[ 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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743 matching recalls
DateClassFirmReasonQuality domain
2025-08-27Class IHillside Orchard Farms Inc.H-0515-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0511-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0516-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IIBuffalo Rock Company IncH-0504-2025Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar productDocumentation & Change Control
2025-08-27Class IISRI SRI TATTVAH-0505-2025Product contains undeclared soy lecithin.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0512-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IIKobayashi Noodle U.S.A.H-0502-2025Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0510-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0509-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IIKobayashi Noodle U.S.A.H-0503-2025Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.Documentation & Change Control
2025-08-27Class IIGriffith Foods Inc.H-0522-2025Undeclared eggsDocumentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0518-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0507-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0506-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0517-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0513-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0514-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0508-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IHillside Orchard Farms Inc.H-0519-2025Undeclared egg.Documentation & Change Control
2025-08-27Class IIIHaleon US Holdings LLCD-0592-2025Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer cartonDocumentation & Change Control
2025-08-20Class IITropicale Foods, LLCH-0465-2025Product label includes the ingredient CREAM but does not include Milk as the source.Documentation & Change Control
2025-08-20Class IITropicale Foods, LLCH-0464-2025Product label includes the ingredient CREAM but does not include Milk as the source.Documentation & Change Control
2025-08-20Class IITropicale Foods, LLCH-0467-2025Product label includes the ingredient CREAM but does not include Milk as the source.Documentation & Change Control
2025-08-20Class IITropicale Foods, LLCH-0463-2025Product label includes the ingredient CREAM but does not include Milk as the source.Documentation & Change Control
2025-08-20Class IITropicale Foods, LLCH-0462-2025Product label includes the ingredient CREAM but does not include Milk as the source.Documentation & Change Control
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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.