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.
Milk Wash packed exclusively for Chick-fil-A is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.
Meatloaf seasoning packed for the Costco service deli is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.
Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.
Erbe Medical is recalling ERBEFLO 2 Endoscopy Pump Tubing/Cap Sets due to a connector design that may allow unintended water flow, potentially leading to water aspiration and serious respiratory conditions.
Medline Industries is recalling multiple surgical convenience kits because equipment used to sterilize and package the devices had calibration issues that may have affected sterility assurance. The devices were processed through validated sterilization cycles but the calibration problems could impact their sterility.
Milk-N-Egg Mix in 50 lb bags is being recalled after the firm was notified by its supplier that the nonfat dry milk may be contaminated with Salmonella. 833 bags are affected.
Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
Loard's Vanilla Ice Cream in 32 oz and 56 oz containers is being recalled because it contains milk that is not listed on the label.
Loard's Rocky Road Ice Cream in 56 oz tubs is being recalled because milk, walnuts and eggs are undeclared on the label. 516 units are affected.
Silver Moon LP dba Loard's Ice Cream is voluntarily recalling Loard's Chocolate Ice Cream because it contains undeclared milk.
Loard's Cookies and Cream Ice Cream in 32 oz and 56 oz tubs is being recalled because milk, wheat and soy are undeclared on the label.
Loard's Peppermint Ice Cream in 32 oz and 56 oz tubs is being recalled because milk, soy and Red #40 are undeclared on the label.
Natural Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.
Loard's Maple Walnut Ice Cream in 32 oz tubs is being recalled because milk, walnuts and sulfites are undeclared on the label. 405 units are affected.
Erbe Medical is recalling ERBEFLO CleverCap hybrid tubing and cap sets for endoscopes due to a connector configuration that may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
Medline is recalling Basic Nerve Block Trays due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the devices.
Loard's Coffee Ice Cream in 32 oz tubs is being recalled because milk is undeclared on the label. 790 units are affected.
Loard's Toasted Almond Ice Cream in 32 oz tubs is being recalled because milk and almonds are undeclared on the label. 656 units are affected.
Medline Industries is recalling multiple Convenience Kits nationwide because sterilization equipment calibration issues may have compromised the sterility assurance level of the products, despite exposure to validated sterilization cycles.
Cinnamon Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.
Physio-Control defibrillators (LIFEPAK 15, 1000, 35, and 20e models) serviced between July 2023 and November 2025 may not have undergone required Performance Inspection Procedures, potentially preventing therapy delivery.
Medline is recalling two models of Convenience Kits because calibration issues with sterilization and packaging equipment may have compromised the sterility assurance level of the devices.
Medline is recalling five models of arthroscopy convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Medline is recalling Convenience Kits (Model DYNJ50806L) because equipment calibration issues may have affected the sterility assurance level of the devices. The products were exposed to sterilization and packaging cycles but the calibration problems could impact their sterility.
Montebianco Base Vegan is being recalled because the milk allergen present was found to exceed acceptable levels despite the product carrying only a "May contain milk" statement.