Lower riskFood recall · FDA · Published May 22, 2026
Total Nutrition Moringa Capsules Recall: Salmonella Contamination Risk
Total Nutrition Inc recalls two types of Moringa capsules due to potential Salmonella contamination. Consumers should check product lots and contact the company for instructions.
“Total Nutrition Moringa Capsules Recall: Salmonella Contamination Risk.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6204-total-nutrition-moringa-capsules-recall-salmonella-contamination-risk. Based on FDA recall #H-0942-2026.
Total Nutrition Inc voluntarily recalled two green superfood moringa capsule products due to potential Salmonella contamination, the FDA announced on May 22, 2026. Approximately 13,000 bottles were distributed nationwide.
2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules), Lot: 2507199 Exp. 09/2027
2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules), Lot: 2748 Exp. 07/2027, UPC: 095234698734; SKU: AB9873
The hazard
The products may be contaminated with Salmonella.
Context
GovInfoNow's records show Total Nutrition Inc has one other recall on record since June 26, 2026. Other recent recalls of similar products include MOGO Moringa Capsules Recall (May 24, 2026), Rosabella Moringa Capsules Recall (Feb. 13, 2026), and Why Not Natural Moringa Capsules Recall (Jan. 28, 2026).
How to tell if you have this one
Check the product lot numbers: 2507199 (exp. 09/2027), 2512-304 (exp. 02/2028), 2793 (exp. 02/2028), or 2748 (exp. 07/2027). The products are sold under ASINs B0DBRDPBDT and SKUs AB8047 or AB9873.
Brand
Total Nutrition Inc
Product
1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Lot Numbers
Look for lot numbers 2507199, 2512-304, 2793, or 2748 on the capsules.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 26 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0942-2026 (May 22, 2026)
Plain-language summary written by qwen3:4b on August 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.