/2026, 05/2026, 07/2026, 01/2027, 01/2027, 03/2027, 07/2027, 10/2027, 01/2028, 02/2029 20mg Lot#: 21301, 21505, 21911, 22106, 22257, 22397, 22557, 22918 Expire date: 02/2026, 05/2026, 10/2026, 05/2027, 07/2028, 10/2027, 04/2028 1000 MCG Lot#: 21442, 22647 Expire date: 05/2025, 01/2027", "distribution_pattern": "Distribution was to a single customer who received product in California and Oklahoma.", "product_quantity": "~185,482 capsules", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0448-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0447-2025", "event_id": "97158", "report_date": "2025-08-20", "recall_initiation_date": "2025-06-24", "center_classification_date": "2025-08-08", "termination_date": "2026-02-24", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "GMP Laboratories of America Inc", "city": "Anaheim", "state": "CA", "country": "United States", "product_description": "Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405, San Fransisco, CA 94108 2.5 mg UPC#: X002T4OPLL 10 mg UPC#: X0031AXVE9", "product_short": "Lithium Orotate 2.5", "reason_for_recall": "Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.", "code_info": "2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028", "distribution_pattern": "Distribution was to a single customer who received product in California and Oklahoma.", "product_quantity": "~185,482 capsules", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0447-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0212-2025", "event_id": "97062", "report_date": "2025-07-09", "recall_initiation_date": "2025-06-11", "center_classification_date": "2025-07-03", "termination_date": "2025-10-28", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vita Warehouse Corp.", "city": "Ronkonkoma", "state": "NY", "country": "United States", "product_description": "1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe\" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count", "product_short": "Welby Vitamin B12 Adult Gummies", "reason_for_recall": "Contains undeclared peanut", "code_info": "1. UPC Code: 4099100290868 Lot #: 248046601 Expiration Date: 10/2026 2. UPC Code: 888670132487 Lot #: 248046601 Expiration Date: 10/2026 3. UPC Code: 850005214670 Lot #: 248046601 Expiration Date: 10/2026 4. Lot# 248046601 Expiration date: 10/2026", "distribution_pattern": "Nationwide", "product_quantity": "40,522 bottles plus 582,000 individual gummies", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0212-2025%22", "category": "allergen", "ingredientSlugs": [ "b12" ], "slug": "2025-07-vita-warehouse" }, { "recall_number": "H-0096-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "Rodex Forte", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "Batch codes: 21635-21, 21635-22, 21635-23, 21635-34", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "42,280 capsules", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0096-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0095-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "NutriLean", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "21745-11, 21745-12, 21745-13, 21745-14, 21745-15", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "94,190 capsules", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0095-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0094-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "Probese Caps", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "21874-19; 21874-20; 21874-21; 21874-22; 21874-23; 21874-24; 21874-25", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "112,506 pills", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0094-2025%22", "category": "labeling", "ingredientSlugs": [ "iron" ], "slug": null }, { "recall_number": "H-0093-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Protrim Plus, dietary supplement. 90 capsule/bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "Protrim Plus", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "21634-9", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "763 Containers", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0093-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0092-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "Super ProTHIN Plus", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "12131", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "55,080 pills", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0092-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0091-2025", "event_id": "96839", "report_date": "2025-07-02", "recall_initiation_date": "2025-04-30", "center_classification_date": "2025-06-25", "termination_date": "2025-09-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Preventics, Inc. dba Legere Pharmaceuticals", "city": "Scottsdale", "state": "AZ", "country": "United States", "product_description": "Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)", "product_short": "Prothin", "reason_for_recall": "Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.", "code_info": "12131", "distribution_pattern": "Distributed Nationwide in the United States.", "product_quantity": "1696 bags", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0091-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "H-0050-2025", "event_id": "97056", "report_date": "2025-06-25", "recall_initiation_date": "2025-06-10", "center_classification_date": "2025-06-17", "termination_date": "2025-09-05", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Yerba Prima Inc", "city": "Ashland", "state": "OR", "country": "United States", "product_description": "Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA", "product_short": "Great Plains Bentonite + Herbal Detox Capsules", "reason_for_recall": "Potential contamination with Pseudomonas aeruginosa.", "code_info": "Lot # 05051, Expiration Date 02/2028. Lot code breaks down as follows: 050 = 3 digits pertaining to the day of the year 5 = last number of the year 2025 1 = number of batch records issued of the day", "distribution_pattern": "Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.", "product_quantity": "4985 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0050-2025%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0930-2025", "event_id": "96811", "report_date": "2025-06-18", "recall_initiation_date": "2025-03-29", "center_classification_date": "2025-06-09", "termination_date": "2026-07-01", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "NRC Nutrition Pty Ltd", "city": "Lytton", "state": "", "country": "Australia", "product_description": "Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469", "product_short": "Preconception Multi for Women", "reason_for_recall": "inconsistent blending of iodine in the product", "code_info": "Batch 42469", "distribution_pattern": "Texas, Minnesota, California, Indiana and Oklahoma", "product_quantity": "7 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0930-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0840-2025", "event_id": "96689", "report_date": "2025-06-11", "recall_initiation_date": "2025-05-02", "center_classification_date": "2025-06-03", "termination_date": "2026-03-18", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Nordic Naturals, Inc.", "city": "Watsonville", "state": "CA", "country": "United States", "product_description": "Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case", "product_short": "Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies", "reason_for_recall": "Product is mislabeled.", "code_info": "Lot: 244423 RUS-30127 Expiration 05/2026", "distribution_pattern": "Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE", "product_quantity": "1164 bottles (120 gummies/bottle)", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0840-2025%22", "category": "labeling", "ingredientSlugs": [ "multivitamins" ], "slug": null }, { "recall_number": "F-0807-2025", "event_id": "96749", "report_date": "2025-05-28", "recall_initiation_date": "2025-04-25", "center_classification_date": "2025-05-20", "termination_date": "2025-07-08", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "My Life Inc", "city": "Federal Way", "state": "WA", "country": "United States", "product_description": "Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.", "product_short": "Lactoferrin as Apolactoferrin", "reason_for_recall": "Undeclared milk allergen", "code_info": "Lot #FL2407511L19 Batch #FL2407511 Expire By/Expiration date 10/2027 Batch #FL2407511 is the CoA Batch Number from supplier and L19 is the recalling firm's internal code for Lactoferrin.", "distribution_pattern": "Sold to online consumers nationwide and distributed to Korea.", "product_quantity": "65 bottles in US and 62 bottles in South Korea", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0807-2025%22", "category": "allergen", "ingredientSlugs": [ "lactoferrin" ], "slug": "2025-05-my-life" }, { "recall_number": "F-0756-2025", "event_id": "96713", "report_date": "2025-05-14", "recall_initiation_date": "2025-04-15", "center_classification_date": "2025-05-05", "termination_date": "2025-09-09", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Optimal Carnivore, LLC", "city": "Cheyenne", "state": "WY", "country": "United States", "product_description": "Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carnivore LLC 1603 Capitol Ave Ste 310 WY371 Cheyenne, WY 82001", "product_short": "Bone & Joint Restore", "reason_for_recall": "Potential for contamination with salmonella.", "code_info": "Expiration date 12/2026. Lot # 1224064", "distribution_pattern": "Nationwide.", "product_quantity": "1483 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0756-2025%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0729-2025", "event_id": "96657", "report_date": "2025-04-30", "recall_initiation_date": "2025-04-04", "center_classification_date": "2025-04-22", "termination_date": "2025-09-03", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Supplement Manufacturing Partner Inc.", "city": "Largo", "state": "FL", "country": "United States", "product_description": "Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellulose, Rice Flour", "product_short": "Spermidine", "reason_for_recall": "Undeclared allergen: Wheat", "code_info": "Lot 12792402-44", "distribution_pattern": "Product was distributed throughout the United States and Germany.", "product_quantity": "6,465 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0729-2025%22", "category": "allergen", "ingredientSlugs": [ "spermidine" ], "slug": "2025-04-supplement-manufacturing-partner" }, { "recall_number": "F-0698-2025", "event_id": "96578", "report_date": "2025-04-16", "recall_initiation_date": "2025-03-25", "center_classification_date": "2025-04-09", "termination_date": "2025-05-28", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "MTN OPS, LLC", "city": "Fruit Heights", "state": "UT", "country": "United States", "product_description": "MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively for MTN OPS, LLC, 251 S Mountain Rd., Fruit Heights, UT. UPC 8 40359 40458 2", "product_short": "MTN OPS MULTI-V Men's Daily Multivitamin", "reason_for_recall": "Undeclared soy flour", "code_info": "Expiration Date: 03/2026, Lot# 012324177", "distribution_pattern": "Distributed nationwide except RI and distributed in Canada", "product_quantity": "7546 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0698-2025%22", "category": "allergen", "ingredientSlugs": [ "multivitamins" ], "slug": null }, { "recall_number": "F-0709-2025", "event_id": "96562", "report_date": "2025-04-09", "recall_initiation_date": "2025-03-21", "center_classification_date": "2025-04-14", "termination_date": "2025-09-03", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Bioriginal Food & Science Corporation", "city": "Saskatoon", "state": "", "country": "Canada", "product_description": "Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with cap, Manufactured for Natural Slim, San Juan Puerto Rico", "product_short": "Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil", "reason_for_recall": "Undeclared allergens: Soy lecithin", "code_info": "Lot Code: PRP403337", "distribution_pattern": "Puerto Rico", "product_quantity": "61 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0709-2025%22", "category": "allergen", "ingredientSlugs": [ "flaxseed-oil", "omega-3" ], "slug": null }, { "recall_number": "F-0671-2025", "event_id": "96473", "report_date": "2025-04-02", "recall_initiation_date": "2025-03-10", "center_classification_date": "2025-03-27", "termination_date": "2025-04-04", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Veridance Pharmacal, LLC", "city": "Springdale", "state": "AR", "country": "United States", "product_description": "Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distributed by: McDonagh Medical Center Gladstone, MO 64119", "product_short": "Omni-Macs McDonagh Medical Center", "reason_for_recall": "Levels of iodine exceeding label claim", "code_info": "UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26", "distribution_pattern": "One customer located in Gladstone, MO", "product_quantity": "450 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0671-2025%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0468-2025", "event_id": "95959", "report_date": "2025-02-12", "recall_initiation_date": "2024-12-11", "center_classification_date": "2025-02-03", "termination_date": "2026-09-11", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vidaslim Co.", "city": "San Antonio", "state": "TX", "country": "United States", "product_description": "VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and Root Capsules), and VidaSlim Hot Body Brew (Strawberry and Peach flavors),", "product_short": "VidaSlim 90-day", "reason_for_recall": "Due to the presence of Toxic yellow oleander", "code_info": "Expiration date of 12/24 (December 2024) through 12/25 (December 2025)", "distribution_pattern": "These products were sold on a website and through direct sales via independent distributors throughout the USA.", "product_quantity": "760 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0468-2025%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0455-2025", "event_id": "96054", "report_date": "2025-02-05", "recall_initiation_date": "2024-12-18", "center_classification_date": "2025-01-29", "termination_date": "2025-11-03", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Iovate Health Sciences USA Inc.", "city": "Wilmington", "state": "DE", "country": "United States", "product_description": "Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in a cool, dry place (60 F to 80 F), UPC 6-31656-60676-8, SKU0001191, SKU0002075", "product_short": "Alpha Test", "reason_for_recall": "Presence of cathine in product", "code_info": "Expiration Date and Lot Codes: March 21, 2027 (Lots 24A125, 24B059, 24B060) March 22, 2027 (Lot 24C112) July 3, 2027 (Lots 24F164, 24G112) July 4, 2027 (Lot 24E288) July 5, 2027 (Lots 24G243, 24H207)", "distribution_pattern": "Domestic and foreign distribution:NC, CA, TX, NJ, VA, NV, PA, IN, NY, CA, IL,MS, KY, MI,SC, WA, CT, FL, OH, WI, DE, LA, TN, MO, UT, KH, GA, KS, CO, IA, AZ, OR. Foreign distribution: ZA, PH, IS, KZ, AE", "product_quantity": "Total 163,248 units", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0455-2025%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0401-2025", "event_id": "96000", "report_date": "2025-01-22", "recall_initiation_date": "2022-08-03", "center_classification_date": "2025-01-15", "termination_date": "2025-01-15", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Eclectic Institute Inc", "city": "Gresham", "state": "OR", "country": "United States", "product_description": "Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham, OR 97030. The affected label declared \"Oregon Grape 190mg ***Oregon Grape 97mg***Cayenne Root (Allium sativum) 195mg ***Ginger Fruit (Capsicum annuum) 65mg***\".", "product_short": "Eclectic Herb Vitamin Herb Blend vita biotic", "reason_for_recall": "Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel.", "code_info": "Lot 25183; Exp date 10/2024 Lot 25543; Exp Date 03/2025", "distribution_pattern": "nationwide", "product_quantity": "1334 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0401-2025%22", "category": "other", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0316-2025", "event_id": "95916", "report_date": "2025-01-01", "recall_initiation_date": "2024-12-04", "center_classification_date": "2024-12-24", "termination_date": "2025-03-03", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Zoe US, Inc.", "city": "Canton", "state": "MA", "country": "United States", "product_description": "ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch", "product_short": "ZOE Daily 30+ Prebiotic blend", "reason_for_recall": "Product may contain foreign objects: small metal pieces and/or stones", "code_info": "Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288", "distribution_pattern": "Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Illinois, Kentucky, Maine, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin", "product_quantity": "142 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0316-2025%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0262-2025", "event_id": "95737", "report_date": "2024-12-18", "recall_initiation_date": "2024-10-30", "center_classification_date": "2024-12-09", "termination_date": "2025-09-24", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Deseret Biologicals Inc", "city": "Sandy", "state": "UT", "country": "United States", "product_description": "DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.", "product_short": "DesBio lunaSOMM Natural Sleep Support", "reason_for_recall": "Product contains undeclared soy lecithin.", "code_info": "LOT 020323126 MFG 04/2023", "distribution_pattern": "Distributed nationwide, one foreign distributor to Australia. No DOD distribution. No VA.", "product_quantity": "2547 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0262-2025%22", "category": "allergen", "ingredientSlugs": [ "phosphatidylserine" ], "slug": null }, { "recall_number": "F-0139-2025", "event_id": "95519", "report_date": "2024-11-27", "recall_initiation_date": "2024-10-07", "center_classification_date": "2024-11-17", "termination_date": "2026-06-24", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Nestle Product Technology Center - Nestle Health Science", "city": "Bridgewater", "state": "NJ", "country": "United States", "product_description": "Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026", "product_short": "Douglas Labs Stress-B-Plus", "reason_for_recall": "Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot Numbers 50335944,50344396, expiration date 04/11/2026. The product is being recalled because of Incorrect formulation manufactured vs label claims. Product was manufactured with Niacin (as Nicotinic acid) and supplement facts panel states contains Niacin (as Niacinamide).", "code_info": "Lot Codes: 50335944, 50344396", "distribution_pattern": "AK,AZ,CA,CO,DE,FL,GA,IA,ID,IL,IN,KS,KY,LA,MA,MD,MI,MN,MO,NC,NH,NJ,NM,NY,OH,OK,OR,PA,SD,TN,TX,VA,WA,WI,WV", "product_quantity": "3,269 bottles in market", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0139-2025%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0053-2025", "event_id": "95313", "report_date": "2024-10-23", "recall_initiation_date": "2024-09-06", "center_classification_date": "2024-10-17", "termination_date": "2025-03-15", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Gorilla Mind LLC", "city": "Boise", "state": "ID", "country": "United States", "product_description": "Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased Energy, dosage 3mg, 90 capsules per bottle, UPC 8 50017 02016 0. Product is manufactured for Gorilla Mind LLC 7154 W. State Street, STE 138, Boise, ID. Product label declares \"***Supplement Facts: Rauwolscine Extract***Other Ingredients: Rice Flour, Gelatin (capsule), Silicon Dioxide, and Magnesium Stearate***\".", "product_short": "Gorilla Mind Rauwolscine", "reason_for_recall": "Product was recalled due to the potential for contamination with Salmonella", "code_info": "Lot Number: 24041003 EXP: 04/2026", "distribution_pattern": "nationwide", "product_quantity": "1348 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0053-2025%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1459-2024", "event_id": "94577", "report_date": "2024-07-10", "recall_initiation_date": "2024-05-03", "center_classification_date": "2024-07-02", "termination_date": "2024-07-05", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Grato Holdings, Inc.", "city": "Woodbine", "state": "IA", "country": "United States", "product_description": "BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml) bottle.", "product_short": "BioActive Nutritional MINAPLEX", "reason_for_recall": "Potential microbial contamination (yeast and/or mold).", "code_info": "Lot J28761", "distribution_pattern": "Nationwide US and Canada", "product_quantity": "261 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1459-2024%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1458-2024", "event_id": "94577", "report_date": "2024-07-10", "recall_initiation_date": "2024-05-03", "center_classification_date": "2024-07-02", "termination_date": "2024-07-05", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Grato Holdings, Inc.", "city": "Woodbine", "state": "IA", "country": "United States", "product_description": "Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle.", "product_short": "Energique Mineral Magic", "reason_for_recall": "Potential microbial contamination (yeast and/or mold).", "code_info": "Lot: G11602 MFD: 06/21; Lot G11747 MFD: 07/22; Lot: G11723 MFD 08/22", "distribution_pattern": "Nationwide US and Canada", "product_quantity": "1912 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1458-2024%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1432-2024", "event_id": "94762", "report_date": "2024-07-10", "recall_initiation_date": "2024-06-03", "center_classification_date": "2024-06-28", "termination_date": "2025-02-19", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Penn Herb Company, Ltd.", "city": "Philadelphia", "state": "PA", "country": "United States", "product_description": "Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closure", "product_short": "Nature's Wonderland Thyroid Formula", "reason_for_recall": "Potential Salmonella contamination", "code_info": "Item #:Sm32x Batch Lot #:23289A", "distribution_pattern": "Distributed to customers in PA, CA, IL, FL, MI, MD, MO, OH, and NY.", "product_quantity": "51 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1432-2024%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1391-2024", "event_id": "94346", "report_date": "2024-07-03", "recall_initiation_date": "2024-04-03", "center_classification_date": "2024-06-21", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "World Green Nutrition Inc.", "city": "San Antonio", "state": "TX", "country": "United States", "product_description": "ELV Control Herbal Supplement; 90 Capsules", "product_short": "ELV Control", "reason_for_recall": "FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.", "code_info": "N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928; 190620231573678B 062828280620231; 573678BA 062828", "distribution_pattern": "Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.", "product_quantity": "20,092 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1391-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1237-2024", "event_id": "94438", "report_date": "2024-05-22", "recall_initiation_date": "2024-03-12", "center_classification_date": "2024-05-10", "termination_date": "2024-06-20", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "East West Tea Company, LLC", "city": "Eugene", "state": "OR", "country": "United States", "product_description": "Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 tea bag, 16 tea bags per pack, 4 packs per box. UPC on box: 0 76950 45010 3. CASE GTIN: 60076950450105. East West Tea Company, LLC Eugene, OR Yogi Echinacea Immune Support, Caffeine Herbal Supplement, 16 tea bags per pack, 6 Packs per box. UPC on box: 0 76950 45010 3. CASE GTIN: 20076950450107.", "product_short": "Organic Yogi Echinacea Immune Support", "reason_for_recall": "Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.", "code_info": "Lot #0000184330 Lot #0000184853 Lot #0000185098 Lot #0000185100 Lot #0000185383 Lot #0000185385 Lot #0000185387 Lot #0000185389 Lot #0000185434 Lot #0000185436 Lot #0000185828 Lot #0000185830 Lot #0000185832 Lot #0000186519 Lot #0000186521 Lot #000184062 Lot #0000186900 Lot #0000186902 Lot #0000186904 Lot #0000187357 Lot #0000187359 Lot #0000187400 Lot #0000187402 Lot #0000187769 Lot #0000188028 Lot #0000188030 Lot #0000188045 Lot #0000188114 Lot #0000186600 Lot #0000186910 Lot #0000187155 Lot #0000184691 Lot #0000184963 Lot #0000185381 Lot #0000185518", "distribution_pattern": "nationwide", "product_quantity": "total 54846 packs", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1237-2024%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1222-2024", "event_id": "94230", "report_date": "2024-05-15", "recall_initiation_date": "2024-03-12", "center_classification_date": "2024-05-08", "termination_date": "2024-06-25", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "HTO Nevada Inc DBA Kirkman", "city": "Lake Oswego", "state": "OR", "country": "United States", "product_description": "Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120 capsules per package, UPC 8 12325 02354 7. Manufactured exclusively by: Kirkman, Lake Oswego, OR 9703,", "product_short": "Kirkman 5-MTHF Methyltetrahydrofolate", "reason_for_recall": "Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg).", "code_info": "Lot#: 477-0016, Exp: 08/2025", "distribution_pattern": "Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.", "product_quantity": "366 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1222-2024%22", "category": "labeling", "ingredientSlugs": [ "methylfolate" ], "slug": null }, { "recall_number": "F-1161-2024", "event_id": "93920", "report_date": "2024-04-24", "recall_initiation_date": "2024-02-09", "center_classification_date": "2024-04-16", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "HandNatural", "city": "San Luis", "state": "AZ", "country": "United States", "product_description": "H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.", "product_short": "H&NATURAL TEJOCOTE ROOT", "reason_for_recall": "Product recalled due to the presence of yellow oleander and its components in the product.", "code_info": "No Lot code on label. Expiration date listed as 05/24 and 03/24.", "distribution_pattern": "Firm is 100% internet sales. Distribution is unknown at this time.", "product_quantity": "Unknown at this time.", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1161-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1160-2024", "event_id": "93920", "report_date": "2024-04-24", "recall_initiation_date": "2024-02-09", "center_classification_date": "2024-04-16", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "HandNatural", "city": "San Luis", "state": "AZ", "country": "United States", "product_description": "H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES, 6 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.", "product_short": "H&NATURAL TEJOCOTE ROOT TWO PACK", "reason_for_recall": "Product recalled due to the presence of yellow oleander and its components in the product.", "code_info": "No Lot code on label. Expiration date listed as 05/24 and 03/24.", "distribution_pattern": "Firm is 100% internet sales. Distribution is unknown at this time.", "product_quantity": "Unknown at this time.", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1160-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1158-2024", "event_id": "93920", "report_date": "2024-04-24", "recall_initiation_date": "2024-02-09", "center_classification_date": "2024-04-16", "termination_date": null, "classification": "Class I", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "HandNatural", "city": "San Luis", "state": "AZ", "country": "United States", "product_description": "H&NATURAL TEJOCOTE ROOT Dietary Supplement Net WT 0.36 oz (10g)", "product_short": "H&NATURAL TEJOCOTE ROOT", "reason_for_recall": "Product is being recalled due to the presence of yellow oleander and its components in the product.", "code_info": "No Lot code on label. Expiration date listed as 05/24 & 03/24", "distribution_pattern": "Firm is 100% internet sales. Distribution is unknown at this time.", "product_quantity": "Unknown at this time", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1158-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1125-2024", "event_id": "94226", "report_date": "2024-04-03", "recall_initiation_date": "2024-02-06", "center_classification_date": "2024-04-08", "termination_date": "2024-06-25", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "VRA FORMULATIONS LLC", "city": "Medley", "state": "FL", "country": "United States", "product_description": "TestoFREAK Maximize Testosterone Dietary Supplement 60 capsules per dark amber bottle, 100 bottles per case", "product_short": "TestoFREAK Maximize Testosterone", "reason_for_recall": "Due to sub-potent levels of Zinc", "code_info": "Lot Numbers 21112002 Expiration Date: 12/2024", "distribution_pattern": "Domestic distribution only through internet sales.", "product_quantity": "1569 Bottles", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1125-2024%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1109-2024", "event_id": "93947", "report_date": "2024-04-03", "recall_initiation_date": "2024-02-07", "center_classification_date": "2024-03-28", "termination_date": "2024-06-21", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Nordic Naturals, Inc.", "city": "Watsonville", "state": "CA", "country": "United States", "product_description": "Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle", "product_short": "Nordic Naturals Baby s Vitamin D3 liquid", "reason_for_recall": "Elevated levels of vitamin D3", "code_info": "Lot number 234909", "distribution_pattern": "Products are distributed to 79 consignees, consisting of retailers, distributors, and consumers. Number of consignees who purchased through Amazon are unknown. U.S. distribution to AR, AZ, CA, DC, DE, FL, GA, IA, IL, IN, MA, MD, MI, MN, MO, MS, NC. ND, NH, NJ, NY, OH, OR, PA, RI, TX, VT and WI. Additionally, foreign customers in the Dubai and Kenya.", "product_quantity": "5564 bottles", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1109-2024%22", "category": "labeling", "ingredientSlugs": [ "vitamin-d" ], "slug": null }, { "recall_number": "F-1000-2024", "event_id": "93774", "report_date": "2024-03-06", "recall_initiation_date": "2024-01-06", "center_classification_date": "2024-02-29", "termination_date": "2025-02-14", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "World Green Nutrition Inc.", "city": "San Antonio", "state": "TX", "country": "United States", "product_description": "ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g)", "product_short": "ELV ALIPOTEC MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE", "reason_for_recall": "FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.", "code_info": "LOT Expiration Date 090222 110424 070722 110424 150722N 120724 190722N 120724 150722N-1 120724 110522 120724 070722 120724 040722 120724 260522 120724 190722N-1 120724 150822 120724 160622 92324 030123 030728 150722N 030828 030123 030628 291122 030628 250123 030628 130123 030728 040722 031328 030123 031328 160622 031428 250123 031428 250123 031528 250123 032128 250123 032228 250123 032328 250123 032428 250123 032728 250123 032828 150722N 032828 160622 041928 260123D 041928 190722N 041928 250123 041828 140223 051228 030223 051228 010323 051528 190722N 051528 200722 051228 250123 051228 150722N 051228 020323 052328 260123D 052328 190722N 052428 260123D 071828 010323 071928 030223 071928 260123D 073128 260123D 080228 140223D 081528", "distribution_pattern": "TX, CA, AZ, NC, GA, OR, WA, NM", "product_quantity": "113,500", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1000-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0930-2024", "event_id": "93899", "report_date": "2024-03-06", "recall_initiation_date": "2024-01-25", "center_classification_date": "2024-02-26", "termination_date": "2024-02-29", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Ancient Formulas, Inc.", "city": "Wichita", "state": "KS", "country": "United States", "product_description": "Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.", "product_short": "Healthprint Vitamin D3 5000", "reason_for_recall": "Product is sub-potent for Vitamin D and label contains incorrect percent daily value.", "code_info": "Lot 063-0723", "distribution_pattern": "FL", "product_quantity": "111 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0930-2024%22", "category": "labeling", "ingredientSlugs": [ "vitamin-d" ], "slug": null }, { "recall_number": "F-0907-2024", "event_id": "93916", "report_date": "2024-02-28", "recall_initiation_date": "2024-02-01", "center_classification_date": "2024-02-20", "termination_date": "2025-11-21", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "The Procter & Gamble Company", "city": "Cincinnati", "state": "OH", "country": "United States", "product_description": "Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.", "product_short": "Meta Psyllium Fiber Capsules", "reason_for_recall": "Illegible Label", "code_info": "Lot Codes (100 count): 31661725G1, 32151725G1, 324211725G1, 32481725G1, 32611725G1, 32901725G1, 33131725G1, 33311725G1, 33411725G1, 33451725G1 Product No (100 count): 80374550 Case UPC (100count): 10037000405143 Item UPC (100 count): 037000405146 Expiration Dates (100 count): 05/31/2026, 06/30/2026, 07/31/2026, 08/31/2026, 09/30/2026, 10/31/2026 Lot Codes(160 count): 31651725G2, 32171725G1, 32211725G1, 32411725G1, 32581725G, 32771725G1, 32911725G3, 32961725G1, 33171725G1, 33251725G2, 33451725G2 Product No. (160 count) 80374554 Case UPC (160 count): 10037000405112 Item UPC (16 count): 037000405115 Expiration Dates(for 160 count): 05/30/2026, 06/30/2026, 08/31/2026, 09/30/2026, 10/31/2026", "distribution_pattern": "Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin", "product_quantity": "21,428 cases TOTAL", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0907-2024%22", "category": "labeling", "ingredientSlugs": [ "psyllium" ], "slug": null }, { "recall_number": "F-0710-2024", "event_id": "93627", "report_date": "2024-01-17", "recall_initiation_date": "2023-12-07", "center_classification_date": "2024-01-09", "termination_date": "2024-05-01", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vita 360, LLC", "city": "San Juan", "state": "PR", "country": "United States", "product_description": "Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container description: White Plastic Bottle 300CC with white cap sealed with clear plastic Total Package size: Master Case with 81 Bottles containing 120 capsules each one. Lot no. 2633, Exp. 07/25 Manufactured in the US", "product_short": "SUPREX Plant Based Nutrition Carb & Sugar Block", "reason_for_recall": "FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.", "code_info": "Manufacturer Lot #2633; Expiration Date: 07/25", "distribution_pattern": "Domestic distribution only throughout Puerto Rico", "product_quantity": "1999 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0710-2024%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0664-2024", "event_id": "93512", "report_date": "2024-01-10", "recall_initiation_date": "2023-12-01", "center_classification_date": "2024-01-02", "termination_date": "2024-09-18", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "BioMylz Pvt. Ltd.", "city": "Bengaluru", "state": "N/A", "country": "India", "product_description": "Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton", "product_short": "Spring Valley Biotin & Collagen Liquid", "reason_for_recall": "Potential mold contamination", "code_info": "NSBS2301, NSBS2302, NSBS2303, NSBS2306, NSBS2308", "distribution_pattern": "Distributed to a distribution center in CA and then further distributed to distribution centers and retail stores nationwide.", "product_quantity": "24,324 units", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0664-2024%22", "category": "contamination", "ingredientSlugs": [ "biotin", "collagen" ], "slug": null }, { "recall_number": "F-0505-2024", "event_id": "93371", "report_date": "2023-12-20", "recall_initiation_date": "2023-10-13", "center_classification_date": "2023-12-08", "termination_date": "2024-01-25", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "LGNDS LLC", "city": "Miami", "state": "FL", "country": "United States", "product_description": "TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583622, POWERED BY LGNDS, 12 bottles of 2oz each per case.", "product_short": "TYSON 2.0", "reason_for_recall": "Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.", "code_info": "Lot #U20231558, BEST BY: 21 JUL 24", "distribution_pattern": "U.S. distribution only.", "product_quantity": "15,000 units of 2oz each", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0505-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0504-2024", "event_id": "93371", "report_date": "2023-12-20", "recall_initiation_date": "2023-10-13", "center_classification_date": "2023-12-08", "termination_date": "2024-01-25", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "LGNDS LLC", "city": "Miami", "state": "FL", "country": "United States", "product_description": "TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583608, POWERED BY LGNDS, 12 bottles of 2oz each per case.", "product_short": "TYSON 2.0", "reason_for_recall": "Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.", "code_info": "Lot #U19231550, BEST BY: 11 JUL 24", "distribution_pattern": "U.S. distribution only.", "product_quantity": "15,000 units of 2oz each", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0504-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0484-2024", "event_id": "93289", "report_date": "2023-12-13", "recall_initiation_date": "2023-10-19", "center_classification_date": "2023-12-01", "termination_date": "2024-02-14", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Garden Of Life Llc", "city": "West Palm Beach", "state": "FL", "country": "United States", "product_description": "Garden of Life, RM-10 ULTRA, Ultimate Immune System Support60 Vegetarian Caplets, Whole Food Dietary Supplement, 90 Ultra Zorbe Vegetarian Capsules", "product_short": "Garden of Life", "reason_for_recall": "Undeclared Soy.", "code_info": "Lot Numbers: 50304364, 50298662 Exp. Dates: 2/2024-9/2024", "distribution_pattern": "Domestic and foreign distribution.", "product_quantity": "8,940 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0484-2024%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0483-2024", "event_id": "93289", "report_date": "2023-12-13", "recall_initiation_date": "2023-10-19", "center_classification_date": "2023-12-01", "termination_date": "2024-02-14", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Garden Of Life Llc", "city": "West Palm Beach", "state": "FL", "country": "United States", "product_description": "Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement", "product_short": "Garden of Life", "reason_for_recall": "Undeclared Soy.", "code_info": "Lot Numbers: 50298707, 50315317, 50298646, 50283628 Exp. Dates: 1/2024-8/2024", "distribution_pattern": "Domestic and foreign distribution.", "product_quantity": "15,119 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0483-2024%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0482-2024", "event_id": "93289", "report_date": "2023-12-13", "recall_initiation_date": "2023-10-19", "center_classification_date": "2023-12-01", "termination_date": "2024-02-14", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Garden Of Life Llc", "city": "West Palm Beach", "state": "FL", "country": "United States", "product_description": "Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement, 120 Ultra Zorbe VEGETARIAN CAPSULES", "product_short": "Garden of Life", "reason_for_recall": "Undeclared Soy.", "code_info": "Lot Numbers: 50312871, 50293093, 50278965, 5028258 Exp. Dates: 10/2023-6/2024", "distribution_pattern": "Domestic and foreign distribution.", "product_quantity": "37, 424 bottles", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0482-2024%22", "category": "allergen", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0463-2024", "event_id": "93210", "report_date": "2023-11-29", "recall_initiation_date": "2023-09-28", "center_classification_date": "2023-11-17", "termination_date": "2024-01-16", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "ActiPharma, Inc.", "city": "Guaynabo", "state": "PR", "country": "United States", "product_description": "ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.", "product_short": "ACTIRON", "reason_for_recall": "FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.", "code_info": "Lot 13309, Exp: 01/26", "distribution_pattern": "Domestic distribution, in Puerto Rico.", "product_quantity": "607 bottles of 100 tablets each", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0463-2024%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0320-2024", "event_id": "93157", "report_date": "2023-11-15", "recall_initiation_date": "2023-09-21", "center_classification_date": "2023-11-03", "termination_date": "2024-01-25", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Kula Brands LLC", "city": "Naples", "state": "FL", "country": "United States", "product_description": "Kula Can Pina Colada + KRATOM SELTZER, 12 oz (355ML) DIETARY SUPPLEMENT", "product_short": "Kula Can Pina Colada + KRATOM SELTZER", "reason_for_recall": "Undeclared Allergens: Milk and Tree Nut (Coconut) and Unapproved Food Additive: Kratom", "code_info": "Lot Number U17831532PNCL Exp. Date 7/27/24", "distribution_pattern": "Domestic distribution only.", "product_quantity": "7,062 cans", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0320-2024%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0313-2024", "event_id": "93235", "report_date": "2023-11-08", "recall_initiation_date": "2023-10-13", "center_classification_date": "2023-11-02", "termination_date": "2024-04-12", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Select Custom Solutions, LLC", "city": "La Crosse", "state": "WI", "country": "United States", "product_description": "JayRobb Vanilla Flavored Egg White Protein Powder. Net Weight 24 oz (1.5 lbs) 680g Dietary Supplement. UPC 6 03907-00462 3", "product_short": "JayRobb Vanilla Flavored Egg White Protein Powder", "reason_for_recall": "foreign material - plastic", "code_info": "Lot# 23080-2C2 with time stamps 09:00 - 12:00 Best If Used By: 03/2025", "distribution_pattern": "Nationwide", "product_quantity": "1,008 pouches", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0313-2024%22", "category": "contamination", "ingredientSlugs": [ "protein" ], "slug": null }, { "recall_number": "F-1615-2023", "event_id": "92953", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-15", "center_classification_date": "2023-09-27", "termination_date": "2024-01-19", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Pharma-Natural Inc.", "city": "Miami Lakes", "state": "FL", "country": "United States", "product_description": "Pharma Natural, Biotin 5000 mcg, Maximum Strength, Dietary Supplement, 30 Tablets", "product_short": "Pharma Natural", "reason_for_recall": "FDA sample analysis of Pharma Natural Biotin 5000 mcg Maximum Strength (30 tablets, Lot: PN10686, Exp. Date 01/24), found the biotin content was below the detection limit.", "code_info": "Lot: PN10686, Exp. Date 01/24", "distribution_pattern": "Puerto Rico", "product_quantity": "204 bottles (102 twin packs)/30 tablets per bottle", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1615-2023%22", "category": "other", "ingredientSlugs": [ "biotin" ], "slug": null }, { "recall_number": "F-1600-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1600-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1599-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1599-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1598-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1598-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1597-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1597-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1596-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1593-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1592-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1592-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1591-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1591-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1590-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1590-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1589-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1589-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1588-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1588-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1587-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1587-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1586-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1586-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1585-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1584-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1583-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). 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Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1551-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1550-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1550-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1549-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1549-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1548-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1548-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1547-2023", "event_id": "92936", "report_date": "2023-10-04", "recall_initiation_date": "2023-08-22", "center_classification_date": "2023-09-22", "termination_date": "2023-11-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Vitality Works, Inc", "city": "Albuquerque", "state": "NM", "country": "United States", "product_description": "100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Bottle with White Polypropylene Cap. Product distributed under multiple brands.", "product_short": "100 vegetarian Fenugreek Capsules", "reason_for_recall": "Foreign material: pieces of a pen (writing utensil).", "code_info": "Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28", "distribution_pattern": "55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023", "product_quantity": "1,025 bottles (total)", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1547-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1544-2023", "event_id": "92919", "report_date": "2023-09-27", "recall_initiation_date": "2023-09-05", "center_classification_date": "2023-09-19", "termination_date": "2024-02-07", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "OBC GROUP CORP", "city": "Doral", "state": "FL", "country": "United States", "product_description": "NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps", "product_short": "NUT DIET MAX", "reason_for_recall": "Product appears to be Yellow Oleander instead of Nuez de la India as labeled.", "code_info": "Exp. Date 11/2025", "distribution_pattern": "Domestic distribution only.", "product_quantity": "Unknown", "initial_firm_notification": "Letter", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1544-2023%22", "category": "tainted", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1443-2023", "event_id": "92751", "report_date": "2023-08-23", "recall_initiation_date": "2023-07-13", "center_classification_date": "2023-08-17", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Global Vitality Inc.", "city": "Chandler", "state": "AZ", "country": "United States", "product_description": "Food Research International - Serious Brain Enhancer Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case", "product_short": "Food Research International - Serious Brain Enhancer Capsules", "reason_for_recall": "potential contamination with E coli", "code_info": "Item # B6506 Lot #9231 Product # DRR6506-90VC Best By 10/25", "distribution_pattern": "Distributed to single consignee in California", "product_quantity": "2975 bottles total", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1443-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1442-2023", "event_id": "92751", "report_date": "2023-08-23", "recall_initiation_date": "2023-07-13", "center_classification_date": "2023-08-17", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Global Vitality Inc.", "city": "Chandler", "state": "AZ", "country": "United States", "product_description": "Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case", "product_short": "Food Research International - Uro Kid Support Capsules", "reason_for_recall": "potential contamination with E coli", "code_info": "Item # B6517 Lot #9237 Product # DRR6517-90VC Best By 01/26", "distribution_pattern": "Distributed to single consignee in California", "product_quantity": "2975 bottles total", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1442-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1296-2023", "event_id": "92685", "report_date": "2023-08-02", "recall_initiation_date": "2023-07-10", "center_classification_date": "2023-07-26", "termination_date": "2024-01-10", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Emceta International Inc.", "city": "Doral", "state": "FL", "country": "United States", "product_description": "Natural Systems, HAIR - SKIN NAIL, Dietary Supplement 60 Capsules", "product_short": "Natural Systems", "reason_for_recall": "FDA evaluation of Natural Systems brand HAIR - SKIN NAIL Dietary Supplement label disclosed several deficiencies to 21 CFR 101 Labeling Regulations.", "code_info": "Lot 42049, MFG 04/2022, Exp. 04/2025", "distribution_pattern": "Domestic and Foreign distribution.", "product_quantity": "576 bottles/60 capsules each", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1296-2023%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1295-2023", "event_id": "92685", "report_date": "2023-08-02", "recall_initiation_date": "2023-07-10", "center_classification_date": "2023-07-26", "termination_date": "2024-01-10", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Emceta International Inc.", "city": "Doral", "state": "FL", "country": "United States", "product_description": "Natural Systems, Naturasys MULTI VITAMIN HIGH POTENCY AND FORMULATION, Dietary Supplement 60 Tablets", "product_short": "Natural Systems", "reason_for_recall": "FDA sample analysis of Natural Systems brand Multi Vitamin, 60 Tablets, found the magnesium content as 33.5% of the amount declared in label.", "code_info": "Lot 38883, Exp. 07/2024", "distribution_pattern": "Domestic and Foreign distribution.", "product_quantity": "554 bottles/60 tablets each", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1295-2023%22", "category": "labeling", "ingredientSlugs": [ "multivitamins" ], "slug": null }, { "recall_number": "F-1247-2023", "event_id": "92590", "report_date": "2023-07-19", "recall_initiation_date": "2023-06-21", "center_classification_date": "2023-07-11", "termination_date": "2024-01-25", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "International Food Companies DBA International Food Products", "city": "Hazelwood", "state": "MO", "country": "United States", "product_description": "1st phorm Level-1 Sustained Assimilation Protein. Milk Chocolate. Protein Supplement. Item number 502066. Net Wt. 2.45 lbs (1.11kg) UPC 8 50026-19672 6. Manufactured & Designed Exclusively for 1st Phorm, 2091 Fenton Logistics Pk Blvd, Fenton, MO 63026", "product_short": "1st phorm Level-1 Sustained Assimilation Protein", "reason_for_recall": "Product may contain Staphylococcus aureus.", "code_info": "lot 23088AP8A", "distribution_pattern": "MO", "product_quantity": "480 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1247-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-1246-2023", "event_id": "92590", "report_date": "2023-07-19", "recall_initiation_date": "2023-06-21", "center_classification_date": "2023-07-11", "termination_date": "2024-01-25", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "International Food Companies DBA International Food Products", "city": "Hazelwood", "state": "MO", "country": "United States", "product_description": "1st phorm Level-1 Sustained Assimilation Protein. Chocolate Marshmallow. Protein Supplement. Item number 502396. Net Wt. 2.45 lbs (1.11kg) UPC 8 50036-64808 6. Manufactured & Designed Exclusively for 1st Phorm, 2091 Fenton Logistics Pk Blvd, Fenton, MO 63026", "product_short": "1st phorm Level-1 Sustained Assimilation Protein", "reason_for_recall": "Product may contain Staphylococcus aureus.", "code_info": "Lot 23087AP8A", "distribution_pattern": "MO", "product_quantity": "126 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1246-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0978-2023", "event_id": "92385", "report_date": "2023-06-14", "recall_initiation_date": "2023-05-19", "center_classification_date": "2023-06-07", "termination_date": "2023-11-30", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Procaps S.A. de C.V.", "city": "Soyapango", "state": "", "country": "El Salvador", "product_description": "Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard box", "product_short": "Bacaolinita Liquid", "reason_for_recall": "PEG-40 not declared as an ingredient on the label", "code_info": "Lot #: 1358739, 1379697, 1379718, 1387103, 1404273, 1416127, 1420872, 1423729, 1451962", "distribution_pattern": "DE, TX, CA", "product_quantity": "33,684 Boxes", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0978-2023%22", "category": "labeling", "ingredientSlugs": [ "b12" ], "slug": null }, { "recall_number": "F-0886-2023", "event_id": "92237", "report_date": "2023-05-24", "recall_initiation_date": "2023-04-27", "center_classification_date": "2023-05-12", "termination_date": "2023-12-13", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Big Bold Health Holdings Inc", "city": "Bainbridge Island", "state": "WA", "country": "United States", "product_description": "Microbiome Rejuvenate dietary supplement, 60 capsules per bottle, UPC: 8 50033 36201 5. Distributed by Big Bold Health, Bainbridge Island, WA.", "product_short": "Microbiome Rejuvenate", "reason_for_recall": "Glass fragments.", "code_info": "Lot #10249, EXP: 01/10/2025", "distribution_pattern": "U.S. nationwide including Puerto Rico and to the following foreign countries: Australia, Canada, Sweden, Switzerland, and Taiwan.", "product_quantity": "1,087 bottles", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0886-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0841-2023", "event_id": "92162", "report_date": "2023-05-17", "recall_initiation_date": "2023-04-20", "center_classification_date": "2023-05-10", "termination_date": "2023-09-19", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Euro-Pharma", "city": "Green Bay", "state": "WI", "country": "United States", "product_description": "Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for: Euromedica, 925 Challenger Drive, Green Bay, WI 54311. 2. Terry Naturally BioActive Vitamin B, Product #18006, UPC 3 67703-18006 5. Manufactured by a cGMP compliant facility exclusively for: EuroPharma, Inc., Green Bay, WI 54311.", "product_short": "Multiple Vitamin B Capsules", "reason_for_recall": "undeclared allergen (milk)", "code_info": "1. Active B, Lot # 1220019, Best By Date: November 2022; Lot # 0921232, Best By Date: July 2023; Lot # 0222190, Best By Date: January 2024. 2. BioActiva, Lot # 1220022, Best By Date: October 2022; Lot # 0921231, Best By Date: July 2023; Lot # 0222192, Best By Date: January 2024; Lot # 0223570, Best By Date: December 2024.", "distribution_pattern": "Nationwide", "product_quantity": "23,770 units total", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0841-2023%22", "category": "allergen", "ingredientSlugs": [ "multivitamins", "b12", "methylfolate", "b-complex" ], "slug": null }, { "recall_number": "F-0822-2023", "event_id": "92087", "report_date": "2023-05-17", "recall_initiation_date": "2023-03-29", "center_classification_date": "2023-05-05", "termination_date": null, "classification": "Class II", "status": "Ongoing", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "FLP LLC", "city": "Tempe", "state": "AZ", "country": "United States", "product_description": "Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.", "product_short": "Dr. Rico Perez Super Kids Colostrum", "reason_for_recall": "Colostrum is declared but label does not declare milk.", "code_info": "Lot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025.", "distribution_pattern": "Distributed in CA, FL, NJ, and NY.", "product_quantity": "Lot 1117002 = 5,760 bottles; Lot 0122003 = 1,800 bottles; Lot 0223539 = 180 bottles", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0822-2023%22", "category": "allergen", "ingredientSlugs": [ "colostrum" ], "slug": null }, { "recall_number": "F-0812-2023", "event_id": "92070", "report_date": "2023-05-10", "recall_initiation_date": "2023-03-27", "center_classification_date": "2023-05-04", "termination_date": "2023-08-15", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Novis PR, LLC dba Kramer Novis", "city": "San Juan", "state": "PR", "country": "United States", "product_description": "PreProtein, Liquid Predigested Protein, Dietary Supplement, Nt Wt. 16 oz Bottle, packed in 12 units of 16 oz. each per case.", "product_short": "PreProtein", "reason_for_recall": "Bloated Protein Bottle", "code_info": "lot 230131 UPC Code:52083533167", "distribution_pattern": "Domestic distribution only.", "product_quantity": "513 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0812-2023%22", "category": "other", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0811-2023", "event_id": "92070", "report_date": "2023-05-10", "recall_initiation_date": "2023-03-27", "center_classification_date": "2023-05-04", "termination_date": "2023-08-15", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Novis PR, LLC dba Kramer Novis", "city": "San Juan", "state": "PR", "country": "United States", "product_description": "PreProtein, Liquid Predigested Protein, Dietary Supplement, Nt Wt. 30 mL pouch, packed 200 units of 30mL in 1 case", "product_short": "PreProtein", "reason_for_recall": "Bloated Protein Bottle", "code_info": "lot 230118 UPC Code:52083533105", "distribution_pattern": "Domestic distribution only.", "product_quantity": "4106 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0811-2023%22", "category": "other", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0810-2023", "event_id": "92070", "report_date": "2023-05-10", "recall_initiation_date": "2023-03-27", "center_classification_date": "2023-05-04", "termination_date": "2023-08-15", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Novis PR, LLC dba Kramer Novis", "city": "San Juan", "state": "PR", "country": "United States", "product_description": "GPre Protein, Liquid predigested Protein, Dietary Supplement, Nt Wt. 16 oz, plastic bottle packed 12 units of 16 oz in 1 case.", "product_short": "GPre Protein", "reason_for_recall": "Bloated Protein Bottle", "code_info": "lot 230118 UPC Code: 52083633164", "distribution_pattern": "Domestic distribution only.", "product_quantity": "6,034 units", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0810-2023%22", "category": "other", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0733-2023", "event_id": "91571", "report_date": "2023-04-26", "recall_initiation_date": "2023-03-07", "center_classification_date": "2023-04-14", "termination_date": "2023-08-18", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Natural Solutions Foundation", "city": "Newton", "state": "NJ", "country": "United States", "product_description": "Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)", "product_short": "Dr. Rima Recommends The Silver Solution Immune System Support", "reason_for_recall": "Product labeled and intended to mitigate, prevent, or treat COVID-19", "code_info": "unknown", "distribution_pattern": "Distributed to consumers nationwide.", "product_quantity": "Unknown", "initial_firm_notification": "Press Release", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0733-2023%22", "category": "labeling", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0425-2023", "event_id": "91155", "report_date": "2023-03-22", "recall_initiation_date": "2022-11-14", "center_classification_date": "2023-03-10", "termination_date": "2023-11-30", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Mason Vitamins, Inc.", "city": "Miami Lakes", "state": "FL", "country": "United States", "product_description": "Healthy Sense Daily Multiple with Iron, Dietary Supplement, 20 Tablets", "product_short": "Healthy Sense Daily Multiple with Iron", "reason_for_recall": "Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.", "code_info": "Lot No./Expiration Date: - 25807G/9-24 and 25222G/7-24", "distribution_pattern": "Domestic distribution only.", "product_quantity": "37,330 bottles/ 20 tablets ea", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0425-2023%22", "category": "labeling", "ingredientSlugs": [ "iron" ], "slug": null }, { "recall_number": "F-0424-2023", "event_id": "91155", "report_date": "2023-03-22", "recall_initiation_date": "2022-11-14", "center_classification_date": "2023-03-10", "termination_date": "2023-11-30", "classification": "Class III", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Mason Vitamins, Inc.", "city": "Miami Lakes", "state": "FL", "country": "United States", "product_description": "People's Choice Women's Daily Vitamins with Iron, 30 Tablets, Dietary Supplement", "product_short": "People's Choice Women's Daily Vitamins with Iron", "reason_for_recall": "Product is sub-potent for Vitamins A, B12, B5 (Pantothenic acid), C, and E not meeting label claims.", "code_info": "Lot No./Expiration Date o 25807G/9-24 o A25807G/9-24 o B25807G/9-24 o C25807G/9-24 o D25807G/9-24", "distribution_pattern": "Domestic distribution only.", "product_quantity": "224,279 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0424-2023%22", "category": "labeling", "ingredientSlugs": [ "iron" ], "slug": null }, { "recall_number": "F-0340-2023", "event_id": "91515", "report_date": "2023-02-15", "recall_initiation_date": "2023-01-12", "center_classification_date": "2023-02-03", "termination_date": "2024-04-09", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Ortho Molecular Products, Inc.", "city": "Stevens Point", "state": "WI", "country": "United States", "product_description": "Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, packaged under the following brands and sizes. 1.\tOrtho Molecular Products Fiber Plus, Product #608445, Net Wt. 15.9 oz (450 Grams) UPC 6 15033-00608 2. Ortho Molecular Products, Inc., 3017 Business Park Drive, Stevens Point, WI 54482. 2.\tUtzy Naturals, Daily Fiber Drink Mix. Net Wt 5.95 oz (168.75 Grams), UPC 8 56420-00632 6. Manufactured for Utzy Naturals, 623 West Main St., Lake Geneva, WI 53147. 3.\tOrtho Molecular Products Fiber Plus, Product #608445CAN, 450 g, UPC 6 15033-04608 8. Ortho Molecular Products, Inc. 54482 United States. Product is sold in Canada. 4.\tOrtho Molecular Products Fiber Plus, Product #608445C, Net Wt. 15.9 oz (450 Grams) UPC 6 15033-01608 1. . Ortho Molecular Products, Inc., 3017 Business Park Drive, Stevens Point, WI 54482. Contains CA Prop 65. 5.\tUnbranded bottled product in 1000cc bottle to be given out by healthcare provider. 608.008J UPC 6 15033 60608 4. 6.\tUnbranded bottled product in 1000cc bottle to be given out by healthcare provider. 608C.009H UPC 6 15033 61608 3. Contains CA Prop 65.", "product_short": "Fiber Powder", "reason_for_recall": "Raw material tested positive for Cronobacter sakazakii.", "code_info": "Lot 87121 Product Number 608445, 608445C, 608445CAN, and 608445U UPC 615033006082, 615033016081, 615033046088, and 615033606084 Expiration Date 06/30/23 Lot 87059 Product Number 608445, 608445C, 608445CAN, UTZ100-1300168, 608445U UPC 615033006082, 615033016081, 615033046088, 615033606084, and 856420006326 Expiration Date 06/30/23", "distribution_pattern": "Nationwide. Outside the US to Canada.", "product_quantity": "4,929 bottles", "initial_firm_notification": "Telephone", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0340-2023%22", "category": "contamination", "ingredientSlugs": [], "slug": null }, { "recall_number": "F-0323-2023", "event_id": "91377", "report_date": "2023-02-08", "recall_initiation_date": "2021-12-20", "center_classification_date": "2023-01-30", "termination_date": "2023-04-03", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Professional Complementary Health Formulas, LLC", "city": "Lake Oswego", "state": "OR", "country": "United States", "product_description": "Vitamin B Complex packaged in white plastic bottle labeled in part, \"***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin) 80 mg 6154% Vitamin B3 (as niacinamide) 80 mg NE 500% Vitamin B6 (as pyridoxine HCl) 80 mg 4706% Folic acid 667 mcg DFE 167% Vitamin B12 (as cyanocobalamin) 80 mcg 3333% Biotin 300 mcg 1000% Vitamin B5 (as calcium pantothenate) 80 mg 1600% Choline (as bitartrate) 80 mg 15%***Professional Formulas PO Box 2034, Lake Oswego, OR 97035 Recommended Dosage: As a nutritional supplement, take one capsule, or as directed by your healthcare professional***FOR PROFESSIONAL USE ONLY\"", "product_short": "Vitamin B Complex", "reason_for_recall": "Product recalled due to undeclared niacin.", "code_info": "Lot 1092715", "distribution_pattern": "Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.", "product_quantity": "299 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0323-2023%22", "category": "labeling", "ingredientSlugs": [ "b-complex", "vitamin-b6", "methylfolate", "b12", "biotin", "calcium", "choline" ], "slug": null }, { "recall_number": "F-0322-2023", "event_id": "91377", "report_date": "2023-02-08", "recall_initiation_date": "2021-12-20", "center_classification_date": "2023-01-30", "termination_date": "2023-04-03", "classification": "Class II", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "Professional Complementary Health Formulas, LLC", "city": "Lake Oswego", "state": "OR", "country": "United States", "product_description": "Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, \"***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules***Supplement Facts Serving Size: One Capsule***Inositol 920 mg***Other Ingredients: Vegetarian capsule (hypromellose and water) and vegetable stearate Professional Formulas PO Box 2034, Lake Oswego, OR 97035 Recommended Dosage: As a nutritional supplement, take one capsule up to 3 times daily, or as directed by your healthcare professional***FOR PROFESSIONAL USE ONLY\"", "product_short": "Inositol", "reason_for_recall": "Product recalled due to undeclared niacin.", "code_info": "Lot 1032526", "distribution_pattern": "Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.", "product_quantity": "40 bottles", "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0322-2023%22", "category": "labeling", "ingredientSlugs": [ "myo-inositol" ], "slug": null }, { "recall_number": "F-0216-2023", "event_id": "91289", "report_date": "2023-01-11", "recall_initiation_date": "2022-12-05", "center_classification_date": "2023-01-05", "termination_date": "2023-01-10", "classification": "Class I", "status": "Terminated", "voluntary_mandated": "Voluntary: Firm initiated", "recalling_firm": "THGH Partners, LLC", "city": "Calabasas", "state": "CA", "country": "United States", "product_description": "Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protein Mix (pumpkin, sunflower, flax)(as ProteoSMART), Mung Bean Protein, myHMB (Calcium Beta-hydroxy-Beta-Methlbutyrate), Alkalized Cocoa Powder, Pea Protein Powder, Gum Blend (guar gum, xanthan gum), Pink Himalayan Sea Salt, Natural Flavor, Chlorella protothecoides (as AlgaRich vegi-PSS), Digestive Enzyme Blend (Bacillus subtilis, Ananas comosus)(as ProHydrolase). Monk Fruit Extract, Vitamin D3 (plant source) (as VegD3), Chromium Picolinate (as Chromax) Contains Gluten (from Wheat) and Soy (soy and wheat are used in the microbial fermentation of the ProHydrolase enzyme BUT not added into the product). Distributed by Power Life Nutrition 4500 Park Granada Boulevard, Suite 200 Calabasas, CA 91302 855-462-2496 MyPowerLife.com UPC 8 50010 86301 6", "product_short": "Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor", "reason_for_recall": "Incorrect product label causing undeclared milk.", "code_info": "lot 0914922", "distribution_pattern": "Product was sold online only in the United States, United Kingdom, Australia, New Zealand, Canada, and Mexico.", "product_quantity": "6,782 units", "initial_firm_notification": "E-Mail", "openfda_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0216-2023%22", "category": "allergen", "ingredientSlugs": [ "protein", "calcium", "digestive-enzymes", "vitamin-d", "chromium" ], "slug": null } ] }