[ FDA ENFORCEMENT INTELLIGENCE ]
Learn from the record. Every FDA recall is a quality signal.
Live drug, device & food recall data from the FDA (openFDA enforcement) — food spanning dietary supplements, cosmetics & animal food — mapped to the GxP quality domains SPEQ assesses, so you can see where control breaks down across every regulated industry.
1,000
Total recalls
217
Class I (most serious)
167
Drug
515
Device
318
Food / supplement / cosmetic
Last 12 months · latest report 2026-07-22 · source: openFDA enforcement
RECALLS BY CLASSIFICATION · MONTHLY
RECALL REASONS BY QUALITY DOMAIN
Domain mapping is a SPEQ interpretation of the FDA recall reason, not an official FDA classification.
1,232 matching recalls
| Date | Class | Firm | Reason | Quality domain |
|---|---|---|---|---|
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0280-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0250-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | African Food on Wheels Inc.H-0237-2026 | Clostridium botulinum (uneviscerated fish) | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0257-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0299-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0297-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0255-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0263-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | Moonlight Packing CorporationH-0321-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
| 2025-12-17 | Class I | Moonlight Packing CorporationH-0318-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
| 2025-12-17 | Class I | ByHeart, INC.H-0249-2026 | Contaminated with Clostridium botulinum | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0283-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0262-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | Moonlight Packing CorporationH-0323-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0295-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0290-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0269-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0270-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0286-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0284-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0251-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0292-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0285-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0281-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | Moonlight Packing CorporationH-0324-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
Data: U.S. FDA openFDA enforcement API. Quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Recall details are as reported by the FDA.