TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules recall (June 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
Total Nutrition Inc (Deer Park, NY) recalled TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules in a recall FDA classified as Class I. FDA’s stated reason: “Product may be contaminated with Salmonella.”. Started May 22, 2026; posted in the enforcement report June 17, 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: “Nationwide”. Quantity: 13,000 bottles. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 99072, 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 | Total Nutrition Inc, Deer Park, NY |
|---|---|
| Product | 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) |
| Reason for recall (FDA’s text) | “Product may be contaminated with Salmonella.” |
| Classification | Class I |
| Status | Ongoing |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2026-05-22 |
| Enforcement report date | 2026-06-17 |
| FDA classified on | 2026-06-10 |
| Distribution | Nationwide |
| Quantity | 13,000 bottles |
| How the firm notified | |
| Recall number | H-0942-2026 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
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
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 “Total Nutrition Inc” 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 TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules recalled?
FDA's enforcement report gives the reason as: "Product may be contaminated with Salmonella.". FDA records the recall type as "Voluntary: Firm initiated"; Total Nutrition Inc of Deer Park, NY started it May 22, 2026 and it was posted in FDA's enforcement report on June 17, 2026 as Class I.
Which lots of TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules are affected?
FDA's record lists: 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. 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 TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules sold?
FDA's record gives the distribution as: "Nationwide". Quantity recalled: 13,000 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 99072, recall number H-0942-2026. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-0942-2026
- 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.