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Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

December 18, 2025VehiclesNHTSA
Honda 2024–2026 Engine And Engine Cooling recall
Hazard: Rear wheel lockup increases the risk of a crash or injury. Engine oil that leaks onto hot exhaust components increases the risk of a fire.
December 18, 2025VehiclesNHTSA
Altec 2023–2025 Exterior Lighting recall
Hazard: Wiring without adequate protection may short circuit, increasing the risk of a fire.
December 18, 2025VehiclesNHTSA
Subaru 2026 Structure recall
Hazard: A rear hatch support bracket that detaches can allow the rear hatch to fall unexpectedly during use and increase the risk of injury.
December 18, 2025VehiclesNHTSA
Ford 2021–2022 Back Over Prevention recall
Hazard: A rearview image that continues to be displayed after the vehicle is shifted out of reverse may distract the driver, increasing the risk of a crash.
December 18, 2025VehiclesNHTSA
Ford 2022 Back Over Prevention recall
Hazard: A camera that does not display a rearview image while reversing can reduce the driver's view of what is behind the vehicle, increasing the risk of a crash.
December 18, 2025VehiclesNHTSA
Ford 2019 Electrical System recall
Hazard: If the driver exits the vehicle without the transmission being shifted into park, unintended vehicle movement may result, increasing the risk of injury or crash.
December 18, 2025VehiclesNHTSA
Ford 2025–2026 Exterior Lighting recall
Hazard: A loss of exterior lighting can reduce the driver's visibility and the visibility of the vehicle to other drivers, increasing the risk of a crash.
December 18, 2025VehiclesNHTSA
Ford 2025–2026 Structure recall
Hazard: An instrument panel cover separation can cause pieces of the cover to strike occupants, increasing the risk injury during a crash.
December 18, 2025VehiclesNHTSA
RAM 2025 Air Bags recall
Hazard: Driving with a disabled electronic stability control system increases the risk of a crash. Additionally, a driver's side air bag or seat belt pretensioner that does not deploy increases the risk of injury in a crash.
December 18, 2025VehiclesNHTSA
Ford 2020–2024 Power Train recall
Hazard: A loss of drive power increases the risk of a crash.
December 18, 2025VehiclesNHTSA
IC BUS 2026 Equipment Adaptive/Mobility recall
Hazard: An unsecured wheelchair can move during transit, increasing the risk of injury.
December 18, 2025VehiclesNHTSA
IC BUS 2026–2027 Equipment Adaptive/Mobility recall
Hazard: An unsecured wheelchair can move during transit, increasing the risk of injury.
December 18, 2025VehiclesNHTSA
Chevrolet 2025–2026 Back Over Prevention recall
Hazard: A vehicle that does not emit sufficient sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.
December 18, 2025Vehicle EquipmentNHTSA
Mobis Trailer Hitches recall
Hazard: Nonfunctioning trailer lights can increase the risk of a crash. A short circuit can increase the risk of a fire.
December 18, 2025Vehicle EquipmentNHTSA
Mopar Air Bags recall
Hazard: Driving with a disabled electronic stability control system increases the risk of a crash. Additionally, a driver's side air bag or seat belt pretensioner that does not deploy increases the risk of injury in a crash.
December 17, 2025Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Stryker Arise 1000EX mattress, Part Number 2236000000
Hazard: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
December 17, 2025Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Stryker MV3 bariatric bed, Part Number 5900000001
Hazard: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
December 17, 2025Medical DevicesFDA
Datascope Corp. recalls Cardiosave Rescue. Intra-Aortic Balloon Pump system.
Hazard: The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
December 17, 2025Medical DevicesFDA
Datascope Corp. recalls Cardiosave Hybrid. Intra-Aortic Balloon Pump system.
Hazard: The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
December 17, 2025Medical DevicesFDA
Nipro Medical Corporation recalls Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Hazard: Screw may loosen or fallout of Hemodialysis system
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls DEXLOCK Achilles Repair Implant Kits, MAKT4520
Hazard: There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.
December 17, 2025Medical DevicesFDA
Steris Corporation recalls AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfec
Hazard: Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
December 17, 2025Medical DevicesFDA
Steris Corporation recalls AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfect
Hazard: Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
C.R. Bard Inc recalls Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
Hazard: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.