[ 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 | Moonlight Packing CorporationH-0322-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0268-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0259-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0254-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0275-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0300-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0282-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0289-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0266-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class II | Santos Agency Inc.H-0304-2026 | Potential contamination due to leachable lead. | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0253-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0264-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0288-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0276-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0293-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0298-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0256-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0258-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0287-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0291-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | Moonlight Packing CorporationH-0320-2026 | Potential contamination with Listeria monocytogenes. | Environmental Monitoring |
| 2025-12-17 | Class III | Glenmark Pharmaceuticals Inc., USAD-0222-2026 | Cross Contamination with Other Products | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0278-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0252-2026 | Product tested positive Salmonella . | Environmental Monitoring |
| 2025-12-17 | Class I | CHETAK NEW YORK LLCH-0279-2026 | Product tested positive Salmonella . | 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.