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
The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate during medical procedures, potentially delaying treatment or requiring unplanned intervention. The recall affects 471 units distributed worldwide.
Cordis US Corp is recalling the ANGIOGUARD RX / XP Emboli Capture Guidewire System because the device may separate during procedures, risking stroke or requiring emergency intervention.
Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.
Meijer Inc. is recalling Fresh From Meijer Chicken Caesar Salads (6.4 oz and 10 oz sizes) due to potential Listeria monocytogenes contamination. Products were distributed to Meijer stores in six states: Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.
Revolution Farms is recalling Traverse City Cherry 6-ounce salad kits due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.
Ford is recalling certain 2023 F-250, F-350, and F-450 Super Duty vehicles due to loose or missing steering column bolts that could cause steering column separation, increasing the risk of crashes due to loss of steering control.
Forest River is recalling 2022-2023 Rockport work trucks because the trailer brake controller may be incorrectly wired, which can cause a loss of brake function and increase crash risk.
BMW is recalling 2007-2014 MINI Cooper models because a short-circuit in the driver's footwell may cause a fire. Owners should contact dealers for inspection and repair.
BRP U.S. Inc. is recalling about 12,500 Ski-Doo snowmobiles from model years 2021 and 2022 because a fuel injector hose retainer screw can loosen, cause fuel leaks, and pose a fire hazard. Four fires have been reported.
Dennis Eagle is recalling 2020-2023 ProView vehicles because the HVAC electrical circuit may overheat, increasing the risk of a fire.
Eastern Meat Solutions is recalling approximately 40,763 pounds of raw, boneless pork products imported from Canada without FSIS import reinspection. No adverse reactions have been reported.
Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.
Chrysler is recalling 2014-2016 Jeep Cherokee vehicles with power liftgates due to an electrical short that may cause a fire. Owners should park outside until repairs are completed.
Tandoori Peanut Spread is being recalled due to undeclared milk allergen. The product poses a risk to consumers with milk allergies.
Tandoori Roasted Chana (chickpeas) from Jabsons Foods is recalled because it contains undeclared milk, a major allergen. Consumers with milk allergies should not consume this product.
General Motors is recalling 2014-2017 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.
Mitten Gourmet is recalling approximately 1,137 pounds of ready-to-eat pork rinds because they were produced without the benefit of federal inspection. Consumers are urged to discard or return the products.
Salento Organics is recalling Dark Chocolate Peanut Bites due to undeclared milk. Consumers with milk allergies should not consume this product.
Tandoori Roasted Peanuts in 4.94 oz pouches are recalled due to undeclared milk. Consumers with milk allergies should not consume the product.
The FDA recalls NUX Male Enhancement capsules distributed nationwide because they contain undeclared sildenafil and tadalafil, making them an unapproved drug. Consumers should not use this product.
Salento Organics Dark Chocolate Mango Bites are recalled due to undeclared milk, which poses a risk to consumers with milk allergies.
Salento Organics has recalled Dark Chocolate Pineapple Bites due to undeclared milk. The affected product contains milk not identified on the label, posing a risk to consumers with milk allergies.
Jabsons Foods is recalling Thai sweet Chilli Roasted Peanut due to undeclared milk. The recall affects 508 cases distributed domestically in the United States.
Pro Power Knight Plus capsules contain undeclared sildenafil and tadalafil, prescription ingredients not listed on the label. The product was marketed as an unapproved drug and poses safety risks.