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FDA recall, , High risk

TNVitamins Organic Moringa Capsules and Powder

TNVitamins 100% Organic Moringa Capsules and Powder are contaminated with Salmonella, which can cause serious infections.

What happened

Total Nutrition Inc. of Deer Park, New York is voluntarily recalling TNVitamins 100% Organic Moringa Capsules 1,200 mg and 100% Organic Moringa Powder 96 grams following a supplier-initiated recall of the raw Organic Moringa ingredient because of possible Salmonella exposure. The recall was begun and announced on June 26, 2026, and was added to the FDA's Enforcement Report on July 23, 2026. The products were distributed nationwide, and no illnesses have been reported.

What to do

If a code on your package is listed below:

  1. Customers who have purchased the affected products are asked to dispose of them immediately.
  2. Do not eat, sell, or serve the product.
  3. For more information, please visit http://tnvitamins.com/organic-moringa-recall.
  4. For questions, please reach out to customerservice@tnvitamins.com.

Is yours affected?

Compare the details below with your product and check the FDA notice to confirm whether it is affected.

  1. Product details

    1. TNVitamins 100% Organic Moringa Capsules 1,200 mg
    2. TNVitamins 100% Organic Moringa Powder 96 grams

    Lot code
    • 2800
    • 2.Product
    • AB9904
    • 2782
  2. TNVitamins 100% Organic Moringa Capsules 1,200 mg

    Lot code
    • 2800
    Expiration date
    2/2028
  3. TNVitamins 100% Organic Moringa Powder

    Lot code
    • 2782
    Expiration date
    5/2028

Label photos, 4

Recall details

Company began the recall
Sold in
Nationwide
Company
Total Nutrition IncDeer Park, New York
Risk

High risk

There is a reasonable chance that taking it could cause serious health problems or death.

FDA Class I recall · How risk is rated

Event ID
99317
Recall number
H-1185-2026
Quantity recalled
8492 total units

All recalls from Total Nutrition Inc

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall · Announced by the company

  2. Listed on Recall Canary

  3. Added to FDA's Enforcement Report · Classified by FDA

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)