Agency
The FDA regulates food, drugs, biologics, medical devices, and tobacco. We aggregate Class I, II, and III enforcement actions across its three recall streams.
The FDA is the single biggest source of US product recalls by volume. Its enforcement workload splits into three streams — Foods (everything from infant formula to leafy greens to nutritional supplements), Drugs (prescription medicines, over-the-counter products, and active pharmaceutical ingredients), and Medical Devices (everything from implants to home blood-pressure monitors). The Recall Desk ingests all three from the openFDA enforcement endpoint every six hours.
FDA classifies every recall as Class I, II, or III. Class I means there is a reasonable probability that using the product will cause serious health consequences or death — these are the recalls you should treat as urgent. Class II means the product may cause temporary or medically reversible harm. Class III means the product is unlikely to cause adverse health consequences but still violates FDA rules. We map these classifications into our 1–5 severity score using the rubric on the methodology page.
Medical-device recalls are the highest-volume stream by far — software-update letters, calibration corrections, and IFU updates all show up in enforcement reports alongside genuine hazard recalls. We try to surface the severe ones first, but when in doubt, click through to the FDA notice itself for the clinical detail.
Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen val papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen arvi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen green chili cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen dum aloo after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen ginger garlic cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen ratalu sliced violet Indian yams after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen sweet corn after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Boss Dairy Farms is recalling 420 units of Charlevoix Cheese Company Mild Cheddar Cheese over possible Listeria monocytogenes contamination. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen green garlic after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen tuvar lilva after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen garlic quick cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen diced bottle gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen bhindi cut okra after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 237,656 cases of loose bulk yellow peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 46,048 cases of 2 lb bagged peaches, including Kroger-distributed packs, over potential contamination with Listeria monocytogenes.
Chetak New York is recalling Deep-brand frozen snake gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,375 cases of loose bulk white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen red pearl onions after the product tested positive for Salmonella. The FDA has classified the action as Class I.
African Food on Wheels is recalling 20 boxes of oven dried fish over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen falsa after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen guvar after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Stuffed Foods is recalling 51 cases of Cacio e Pepe Arancini over undeclared soy protein concentrate. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen diced tapioca after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 13,069 cases of 4 lb Peppermint Peach white peaches over potential contamination with Listeria monocytogenes.