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
Porsche is recalling 2020-2023 Taycan models due to a malfunctioning seat belt warning system that may fail to alert unbelted passengers. Dealers will update the instrument cluster software free of charge.
Kia is recalling 2022-2023 Carnival vehicles with tow hitch harnesses that may accumulate water, causing electrical shorts that can result in fire.
Kia is recalling certain 2022 Sorento vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase the risk of engine fire.
The tire placard label on certain 2023-2024 Alfa Romeo Tonale and Dodge Hornet vehicles displays an incorrect maximum vehicle capacity weight value, which could lead to vehicle overloading and increased crash risk. Dealers will add an overlay label to correct the information.
Heartland is recalling 2021-2022 North Trail trailers because the Gross Axle Weight Rating on the federal certification label is incorrect, risking vehicle overloading and crashes.
True Manufacturing is recalling about 29,200 commercial refrigerators equipped with Secop compressors that can overheat and catch fire. The firm has received 14 reports of fires causing property damage, with no injuries reported.
Dixon Ticonderoga is recalling Creativity Street Foam Pattern Rollers because the handles contain lead levels above the federal limit. Lead is toxic if ingested by young children and can cause adverse health effects.
Arctic Cat is recalling approximately 16,200 model year 2017–2021 and certain 2022 snowmobiles from the 8000 and 9000 series because the drive clutch can break and allow fragments to escape the shielding, causing laceration injuries.
SKIMS is recalling about 1,200 children's fleece pajama sets that fail to meet federal flammability regulations for children's sleepwear, posing a risk of burn injuries. Consumers should stop using them immediately and contact SKIMS for a refund.
Certain 2022 Mercedes-Benz Sprinter vehicles with adjustable front swivel-seats have wiring harnesses that may be incorrectly installed, causing side airbags to fail deployment in a crash and increasing injury risk.
Igloo Products is recalling about 31,500 Youth Sipper Bottles because the silicone cover on the sipper can detach while in use, posing a choking hazard to children. One incident was reported, but no injuries have occurred.
BMW is recalling 2023 and some 2022 model-year vehicles for a software defect allowing power windows and sunroofs to close without the digital key present, posing a risk of injury to occupants.
Polaris is recalling about 240 Model Year 2024 Prostar S4 Titan Adventure 155 ES Snowmobiles because the fuel pump flange assembly can leak fuel, creating a fire hazard and risk of serious injury. No injuries have been reported.
2019–2021 Mercedes-Benz G550 and AMG G63 models may lose anti-lock brakes and stability control due to front axle wiring harness chafing against the oil cooler, increasing crash risk.
American Honda Motor is recalling lawnmowers and replacement engines with faulty camshafts that can cause the starter rope to suddenly retract, injuring users. About 200 additional replacement engines are included in this expansion of a previous recall.
LFN Limited is recalling about 200 Mill Valley Jr. six-drawer youth dressers sold at Rooms To Go from December 2023 through January 2024 due to tip-over and entrapment hazards if not anchored to the wall. No injuries have been reported.
Bausch + Lomb is recalling about 32,000 units of Project Watson Eyelid Wipes for Dogs due to risk of bacterial and fungal growth in the container after opening, which could cause serious infection in immunocompromised people or those with wounds.
Alcoholada Gel pain reliever is being recalled because the ethanol ingredient contains methanol contamination. The FDA classified this as a Class I recall affecting 9,625 bottles distributed nationwide.
Pyramids Wholesale Inc. is recalling Silverback XXX Power male enhancement nationwide due to undeclared sildenafil and/or tadalafil. These prescription drugs were not approved by the FDA before marketing.
Route 92 Medical 070 Access System catheters are recalled for potential distal tip separation during neurovasculature procedures. The defect affects 117 units distributed across 30 US states and New Zealand.
Route 92 Medical's Full Length 070 Access System (REF 7002) is recalled due to potential distal tip separation at the proximal marker band of the delivery catheters. This FDA Class I recall affects a device used in neurovasculature interventions distributed across the US and New Zealand.
The GOAT Sublingual Strip male enhancement product, distributed nationwide, was recalled for containing undeclared sildenafil and tadalafil. The product was marketed without FDA approval.
Pyramids Wholesale Inc. is recalling Pink Pussycat Honey because it contains undeclared sildenafil and tadalafil and was marketed without FDA approval. The recall affects all lots nationwide.
ForeverMen Natural Energy Boost Capsules contain undeclared sildenafil and are marketed without FDA approval, making them an unapproved drug. Consumers should stop using the product immediately.
Flower Power CBD infused Female Enhancement contains undeclared sildenafil and tadalafil. These prescription drugs were not disclosed to consumers and the product was marketed without FDA approval.