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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
December 12, 2025VehiclesNHTSA
Ford 2026 Power Train recall
Hazard: A broken rear axle shaft can result in a loss of drive power or vehicle rollaway when the vehicle is placed in park. Either of these scenarios can increase the risk of a crash.
December 12, 2025VehiclesNHTSA
Mercedes-benz 2025 Electrical System recall
Hazard: A loss of drive power can increase the risk of a crash.
December 12, 2025VehiclesNHTSA
Mercedes-benz 2025–2026 Seat Belts recall
Hazard: In the event of a crash, an insufficiently restrained child has an increased risk of injury.
December 12, 2025VehiclesNHTSA
Ford 2022–2026 Power Train recall
Hazard: A loss of park function can allow the vehicle to rollaway, increasing the risk of a crash.
December 12, 2025VehiclesNHTSA
Lincoln, Ford 2025–2026 Seat Belts recall
Hazard: An improperly secured seat belt retractor may not restrain an occupant as intended, increasing the risk of injury during a crash.
December 12, 2025VehiclesNHTSA
Diamond Coach 2025 Equipment Adaptive/Mobility recall
Hazard: An unsecured wheelchair can move during transit, increasing the risk of injury.
December 12, 2025VehiclesNHTSA
Ford 2022–2025 Power Train recall
Hazard: A loss of drive power increases the risk of a crash. In addition, a half shaft that is not fully engaged to the primary drive unit can result in a vehicle rollaway if the parking brake is not applied, increasing the risk of a crash or injury.

December 11, 2025Bikes & Recreational VehiclesCPSC
Luyuan Recalls Youth ATVs Due to Risk of Serious Injury or Death from Crash Hazard; Violate Mandatory Standard for All-Terrain Vehicles
Hazard: The recalled youth ATVs violate the mandatory ATV safety standard. The youth ATVs' mechanical suspension fails to comply with safety requirements, posing a crash hazard. Additionally, the handlebars pose a laceration hazard, if the child rider's body or head impacts the handlebars at high speed. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury or death.

December 11, 2025OtherCPSC
Sanven Technology Recalls Vevor Ice Crushers Due to Fire Hazard
Hazard: The ice crusher can experience a thermal event and ignite, posing a fire hazard.

December 11, 2025Children's ProductsCPSC
YCXXKJ Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by BenTalk
Hazard: The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.

December 11, 2025Clothing & AccessoriesCPSC
Sanven Technology Recalls VEVOR Steamers Due to Risk of Serious Injury from Burn Hazard
Hazard: The steamers can leak or spit hot water, posing a risk of serious burn injury to users and bystanders. The water tank cap can also leak or detach during use, exposing users to hot water.

December 11, 2025Children's ProductsCPSC
Uuoeebb Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by BaoD
Hazard: The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.

December 11, 2025OtherCPSC
SKCAIHT Children's Costumes Recalled Due to Risk of Injury from Phthalate Exposure; Violates Federal Phthalates Ban; Sold on Amazon by SKCAIHT Direct
Hazard: The children's costumes contain a prohibited phthalate, which violates the federal phthalates ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.

December 11, 2025Children's ProductsCPSC
Primark Recalls Little Bear 2-Pack Soother Clips Due to Choking and Laceration Hazards
Hazard: The wooden button on the soother clips can come off, exposing a sharp screw, which can pose choking and laceration hazards.

December 11, 2025Bikes & Recreational VehiclesCPSC
TREK Recalls Electric Bicycles Due to Fall or Crash Hazard
Hazard: The bolts on the chainring can come loose, causing the chainring to separate from the bike, resulting in a fall or crash hazard to the user.
December 11, 2025VehiclesNHTSA
Acura 2016–2020 Service Brakes, Hydraulic recall
Hazard: Reduced brake function can extend the distance required to stop, increasing the risk of a crash or injury.
December 11, 2025VehiclesNHTSA
Honda 2025 Electrical System recall
Hazard: An internal short circuit in a fuel cell can cause a loss of drive power, increasing the risk of a crash or injury.
December 11, 2025VehiclesNHTSA
BMW 2025–2026 Steering recall
Hazard: Unintended steering wheel movement while the vehicle is stationary increases the risk of an injury and on the road, a crash.
December 11, 2025VehiclesNHTSA
GMC 2024–2026 Air Bags recall
Hazard: An air bag that deploys improperly increases the risk of injury in a crash.
December 11, 2025Vehicle EquipmentNHTSA
Q Straint Equipment Adaptive/Mobility recall
Hazard: An unsecured wheelchair can move during transit, increasing the risk of injury.
December 10, 2025Medical DevicesFDA
Illumina, Inc. recalls Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5
Hazard: An instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow cell gaskets that have a quality issue, which may lead to flow cell leaks during runs, which could cause run failures, that may result in: No/insufficient data output, instrument fluidics clogs, toxic substance exposure to user.
December 10, 2025Medical DevicesFDA
Philips Ultrasound, LLC recalls Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Hazard: Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls CT 5300; Software Version Number: 4.5, 5.0, 5.1;
Hazard: If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within the Incisive CT systems during rotation. Other components could be damaged due to the contact with the tube heat exchanger.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls Incisive CT; Software Version Number: 4.5, 5.0, 5.1;
Hazard: If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within the Incisive CT systems during rotation. Other components could be damaged due to the contact with the tube heat exchanger.
December 10, 2025Medical DevicesFDA
Accriva Diagnostics, Inc. recalls Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Who
Hazard: Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected prior to handling.
December 10, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAMMOMAT Fusion;
Hazard: There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
December 10, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAMMOMAT Inspiration;
Hazard: There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
December 10, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAMMOMAT Revelation;
Hazard: There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
December 10, 2025Medical DevicesFDA
Microbiologics Inc recalls KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Hazard: Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
December 10, 2025Medical DevicesFDA
Aizu Olympus Co., Ltd. recalls Olympus OER-Mini
Hazard: Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.