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Consumer Product Recalls

127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.

March 25, 2025Vehicle EquipmentNHTSA
Lucid Vehicle Speed Control recall
Hazard: Unintended acceleration increases the risk of a crash.
March 24, 2025VehiclesNHTSA
Kenworth, Peterbilt 2020–2026 Electrical System recall
Hazard: A loss of drive power increases the risk of a crash.
March 24, 2025VehiclesNHTSA
Peterbilt, Kenworth 2021–2025 Electrical System recall
Hazard: A loss of drive power increases the risk of a crash.
March 24, 2025VehiclesNHTSA
Volvo 2020–2022 Electrical System recall
Hazard: A short circuit in a high-voltage battery increases the risk of a fire.
March 21, 2025VehiclesNHTSA
Winnebago 2025 Equipment recall
Hazard: Incorrect tire inflation information can result in improperly inflated tires and cause tire failure, increasing the risk of a crash.
March 21, 2025VehiclesNHTSA
International 2019–2025 Service Brakes, Air recall
Hazard: A loss of outer brake pad function can extend the vehicle's stopping distance, increasing the risk of a crash.
March 20, 2025VehiclesNHTSA
IC BUS 2025 Exterior Lighting recall
Hazard: Headlight low beam failure can reduce visibility, increasing the risk of a crash.
March 20, 2025VehiclesNHTSA
IC BUS 2025–2026 Exterior Lighting recall
Hazard: Headlight low beam failure can reduce visibility, increasing the risk of a crash.
March 20, 2025VehiclesNHTSA
Cadillac, Chevrolet 2016–2018 Steering recall
Hazard: A loss of power steering assist can require greater steering effort, especially at low speeds, increasing the risk of a crash.
March 20, 2025VehiclesNHTSA
Jeep 2024–2025 Exterior Lighting recall
Hazard: Incorrectly adjusted headlights can reduce driver visibility or create a glare for oncoming traffic, increasing the risk of a crash.
March 20, 2025VehiclesNHTSA
Thor Motor Coach 2023–2026 Equipment recall
Hazard: A slide-Out room that extends unexpectedly increases the risk of a crash.
March 20, 2025OtherCPSC
Arsell Recalls Benadryl Liquid Elixir 100 mL Bottle Due to Risk of Child Poisoning; Violation of Federal Regulation for Child Resistant Packaging; Sold on Amazon.com
Hazard: The Benadryl contains diphenhydramine, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
March 20, 2025Bikes & Recreational VehiclesCPSC
Segway Recalls Segway Ninebot Max G30P and Max G30LP KickScooters Due to Fall Hazard and Risk of Serious Injury
Hazard: The folding mechanism can fail and cause the handlebars or stem to fold while the scooter is in use, posing a fall hazard to consumers.
March 20, 2025FurnitureCPSC
GIKPAL Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violations of Federal Regulation for Clothing Storage Units; Sold Exclusively on Walmart.com by ONME Direct
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 violate performance and labeling requirements of the STURDY Act.
March 20, 2025AppliancesCPSC
Sensio Recalls Steam Espresso Machines Due to Burn and Laceration Hazards
Hazard: The brew cup handle can forcefully eject during use, shattering the glass carafe and posing a burn and laceration hazard.
March 20, 2025Electronics & BatteriesCPSC
VC Group Recalls Wireless Portable Power Banks with Lithium-Ion Batteries Due to Fire and Burn Hazards
Hazard: The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
March 20, 2025OtherCPSC
Woolite Delicates Detergent Recalled by Reckitt Due to Risk of Exposure to Bacteria; Sold Exclusively on Amazon.com
Hazard: The recalled products can contain Pseudomonas species bacteria, including Pseudomonas oleovorans, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to the bacteria face a risk of serious infection that may require medical treatment. The bacteria can enter the body through the eyes or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
March 20, 2025Bikes & Recreational VehiclesCPSC
Bombardier Recreational Products (BRP) Recalls Ski-Doo and Lynx Snowmobiles Due to Crash Hazard
Hazard: The engine control module (ECM) lower mount support could have broken in production and left a loose part inside the engine compartment, allowing it to enter the throttle body area and lead to a stuck throttle. This poses a crash hazard and risk of serious injuries or death.
March 20, 2025AppliancesCPSC
Aiper Seagull Pro Cordless Robotic Pool Vacuum Cleaners Recalled Due to Burn and Fire Hazards; Distributed by Shenzhen Aiper Intelligent Co.
Hazard: The recalled pool vacuum cleaner has a large current adapter that can overheat, posing burn and fire hazards.
March 20, 2025Sports & RecreationCPSC
Kimpex Recalls Snowmobile Ski and Adaptor Kits Due to Crash Hazard and Risk of Serious Injury
Hazard: The skis can detach from the snowmobile, posing a crash hazard and risk of serious injury.
March 20, 2025Sports & RecreationCPSC
Tzumi Electronics Recalls FitRx SmartBell XL Quick-Select Adjustable Dumbbells Due to Impact Injury Hazard; Sold Exclusively at Walmart.com
Hazard: Weight plates can dislodge from the dumbbell handle during use, posing an impact hazard to consumers.
March 19, 2025Medical DevicesFDA
Cordis US Corp recalls Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for int
Hazard: Catheter manufactured at the incorrect length.
March 19, 2025Medical DevicesFDA
Zimmer, Inc. recalls Z1 Femoral Hip System, Product Number 611777612
Hazard: There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.
March 19, 2025Medical DevicesFDA
Stryker Corporation recalls Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Hazard: Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment.
March 19, 2025Medical DevicesFDA
Spectrum Medical Inc recalls Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood, Cardiopulm
Hazard: Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.
March 19, 2025Medical DevicesFDA
Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
Hazard: The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash Wheel Dispense Arm Spin Mixer Error that is displayed on the navigation bar in the User Interface. The analyzer enters the red system status and will generate a SYS flag. The tests that are in progress may be cancelled and may cause a delay in reporting patient results
March 19, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software V
Hazard: Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
March 19, 2025Medical DevicesFDA
Philips Medical Systems Nederland B.V. recalls Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;
Hazard: Multiple problems identified with the software version leading to various scanning and image issues, and unintended device movement.
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80A; Software Version: NA Product Descrip
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4)
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).