Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Mariscos Bahia Inc is recalling fresh salmon fillet portions distributed to restaurants in Arizona and California due to possible Salmonella contamination. Approximately 179,002 pounds of product have been recalled.
Whole Foods Market is recalling Zerto Fontal Cheese due to undeclared egg allergen from egg lysozyme. Products were sold in Connecticut, New Jersey, and New York from September 7-29, 2022.
Mariscos Bahia Inc is recalling tuna fillets and loins due to possible salmonella contamination. The product was distributed to restaurants in Arizona and California.
Multiple brands of baked brie cheese are being recalled due to potential Listeria monocytogenes contamination. Products were distributed across multiple U.S. states and Mexico.
Old Europe Cheese, Inc. is recalling Reny Picot Apple Baked Brie due to potential Listeria monocytogenes contamination. The recall affects 1,309 pieces with best-by dates from September 28, 2022 to December 14, 2022.
Saint Louis Brie and related brie products have been recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,701 cases distributed to retailers in Louisiana, Maine, Missouri, North Carolina, and New York.
Baxter Healthcare is recalling the Hillrom WatchCare Incontinence Management System due to radio frequency emissions that may interfere with other critical medical devices including insulin pumps and fetal monitors.
Mariscos Bahia Inc recalls halibut fillets and portions due to possible salmonella contamination. Affected product was distributed to 179 restaurant customers in Arizona and California.
Hillrom Centrella Hospital Beds with WatchCare systems may emit radio frequency signals that interfere with other medical devices. Approximately 6,407 units are affected and distributed in the US.
Mariscos Bahia Inc is recalling Chilean Seabass fillets and portions due to possible salmonella contamination. The product was distributed to restaurants in Arizona and California.
Mariscos Bahia Inc is recalling swordfish products distributed to restaurants and food service businesses in Arizona and California due to possible salmonella contamination.
Holiday Rambler and Fleetwood motorhomes (2022–2023) have interior step treads that may be improperly secured and can detach when stepped on, creating a fall hazard.
The BD Nexiva Closed IV Catheter System tip shield may separate prematurely during needle withdrawal, leaving the needle tip exposed. This affects 56,080 units distributed across multiple U.S. states.
Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.
Domino Foods Inc is recalling Domino and C&H Granulated Pure Cane Sugar (Easy Baking Tub) due to potential contamination with metal wire from a broken screen. The recalled product was distributed to distribution centers in 22 states.
Multiple cottage cheese brands are recalled due to possible plastic foreign objects. The recall affects 391,824 cases distributed to 38 states.
HP Hood LLC is recalling Hood Cottage Cheese with Blueberries (16 oz) because the product may contain plastic pieces. Affected products have best-by dates between October 24, 2022 and December 12, 2022.
Becton Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together in pouches or fail when used with automated loaders. No illnesses have been reported.
HP Hood LLC is recalling Hood and Penn Maid cottage cheese with pineapple and cherry due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.
Vital Care Compounder is recalling Ceftazidime intravitreal injection solutions due to manufacturing conditions that cannot guarantee product sterility. Affected lots were distributed to patients in Alabama, Louisiana, Mississippi, and Tennessee.
A compounded injectable medication containing papaverine, phentolamine, and prostaglandin was recalled after FDA inspection found it was not produced under conditions that guarantee sterility. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.
Pharmacy Plus, Inc. recalled a compounded injectable medication (56 vials) due to manufacturing processes that cannot guarantee product sterility. Distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Vital Care Compounder is recalling 378 droptainers of PRED ACETATE/GATIFLOXACIN eye drops distributed in AL, LA, MS, and TN due to inability to guarantee manufacturing sterility. No illnesses have been reported.
Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.