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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
October 23, 2025Sports & RecreationCPSC
Lifepro Fitness Recalls Bioremedy Infrared Sauna Blankets Due to Risk of Burn Injuries
Hazard: The sauna blankets can overheat, posing a burn hazard.
October 23, 2025VehiclesNHTSA
Wartech 2022–2025 Service Brakes, Air recall
Hazard: An air leak can cause the unintentional activation of the brakes. Reduced brake pressure can increase the distance required to stop. Either scenario increases the risk of a crash.
October 23, 2025VehiclesNHTSA
Honda 2025 Power Train recall
Hazard: The inability to shift gears while riding increases the risk of a crash or injury.
October 23, 2025VehiclesNHTSA
Maserati 2023–2025 Exterior Lighting recall
Hazard: Improperly aimed headlights can result in insufficient illumination of the road, reducing the driver's visibility, and increasing the risk of a crash.
October 23, 2025VehiclesNHTSA
Ford 2021–2023 Seats recall
Hazard: A seat with a dislodged bolt may not properly restrain an occupant in a crash, increasing the risk of injury.
October 23, 2025VehiclesNHTSA
RAM 2018–2026 Engine And Engine Cooling recall
Hazard: Electrical circuits that overheat increase the risk of a fire.
October 22, 2025Medical DevicesFDA
Diagnostica Stago, Inc. recalls Product: STA Liatest D-Di; REF: 00515;
Hazard: A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SET, 96" (2,4 m), Product Code: 2H8519
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micro
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 me
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Filter, CLEARLINK Luer
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activated Valves, Backche
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activated Valves, Backcheck
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractab
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractab
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Prod
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product code
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock Extensio
Hazard: IV sets may leak.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits IHDC30R D AND C PACK
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits UDPG88W PICC G-TUBE PACK-230209
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description BFCT04X CATARACT PACK - 205986 CMEY17AI EYE PACK - 213187 CMEY17
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK - 205962 EVAH76H ANTERIOR HIP PACK FDSA15
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A DTC LAMINECTOMY PACK (PS 209475) RCN
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
October 22, 2025Medical DevicesFDA
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description FHCP08Y C SECTION PK HICS50I C-SECTION PACK HSCB90B C-SECTION BA
Hazard: Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.