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Stop using now Food recall · FDA · Published June 24, 2026

Trafa Organic Moringa Leaf Powder Recall: Salmonella Contamination Risk

Trafa Pharmaceuticals recalls 15kg organic moringa leaf powder with potential Salmonella contamination. Affected batches include brown paper bags with white label and batch #TRF-2025050801. Consumers should check their products for this specific batch.

🇺🇸 FDA recall #H-1144-2026FoodTrafa Pharmaceuticals ›
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Recalling firmTrafa Pharmaceutical Inc.140 Padgette St Ste D · Chicopee, MA 01022-1309
✎ GovInfoNow plain-language explainer

Trafa Pharmaceuticals is recalling 15kg organic moringa leaf powder due to potential Salmonella contamination. This could cause food poisoning if consumed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/6175-trafa-organic-moringa-leaf-powder-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6175-trafa-organic-moringa-leaf-powder-recall-salmonella-contamination-risk · Updated August 7, 2026 · Official notice: FDA #H-1144-2026

Cite this page

“Trafa Organic Moringa Leaf Powder Recall: Salmonella Contamination Risk.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6175-trafa-organic-moringa-leaf-powder-recall-salmonella-contamination-risk. Based on FDA recall #H-1144-2026.

The FDA announced on June 24, 2026, that Trafa Pharmaceutical Inc. is recalling its brand ORGANIC MORINGA LEAF POWDER due to potential Salmonella contamination. The voluntary Class I recall affects 500 kg of product distributed in New York.

How to tell if you have it

  • Brand: Trafa Pharmaceuticals
  • Product: ORGANIC MORINGA LEAF POWDER
  • Net Weight: 15 KGS
  • Packaging: Brown paper bags with a white label
  • Batch #: TRF-2025050801
  • Manufacturing Date: 2025-05-08
  • Restest Date: 2028-05-07

The hazard

The product poses a potential contamination with Salmonella. The FDA classified the recall as Class I, indicating a dangerous or defective product that could cause serious adverse health consequences or death.

Context

GovInfoNow's records show other recent recalls of similar products include Bulk & Organic Moringa Powder Recall: Possible Salmonella Richmond Risk (2025-10-31), Total Nutrition Moringa Capsules Recall: Salmonella Contamination Risk (2026-05-22), and Africa Imports Moringa Powder Recall: Salmonella Risk (2025-11-04).

How to tell if you have this one

Check for brown paper bags with a white label and batch number TRF-2025050801. The product was manufactured on May 8, 2025, and expires on May 7, 2028.

  • Brand
    Trafa Pharmaceuticals
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Product

    Immediately stop using the affected 15kg organic moringa leaf powder if you have it.

Where it went and when

Where it was distributed

Distributed in New York.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “NY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New York.

Recall timeline

FDA published this recall 21 days after the firm started it.

1. Firm started the recall: Jun 24, 202612. FDA classified it Class I: Jul 7, 202623. Published in FDA’s Enforcement Report: Jul 15, 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-1144-2026 (June 24, 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.
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