MOGO PURE MORINGA OLEIFERA CAPSULES recall (July 2026): reason, lots, what to do
Not medical advice. This page reproduces one FDA enforcement report and explains its fields; FDA’s text is quoted as FDA’s. If you have this product and any symptoms, your pharmacist or doctor comes before this page.
What was recalled
MOGO Moringa LLC (Saint Louis, MO) recalled MOGO PURE MORINGA OLEIFERA CAPSULES in a recall FDA classified as Class I. FDA’s stated reason: “Product may be contaminated with Salmonella Typhimurium”. Started May 24, 2026; posted in the enforcement report July 8, 2026; status Ongoing.
Class I means, in FDA’s words, a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Distribution: “Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)”. Quantity: 23,186 bottles. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 99071, retrieved from openFDA on September 21, 2026; the last row links to the live record so you can confirm it has not changed.
| Recalling firm | MOGO Moringa LLC, Saint Louis, MO |
|---|---|
| Product | 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 |
| Reason for recall (FDA’s text) | “Product may be contaminated with Salmonella Typhimurium” |
| Classification | Class I |
| Status | Ongoing |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2026-05-24 |
| Enforcement report date | 2026-07-08 |
| FDA classified on | 2026-06-29 |
| Distribution | Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com) |
| Quantity | 23,186 bottles |
| How the firm notified | |
| Recall number | H-1128-2026 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
Find the lot number on the bottom of the container, beside the seal or on the box flap; the expiration date is usually printed next to it. If the code on your container appears above, it is in scope. If the product name matches but the code does not, your unit is not part of this recall, though a second lot is sometimes added later, so re-check the recall list before finishing the bottle.
Why this is a Class I recall
FDA assigns the class by the probability and severity of harm, not by how much product is involved. For this event the reason falls into what we file as contamination (microbial, heavy metal, foreign matter): the product, or a raw material in it, may carry a pathogen, a foreign material or a chemical contaminant. The product itself may be exactly what the label says; the problem is what came with it.
FDA’s definition of Class I (21 CFR 7.3) is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. A Class I recall is the strongest signal FDA sends about a consumer product short of a seizure; it is reserved for the cases where continuing to use the product is itself the risk. The reason text is the authority for this specific event; the class is FDA’s summary judgement of it.
If you bought it
- Stop taking it now; for a Class I recall this is the point of the notice.
- Match your lot against the codes above. Keep the container: the firm’s notice normally offers a refund on proof of the lot number or a photo.
- If you have had symptoms consistent with the contaminant FDA names, tell your doctor and mention the product by name. Then report to FDA MedWatch (online form or 1-800-FDA-1088).
- Check the firm’s other products. A recall event often expands to the same firm’s other SKUs a week or two later. Search “MOGO Moringa LLC” on the full recall list.
Choosing a replacement that can be checked
This product does not name an ingredient we track, so there is no like-for-like guide to send you to. The general rule holds: the only supplements whose contents a buyer can verify are those in a certifier’s public registry (NSF/ANSI 173, NSF Certified for Sport, USP Verified, Informed Sport) or with a lot-specific certificate of analysis the brand publishes. Our registry audit shows how few products clear that bar, and the per-ingredient third-party-tested pages (magnesium, creatine, vitamin D, omega-3, multivitamins) list the ones that do.
Frequently asked questions
Why was MOGO PURE MORINGA OLEIFERA CAPSULES recalled?
FDA's enforcement report gives the reason as: "Product may be contaminated with Salmonella Typhimurium". FDA records the recall type as "Voluntary: Firm initiated"; MOGO Moringa LLC of Saint Louis, MO started it May 24, 2026 and it was posted in FDA's enforcement report on July 8, 2026 as Class I.
Which lots of MOGO PURE MORINGA OLEIFERA CAPSULES are affected?
FDA's record lists: Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028. Match these against the lot number, UPC or expiration date printed on your container; a bottle whose code is not listed is not part of this recall.
Where was MOGO PURE MORINGA OLEIFERA CAPSULES sold?
FDA's record gives the distribution as: "Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)". Quantity recalled: 23,186 bottles.
Is this recall over?
FDA lists the status as "Ongoing". Ongoing means the firm is still retrieving product from the market.
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Sources
- U.S. Food and Drug Administration. Enforcement report, event 99071, recall number H-1128-2026. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-1128-2026
- 21 CFR 7.3(m): recall classification definitions. eCFR Title 21 Part 7.
- FDA. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. fda.gov/safety/medwatch.