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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 20, 2026VehiclesNHTSA
Ford 2017–2019 Suspension recall
Hazard: A rear toe link fracture can result in a loss of steering control, increasing the risk of a crash.
February 20, 2026VehiclesNHTSA
Rossmonster 2023–2025 Service Brakes, Hydraulic recall
Hazard: A brake fluid leak can decrease braking performance, increasing the risk of a crash.
February 20, 2026VehiclesNHTSA
Mercedes-benz 2025 Back Over Prevention recall
Hazard: Insufficient pedestrian warning sounds may fail to alert pedestrians of an approaching vehicle, increasing the risk of injury.
February 20, 2026VehiclesNHTSA
Demers Ambulances 2025–2026 Seats recall
Hazard: Structural failure may prevent the seat from properly restraining an occupant during a crash, increasing the risk of injury.
February 19, 2026VehiclesNHTSA
Land Rover 2023–2026 Structure recall
Hazard: A detached panoramic sunroof side trim can become a road hazard, increasing the risk of injury or crash.
February 19, 2026VehiclesNHTSA
BMW 2023–2026 Electrical System recall
Hazard: A damaged wiring harness can short-circuit, increasing the risk of a fire.
February 19, 2026VehiclesNHTSA
Prevost 2026 Visibility recall
Hazard: A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.
February 19, 2026Vehicle EquipmentNHTSA
Prevost Visibility recall
Hazard: A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.

February 19, 2026Bikes & Recreational VehiclesCPSC
SAMIT Youth Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by SAMIT Outdoor
Hazard: The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

February 19, 2026FurnitureCPSC
Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging
Hazard: The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

February 19, 2026Children's ProductsCPSC
Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
Hazard: The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.

February 19, 2026Electronics & BatteriesCPSC
JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Hazard: The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

February 19, 2026OtherCPSC
Joly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
Hazard: The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.

February 19, 2026ToysCPSC
Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
Hazard: The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

February 19, 2026FurnitureCPSC
Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, 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. In addition, the bed rails do not bear the required hazard warning labels.
February 18, 2026Medical DevicesFDA
Steris Corporation recalls Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H
Hazard: This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.
February 18, 2026Medical DevicesFDA
SUREPULSE MEDICAL LTD recalls Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor
Hazard: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
February 18, 2026Medical DevicesFDA
SUREPULSE MEDICAL LTD recalls Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor
Hazard: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
February 18, 2026Medical DevicesFDA
SUREPULSE MEDICAL LTD recalls Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor
Hazard: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
February 18, 2026Medical DevicesFDA
SUREPULSE MEDICAL LTD recalls Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor
Hazard: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
February 18, 2026Medical DevicesFDA
SUREPULSE MEDICAL LTD recalls Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor
Hazard: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
February 18, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45
Hazard: Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, instruments remain active, could lead to instrument contact with tissue, resulting in injury/bleeding; may require alternate surgical modality.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions:
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - Al
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number -
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
February 18, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X,
Hazard: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.