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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 17, 2025Vehicle EquipmentNHTSA
Cummins Fuel System, Diesel recall
Hazard: A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
January 16, 2025VehiclesNHTSA
Acura 2024 Electrical System recall
Hazard: Damaged high voltage cables or EV battery coolant lines can cause a loss of drive power, increasing the risk of a crash.
January 16, 2025VehiclesNHTSA
Jaguar 2019–2020 Back Over Prevention recall
Hazard: A rearview camera that does not display an image can reduce the driver's rear view, increasing the risk of a crash.
January 16, 2025VehiclesNHTSA
Land Rover 2023–2024 Equipment recall
Hazard: A rearview camera that does not display an image can reduce the driver's rear view, increasing the risk of a crash.
January 16, 2025VehiclesNHTSA
Gmc, Chevrolet 2024–2025 Seat Belts recall
Hazard: An improperly secured seat belt assembly may not restrain an occupant as intended, increasing the risk of injury in a crash.
January 16, 2025VehiclesNHTSA
Peterbilt, Kenworth 2023–2024 Vehicle Speed Control recall
Hazard: A pedal that sticks increases the risk of a crash.
January 16, 2025VehiclesNHTSA
Chevrolet 2025 Forward Collision Avoidance recall
Hazard: A vehicle that does not automatically brake as expected increases the risk of a crash.
January 16, 2025VehiclesNHTSA
RAM 2016–2020 Air Bags recall
Hazard: An inflator rupture may result in sharp metal fragments striking occupants, resulting in injury.
January 16, 2025Vehicle EquipmentNHTSA
Mopar Power Train recall
Hazard: A loss of drive power can increase the risk of a crash. A loss of park function can cause an unintended vehicle rollaway, which can increase the risk of a crash or injury.

January 16, 2025FurnitureCPSC
Veyer Recalls WorkPro Office Chairs Due to Fall Hazard
Hazard: The bolts that connect the back of the chair to its base can fail, posing a fall hazard to users.

January 16, 2025Clothing & AccessoriesCPSC
Ivy City Recalls Children's Pajamas Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively by Ivy City
Hazard: The recalled children's pajamas violate the flammability standards for children's sleepwear, posing a risk of burn injuries to children.

January 16, 2025Electronics & BatteriesCPSC
Three61 Recalls Samurai Mini Smoke Alarms Due to Failure to Alert Consumers to a Fire; Sold Exclusively by HSN
Hazard: The smoke alarms can malfunction and fail to alert consumers of a fire, posing a risk of smoke inhalation or death. Smoke sensitivity tests performed on the alarms by CPSC found that one of the detectors that was tested failed to alert when exposed to pre-determined concentrations of smoke.

January 16, 2025FurnitureCPSC
HallyBee Farmhouse Dressers Recalled Due Tip-Over and Entrapment Hazards; Violation of Federal Regulation for Clothing Storage Units; Sold Exclusively on Amazon.com by YKHallyBee
Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers do not comply with the performance requirements of the STURDY Act.

January 16, 2025AppliancesCPSC
Vornado Air Recalls VH2 Whole Room Heaters Due to Electric Shock and Fire Hazards; Sold Exclusively on Amazon.com
Hazard: The power cord can partially detach from the heater enclosure, which can lead to cord damage over time, posing electric shock and fire hazards.

January 16, 2025Bikes & Recreational VehiclesCPSC
Polaris Industries Recalls Model Year 2024-2025 Ranger XD 1500 and Crew XD 1500 Recreational Off-Road Vehicles (ROVs) Due to Injury and Crash Hazards
Hazard: The door handle can stick and cause the door to unexpectedly open while the vehicle is moving and cause an unrestrained rider to be ejected from the vehicle or increase the risk of a crash, posing serious injury and crash hazards.

January 16, 2025OtherCPSC
Northern Tool + Equipment Recalls Adjustable Swivel Shop Stools with Backrests Due to Fall Hazard
Hazard: The welded connection point between the seat base and the stool post can break, presenting a fall hazard.

January 16, 2025OtherCPSC
Lexmark International Recalls Specialty Printers Due to Fire Hazard
Hazard: A metal part inside the printer can dislodge, posing a risk of fire.
January 15, 2025Medical DevicesFDA
3B Medical, Inc. recalls Brand Name: 3B Medical, Inc. Product Name: Ultrasoft Oxygen Cannula, 12 Foot Model / Catalog Number: O2U2012 Lot Numb
Hazard: The devices were inadvertently shipped after their expiration date.
January 15, 2025Medical DevicesFDA
Nipro Renal Soultions USA, Corporation recalls Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Hazard: The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
January 15, 2025Medical DevicesFDA
Applied Medical Technology Inc recalls AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Hazard: The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV
Hazard: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO
Hazard: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV
Hazard: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
Hazard: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610
Hazard: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3
Hazard: GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12; 2) 5555000-5; 3)
Hazard: GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.
January 15, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3)
Hazard: GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.
January 15, 2025Medical DevicesFDA
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.
Hazard: Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.
January 15, 2025Medical DevicesFDA
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Hazard: Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts; necessary clinical intervention could be delayed.