[ 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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1,496 matching recalls
DateClassFirmReasonQuality domain
2026-04-15Class IIIMEI YU CHENG DA TRADING INCH-0657-2026Products contain banned sweetener: cyclamates.—
2026-04-15Class IPure Vitamins and Natural Supplements, LLCH-0653-2026FDA analysis revealed the presence of undeclared sildenafil and TadalafilDocumentation & Change Control
2026-04-15Class IIZarlengo Italian IceH-0651-2026Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.—
2026-04-15Class IAYCO FARMS INCH-0668-2026Potential Salmonella ContaminationEnvironmental Monitoring
2026-04-15Class IIIMEI YU CHENG DA TRADING INCH-0658-2026Products contain banned sweetener: cyclamates.—
2026-04-08Class IIIPocas International Corp.H-0633-2026Packaging integrity issue that may compromise product quality .Documentation & Change Control
2026-04-08Class IIISuper World Trading Inc.H-0641-2026Products contain cyclamates (banned sweetener)—
2026-04-08Class IIIPocas International Corp.H-0635-2026Packaging integrity issue that may compromise product quality .Documentation & Change Control
2026-04-08Class IIImu-Tek Animal Health, IncorporatedH-0660-2026Product is potentially under-processed.Risk Management & CAPA
2026-04-08Class IIHEYTEA USA INCH-0646-2026Product contains undeclared milk.Documentation & Change Control
2026-04-08Class IIThe Maros Group, LLCH-0644-2026Undeclared sulfites.Documentation & Change Control
2026-04-08Class IITG FOODS INCH-0637-2026The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.—
2026-04-08Class IIImu-Tek Animal Health, IncorporatedH-0661-2026Product is potentially under-processed.Risk Management & CAPA
2026-04-08Class IIISuper World Trading Inc.H-0642-2026Products contain cyclamates (banned sweetener)—
2026-04-08Class IIISuper World Trading Inc.H-0643-2026Products contain cyclamates (banned sweetener)—
2026-04-08Class IIIPocas International Corp.H-0636-2026Packaging integrity issue that may compromise product quality .Documentation & Change Control
2026-04-08Class IIJFE FRANCHISING INCH-0639-2026Foreign Object (Glass)Environmental Monitoring
2026-04-08Class IIIPocas International Corp.H-0634-2026Packaging integrity issue that may compromise product quality .Documentation & Change Control
2026-04-08Class IIJFE FRANCHISING INCH-0638-2026Foreign Object (Glass)Environmental Monitoring
2026-04-08Class ILone Star Dairy Products LLCH-0640-2026Salmonella spp. identified in finished product testingEnvironmental Monitoring
2026-04-08Class IIThe Maros Group, LLCH-0645-2026Undeclared milk.Documentation & Change Control
2026-04-01Class IIMangalm LLCH-0628-2026Potential adulteration with erucic acid from mustard oil ingredient.Risk Management & CAPA
2026-04-01Class IIAjinomoto Foods North America Inc.H-0599-2026Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.Environmental Monitoring
2026-04-01Class IIAjinomoto Foods North America Inc.H-0596-2026Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.Environmental Monitoring
2026-04-01Class IIRose and Shore, Inc.H-0622-2026potential foreign object (metal pieces) in ingredient (Tomatoes)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.