[ 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
2026-06-24Class IIIUnited Salt CorpH-0952-2026Plain salt was labeled as iodized and iodized salt was labeled as plain.Documentation & Change Control
2026-06-24Class IIMID DOLCIARIA SRLH-0945-2026The product contains unapproved colors chlorophyll E140 and E141.Documentation & Change Control
2026-06-24Class IAzuma Foods International Inc USAH-1075-2026Undeclared fish.Documentation & Change Control
2026-06-24Class IIInternational Food Products CorporationH-1076-2026Product tested positive for SalmonellaEnvironmental Monitoring
2026-06-24Class IGREENWORLD FOOD EXPRESS (USA) LLCH-0950-2026Product may be contaminated with SalmonellaEnvironmental Monitoring
2026-06-24Class IIDkiru LLCH-1079-2026Undeclared melatonin.Documentation & Change Control
2026-06-24Class IIInternational Food Products CorporationH-1077-2026Potential for SalmonellaEnvironmental Monitoring
2026-06-17Class IIGalaxy RG CorpH-0928-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IKettle Cuisine, LLCH-0941-2026Contains undeclared allergen (shrimp).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0931-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0915-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0916-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0923-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IHH FRESH TRADING CORPH-0939-2026Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.Environmental Monitoring
2026-06-17Class IIGalaxy RG CorpH-0933-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIRich Products CorpH-0912-2026May contain metal pieces—
2026-06-17Class IIGalaxy RG CorpH-0922-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0934-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0917-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIU.S. Tov, Inc. dba U.S. Trading CompanyH-0943-2026Potential contamination with lead.Environmental Monitoring
2026-06-17Class IIIMothers' Milk Bank of Louisiana at Ochsner BaptistH-0938-2026Potential physical contamination: dark spot was noticed on the bottom of container.Environmental Monitoring
2026-06-17Class IIIWeikfield Foods Pvt. Ltd.H-0911-2026The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.Documentation & Change Control
2026-06-17Class IIIRefresqueria Estrella Inc.H-0913-2026Undeclared FD&C Red 40Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0936-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).Documentation & Change Control
2026-06-17Class IIGalaxy RG CorpH-0926-2026Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).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.