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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 18, 2026DrugsFDA
Pro Numb Tattoo Numbing Spray LLC recalls Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed
Hazard: cGMP deviations
February 18, 2026DrugsFDA
Pro Numb Tattoo Numbing Spray LLC recalls Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tatto
Hazard: cGMP deviations
February 18, 2026VehiclesNHTSA
Lexus 2025–2026 Power Train recall
Hazard: A damaged transmission can cause a loss of drive power, increasing the risk of a crash. In addition, a damaged transmission can leak transmission fluid, increasing the risk of a fire.
February 17, 2026VehiclesNHTSA
Prevost 2025–2026 Seats recall
Hazard: An improperly installed seat anchor may not adequately restrain the seat occupant, increasing the risk of injury during a crash.
February 17, 2026VehiclesNHTSA
Ford, Lincoln 2022–2026 Electrical System recall
Hazard: Battery failure can cause a loss of drive power, increasing the risk of a crash. Battery failure can also increase the risk of a fire.
February 17, 2026VehiclesNHTSA
Ford 2025 Service Brakes, Hydraulic recall
Hazard: A loss of brake function increases the risk of a crash.
February 17, 2026VehiclesNHTSA
Winnebago 2020–2023 Structure recall
Hazard: A detached roof cap can become a road hazard for other vehicles and increase the risk of a crash.
February 17, 2026VehiclesNHTSA
Blue ARC 2024–2025 Steering recall
Hazard: Binding in the gearbox can cause a loss of steering, increasing the risk of a crash.
February 13, 2026VehiclesNHTSA
Thomas Built Buses 2023–2026 Engine And Engine Cooling recall
Hazard: Contact with hot heating coolant may burn occupants, increasing the risk of injury.
February 13, 2026VehiclesNHTSA
Thomas Built Buses 2023–2026 Engine And Engine Cooling recall
Hazard: Contact with hot heating coolant may burn occupants, increasing the risk of injury.
February 13, 2026VehiclesNHTSA
Cadillac, Chevrolet, GMC 2022 Power Train recall
Hazard: Rear wheels that lock up while driving increase the risk of a crash.
February 13, 2026Vehicle EquipmentNHTSA
Hyperax Equipment recall
Hazard: A detached carrier or bike can become a road hazard for other vehicles, increasing the risk of a crash or injury.
February 12, 2026VehiclesNHTSA
International 2026–2027 Forward Collision Avoidance recall
Hazard: A vehicle that does not automatically brake as expected increases the risk of a crash.
February 12, 2026VehiclesNHTSA
Chevrolet, GMC 2020–2022 Power Train recall
Hazard: Rear wheel lock up increases the risk of a crash.
February 12, 2026VehiclesNHTSA
Cadillac 2024 Back Over Prevention recall
Hazard: An inoperative rearview camera can reduce the driver's rear visibility, increasing the risk of a crash.
February 12, 2026OtherCPSC
Watkins Manufacturing Recalls Hydromassage Rotary Jets in Highlife Collection Spas Due to Entanglement and Drowning Hazards
Hazard: The hydromassage rotary jets can create a suction force that allows the user's hair to be entangled, submerging their head underwater, posing entanglement and drowning hazards to the user.
February 12, 2026FurnitureCPSC
Beloems Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.
February 12, 2026Children's ProductsCPSC
CheerKid Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violates Mandatory Standard for Infant Bath Seats; Sold on Amazon by Babibaby and Woot
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.
February 12, 2026ToysCPSC
Surveying Accessories Cheaper Recalls Board Games Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Hazard: The recalled board games violate the mandatory standard for toys because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
February 12, 2026FurnitureCPSC
Fortemotus Direct Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.
February 12, 2026FurnitureCPSC
SOOWERY 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
February 12, 2026Fire & SafetyCPSC
LShome Photoelectric Smoke Detector Fire Alarms Recalled Due Failure to Warn During Fire Posing Serious Injury or Death Hazard; Sold Exclusively on Amazon.com by TIANJINSHIHAOWEIXINSHENGJIDIANANZHUANGGONGCHENG
Hazard: If the sensing threshold of security warnings is set too high, the alarm might not sound in a timely manner, posing a fire hazard.
February 11, 2026Medical DevicesFDA
ETAC A/S recalls Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mobile hoists) Model/Catalog Number: 1430116,
Hazard: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
February 11, 2026Medical DevicesFDA
ETAC A/S recalls Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 153
Hazard: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
February 11, 2026Medical DevicesFDA
ETAC A/S recalls Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050,
Hazard: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
February 11, 2026Medical DevicesFDA
ETAC A/S recalls Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050,
Hazard: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
February 11, 2026Medical DevicesFDA
Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Produc
Hazard: Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
February 11, 2026Medical DevicesFDA
Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Software Version: Not Appli
Hazard: Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
February 11, 2026Medical DevicesFDA
Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Vers
Hazard: Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
February 11, 2026Medical DevicesFDA
Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Product
Hazard: Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).