[ 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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1,235 matching recalls
DateClassFirmReasonQuality domain
2026-07-01Class ISpring & Mulberry Inc.H-1098-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1105-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1097-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1116-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1096-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1115-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class ICareFusion 213, LLCD-0624-2026Non-Sterility: Due to presence of Aspergillus penicillioides.Environmental Monitoring
2026-07-01Class IIChampion Foods, LLCH-1095-2026potential salmonella contaminationEnvironmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1112-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1117-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class IICareFusion 213, LLCD-0623-2026Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.Environmental Monitoring
2026-07-01Class IPrime Food Processing LLC.H-1080-2026Improperly eviscerated which may result in Clostridium botulinum contaminationEnvironmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1104-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1113-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class IUtz Quality Foods, LLCH-1114-2026Potential presence of Salmonella.Environmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1102-2026Potential Salmonella contamination.Environmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1099-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1101-2026Potential Salmonella contamination.Environmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1100-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1106-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class IICareFusion 213, LLCD-0622-2026Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.Environmental Monitoring
2026-07-01Class ISpring & Mulberry Inc.H-1103-2026Potential Salmonella contaminationEnvironmental Monitoring
2026-07-01Class IIPReye LLCD-0621-2026Lack of Assurance of SterilityEnvironmental Monitoring
2026-07-01Class ICareFusion 213, LLCD-0625-2026Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.Environmental Monitoring
2026-07-01Class IIDexcom, Inc.Z-2574-2026Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and distributors by Pharmsource, LLC. Lot 1725204004 were designated for destruction because the G7 sensors were not properly sterilized and have an increased risk of skin infection if used. Lot 1725069002 were designated for destruction due to an increased risk of having no sensor readings available or experiencing sensor inaccuracy that includes the potential for missed detection of a hyperglycemic event or incorrect treatment decisions that can result in patient injury, including medical intervention to prevent permanent injury or impairment. Additionally, due to the unknown storage and handling and storage conditions these sensors may have undergone during the distribution, these sensors may present additional risk.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.