Fresh Recalls

FDAClass I · Food · Recall H-1144-2026 · Recalled July 15, 2026

Trafa Pharmaceuticals Inc recall — Trafa Pharmaceutical Inc.

Agency report date: July 15, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Trafa Pharmaceuticals Inc
Company / brand
Trafa Pharmaceutical
Lot / serial / date codes
BATCH #TRF-2025050801 MAN. DATE: 2025-05-08 RESTEST. DATE: 2028-05-07
Distribution
NY
Agency product description and boundaries

Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Potential contamination with Salmonella

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Trafa Pharmaceuticals Inc

3. Open the official notice or contact

Official recall ID
H-1144-2026
Brand
Trafa Pharmaceutical
Classification
Class I
Units affected
500 kg
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Chicopee, MA, United States
Firm address
140 Padgette St Ste D, N/A, 01022-1309

Identifying details (verbatim from the notice)

Product codes / lots
BATCH #TRF-2025050801 MAN. DATE: 2025-05-08 RESTEST. DATE: 2028-05-07
Distribution
NY
Firm notified the public via
E-Mail
FDA event ID
99314
Recall initiated
June 24, 2026
FDA classified
July 7, 2026
FDA report date
July 15, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page