Food recall
Trafa Pharmaceutical Inc. recall: Trafa Pharmaceuticals Inc
Trafa Pharmaceutical Inc., of Chicopee, MA, recalled Trafa Pharmaceuticals Inc. The FDA's reason: “Potential contamination with Salmonella.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on June 24, 2026, and the FDA first listed it in its Enforcement Report of July 15, 2026. The recall is still going on.
How serious
Class I
It could cause serious harm or death
Why
Salmonella
Status
Ongoing
The recall
- Company
- Trafa Pharmaceutical Inc. (Chicopee, MA)
- Reason, in FDA's words
- “Potential contamination with Salmonella”
- Where it was sold
- NY
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 99314
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
H-1144-2026 Class I
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
Codes: BATCH #TRF-2025050801 MAN. DATE: 2025-05-08 RESTEST. DATE: 2028-05-07
Quantity: 500 kg
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 15, 2026.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.