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 deaths or serious injuries are reported, 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
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.
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 swordfish products distributed to restaurants and food service businesses in Arizona and California due to possible salmonella contamination.
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.
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.
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.
Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.
Power Plus is recalling about 115 Tora portable power charging stations because the lithium-ion battery can catch fire while charging. Two fires have been reported with no injuries.
Earth Grown Vegan Traditional Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The FDA Class I recall affects approximately 190,860 units distributed across multiple U.S. states.
Cut Fruit Express is recalling Caribou Coffee Snack Fruit and Cheese Plates due to potential Listeria in the Brie cheese. Affected units were distributed in Minnesota with Use By dates from September 30 to October 9, 2022.
Earth Grown Vegan Garlic & Herb Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The recall affects over 190,000 units distributed across multiple US states.
Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.
Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.
Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.
Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.
Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.
Goalsetter is recalling about 18,000 wall-mounted basketball goals because they can detach from walls and fall. One fatality and multiple injuries have been reported.
Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.
LG Energy Solution is recalling about 11,500 RESU 10H lithium-ion residential energy storage batteries because they can overheat and pose a fire risk with harmful smoke emissions. One incident of smoking and fire with property damage has been reported.
Catheter mounts with filters (REF 191667-000100) used to connect endotracheal tubes or masks to breathing circuits may split or detach during patient use. Teleflex is recalling affected units distributed nationwide.
TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.