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Stop using now Food recall · FDA · Published June 26, 2026

Total Nutrition Moringa Products Recalled Due to Salmonella Contamination

Total Nutrition Inc recalls two products for Salmonella contamination. Consumers should stop using these items immediately to avoid foodborne illness risks.

🇺🇸 FDA recall #H-1185-2026FoodTotal Nutrition ›
✎ GovInfoNow plain-language explainer

Total Nutrition Inc has recalled two products: 1,200 mg Moringa Capsules and 96g Moringa Powder. These items were contaminated with Salmonella, a bacteria that can cause serious food poisoning if ingested. Read more at govinfonow.com/recall/83476-total-nutrition-moringa-products-recalled-due-to-salmonella-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/83476-total-nutrition-moringa-products-recalled-due-to-salmonella-contamination · Updated August 18, 2026 · Official notice: FDA #H-1185-2026

Cite this page

“Total Nutrition Moringa Products Recalled Due to Salmonella Contamination.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/83476-total-nutrition-moringa-products-recalled-due-to-salmonella-contamination. Based on FDA recall #H-1185-2026.

The FDA announced on June 26, 2026, that Total Nutrition Inc is recalling 1. TNVitamins 100% Organic Moringa Capsules and 1. TNVitamins 100% Organic Moringa Powder due to Salmonella contamination. The agency classified the recall as Class I.

How to tell if you have it

  • Brand: Total Nutrition
  • Product: 1. TNVitamins 100% Organic Moringa Capsules 1,200 mg, Product# AB9917, Lot #: 2800, Exp: 2/2028
  • Product: 1. TNVitamins 100% Organic Moringa Powder 96 grams, Product# AB9904, Lot #: 2782, Exp: 5/2028
  • Distribution: nationwide
  • Units affected: 8492 total units

The hazard

The products are contaminated with Salmonella. The FDA classified the recall as Class I, indicating a reasonable probability that the use of the product will cause serious adverse health consequences or death.

Context

GovInfoNow's records show Total Nutrition Inc has one other recall on record since May 22, 2026, involving Moringa Capsules and Salmonella contamination risk. Other recent recalls of similar products include Food to Live Organic Moringa Leaf Powder (Nov. 11, 2025), Bulk & Organic Moringa Powder (Oct. 31, 2025), and Trafa Organic Moringa Leaf Powder (June 24, 2026).

How to tell if you have this one

Check for product labels with 'Total Nutrition Inc' and the specific product names: Moringa Capsules (1,200 mg) or Moringa Powder (96 grams). The capsules have product number AB9917 and lot number 2800, expiring 2/2028. The powder has product number AB9904 and lot number 2782, expiring 5/2028.

  • Brand
    Total Nutrition
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Products

    Immediately stop using the recalled Moringa Capsules and Powder products to avoid potential Salmonella contamination.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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 33 days after the firm started it.

1. Firm started the recall: Jun 26, 202612. FDA classified it Class I: Jul 23, 202623. Published in FDA’s Enforcement Report: Jul 29, 202632026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-1185-2026 (June 26, 2026)
  • Plain-language summary written by qwen3:4b on August 18, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA