[ 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.

1,475 matching recalls

Date	Class	Firm	Reason	Quality domain
2026-02-11	Class II	Organic Spices, IncH-0465-2026	Product contains salt and is mislabeled	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0474-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	Everpress JuiceH-0453-2026	Under-processed product may contain pathogenic bacteria that could harm to humans.	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0470-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	VENZU TRADERS LLCH-0466-2026	Potential contamination with heavy metal (lead).	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0476-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0473-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Organic Spices, IncH-0464-2026	Product contains salt and is mislabeled	Documentation & Change Control
2026-02-11	Class II	WinCo Foods LLCH-0449-2026	Product may contain foreign material (metal fragments).	Environmental Monitoring
2026-02-11	Class III	Optiwize Inc.H-0442-2026	The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity.	Documentation & Change Control
2026-02-11	Class III	Prima Foods International, Inc.H-0445-2026	Undeclared Quinine	Documentation & Change Control
2026-02-11	Class I	B.C. Williams Bakery Service, IncH-0500-2026	Undeclared Milk Allergen	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0479-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class III	Prima Foods International, Inc.H-0446-2026	Undeclared Quinine	Documentation & Change Control
2026-02-11	Class III	Prima Foods International, Inc.H-0447-2026	Undeclared Quinine	Documentation & Change Control
2026-02-11	Class I	Tradin Organics USA LLCH-0460-2026	Potential contamination with Salmonella.	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0471-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	Everpress JuiceH-0454-2026	Under-processed product may contain pathogenic bacteria that could harm to humans.	Environmental Monitoring
2026-02-11	Class III	Prima Foods International, Inc.H-0448-2026	Undeclared Quinine	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0475-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	Everpress JuiceH-0452-2026	Under-processed product may contain pathogenic bacteria that could harm to humans.	Environmental Monitoring
2026-02-11	Class I	B.C. Williams Bakery Service, IncH-0501-2026	Undeclared Milk Allergen	Documentation & Change Control
2026-02-11	Class I	B.C. Williams Bakery Service, IncH-0499-2026	Undeclared Milk Allergen	Documentation & Change Control
2026-02-11	Class III	Willy Pete's Chocolate Company LLCH-0484-2026	Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.	Documentation & Change Control
2026-02-11	Class III	Prima Foods International, Inc.H-0443-2026	Undeclared Quinine	Documentation & Change Control

Page 28 of 59

← Prev Next →

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.