[ 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 I	Everpress JuiceH-0456-2026	Under-processed product may contain pathogenic bacteria that could harm to humans.	Environmental Monitoring
2026-02-11	Class III	Prima Foods International, Inc.H-0444-2026	Undeclared Quinine	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0468-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0480-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	Everpress JuiceH-0455-2026	Under-processed product may contain pathogenic bacteria that could harm to humans.	Environmental Monitoring
2026-02-11	Class II	Khee Trading, Inc.H-0482-2026	Imported oysters potentially contaminated with Norovirus	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0477-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Imu-Tek Animal Health, IncorporatedH-0483-2026	Undeclared milk allergen	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0467-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0476-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	VH FOODS INCH-0481-2026	Undeclared allergens: egg and milk	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0478-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Diva Fam IncH-0469-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class I	Tai Phat Wholesalers, LLCH-0459-2026	Undeclared sulfites	Documentation & Change Control
2026-02-11	Class II	Beacon Promotions IncH-0462-2026	Undeclared allergens (milk, soy, and peanut)	Documentation & Change Control
2026-02-11	Class II	Diva Fam IncH-0472-2026	potential Clostridium botulinum contamination	Environmental Monitoring
2026-02-11	Class II	Rich Products CorpH-0440-2026	Product contains undeclared milk and egg	Documentation & Change Control
2026-02-04	Class II	Weaver's Brew LLCH-0436-2026	Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.	Risk Management & CAPA
2026-02-04	Class I	SUPERFOODS, INC.H-0433-2026	Products may be contaminated with Salmonella Typhimurium	Environmental Monitoring
2026-02-04	Class II	Plant Based Innovations, LLCH-0421-2026	Contains undeclared Almonds	Documentation & Change Control
2026-02-04	Class II	Weaver's Brew LLCH-0435-2026	Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.	Risk Management & CAPA
2026-02-04	Class I	SUPERFOODS, INC.H-0434-2026	Products may be contaminated with Salmonella Typhimurium	Environmental Monitoring
2026-02-04	Class III	NEW WAY IMPORT INCH-0420-2026	Undeclared allergen ingredient (wheat).	Documentation & Change Control
2026-02-04	Class II	Prima Vera Nueva, Inc.H-0426-2026	Potential contamination with biological hazards (Listeria monocytogenes).	Environmental Monitoring
2026-02-04	Class II	QUTEN RESEARCH INSTITIUTE LLCH-0418-2026	Mold contamination detected for raw material lots that were produced in July and used in finished goods.	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.