[ 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.

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1,232 matching recalls
DateClassFirmReasonQuality domain
2025-12-17Class IMoonlight Packing CorporationH-0314-2026Potential contamination with Listeria monocytogenes.Environmental Monitoring
2025-12-17Class IIIndia's Fine Foods, Inc.H-0242-2026Potential contamination due to leachable lead.Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0287-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0285-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0281-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class IMoonlight Packing CorporationH-0324-2026Potential contamination with Listeria monocytogenes.Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0301-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0296-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class IIIGlenmark Pharmaceuticals Inc., USAD-0222-2026Cross Contamination with Other ProductsEnvironmental Monitoring
2025-12-17Class IIIndia's Fine Foods, Inc.H-0243-2026Potential contamination due to leachable lead.Environmental Monitoring
2025-12-17Class ICHETAK NEW YORK LLCH-0267-2026Product tested positive Salmonella .Environmental Monitoring
2025-12-17Class IMoonlight Packing CorporationH-0319-2026Potential contamination with Listeria monocytogenes.Environmental Monitoring
2025-12-10Class IILaiwu Manhing Vegetables Fruits CoH-0232-2026foreign objects (black plastic planting film) in granulated onion powderEnvironmental Monitoring
2025-12-10Class IIGreat Lakes Cheese Co IncH-0218-2026Potential metal fragments from supplier raw material (downstream recall)Environmental Monitoring
2025-12-10Class IAfrica ImportsH-0222-2026Product tested positive for Salmonella.Environmental Monitoring
2025-12-10Class IIGreat Lakes Cheese Co IncH-0217-2026Potential metal fragments from supplier raw material (downstream recall)Environmental Monitoring
2025-12-10Class IIHale incH-0240-2026Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.Environmental Monitoring
2025-12-10Class IIGreat Lakes Cheese Co IncH-0221-2026Potential metal fragments from supplier raw material (downstream recall)Environmental Monitoring
2025-12-10Class IIITriple B CorporationH-0365-2026Potential chemical contamination.Environmental Monitoring
2025-12-10Class IAmerican Nuts, LLCH-0228-2026Potential Salmonella contamination.Environmental Monitoring
2025-12-10Class IIWater Pure, Inc.H-0213-2026Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303Environmental Monitoring
2025-12-10Class IIGreat Lakes Cheese Co IncH-0220-2026Potential metal fragments from supplier raw material (downstream recall)Environmental Monitoring
2025-12-10Class IIVENTURA FOODS LLCH-0236-2026foreign objects (black plastic planting material) in granulated onionEnvironmental Monitoring
2025-12-10Class IIGreat Lakes Cheese Co IncH-0215-2026Potential metal fragments from supplier raw material (downstream recall)Environmental Monitoring
2025-12-10Class IINutrition for LongevityH-0231-2026Potential contamination with Listeria monocytogenes.Environmental Monitoring
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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.