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Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

May 21, 2026VehiclesNHTSA
Bentley 2026 Power Train recall
Hazard: A loose hub securing nut can cause vibration and a loss of steering control, increasing the risk of a crash.
May 21, 2026VehiclesNHTSA
Cadillac 2015–2016 Air Bags recall
Hazard: An inflator rupture may result in sharp metal fragments striking the driver or other occupants, resulting in serious injury or death.
May 21, 2026VehiclesNHTSA
Jeep 2022–2026 Air Bags recall
Hazard: Delayed air bag deployment during a crash increases the risk of injury.
May 21, 2026VehiclesNHTSA
Chrysler, Jeep, RAM 2019–2025 Back Over Prevention recall
Hazard: A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
May 21, 2026VehiclesNHTSA
Jeep 2026 Back Over Prevention recall
Hazard: A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
May 21, 2026VehiclesNHTSA
Chevrolet, GMC 2018–2019 Air Bags recall
Hazard: A detached end cap or inflator rupture can allow compressed gas to escape and project the end cap or fragments of the inflator into the vehicle, increasing the risk of injury.
May 21, 2026Lighting & ElectricalCPSC
Bethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC
Hazard: The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.
May 21, 2026Electronics & BatteriesCPSC
ABC Trading Recalls WSDZ Light-up Glasses Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
Hazard: The recalled glasses violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
May 21, 2026OtherCPSC
PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs
Hazard: The recalled portable hook-on chairs violate the mandatory standard for portable hook-on chairs because the crotch restraints can be removed without the use of a tool and infants can fall through an opening, posing a deadly fall hazard.
May 21, 2026Bikes & Recreational VehiclesCPSC
Lil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs
Hazard: The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical suspension requirements, and the reverse indicator light fails to illuminate, posing a crash hazard. The parking brakes fail to hold, posing a collision hazard. Additionally, the surfaces near the footwell can reach high temperatures, posing a risk of severe burns.
May 21, 2026ToysCPSC
Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
Hazard: The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.
May 21, 2026Sports & RecreationCPSC
Resistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym
Hazard: The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.
May 21, 2026ToysCPSC
ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
Hazard: The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
May 20, 2026Medical DevicesFDA
Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following device
Hazard: Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.
May 20, 2026Medical DevicesFDA
MICROVENTION INC. recalls LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22 m
Hazard: Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product
May 20, 2026Medical DevicesFDA
Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Hazard: Incomplete seals on sterile product