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

February 20, 2025OtherCPSC
Shadeks Recalls ShadesU Roller Window Shades Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violation of Federal Regulations for Window Coverings; Sold Exclusively on Amazon.com
Hazard: The recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard. The window blinds also violate federal regulations for labeling of window coverings.

February 20, 2025Children's ProductsCPSC
SuperATV Recalls Carrier Bearings for Polaris RZR XP and Turbo S Recreational Off Highway Vehicles Due to Fire and Burn Hazards
Hazard: When the recalled carrier bearings are installed in a Polaris RZR XP Turbo or Turbo S vehicle and the fuel tank expands, the drive shaft can come in contact with the fuel tank, causing the tank to develop a hole or crack. This can cause the fuel tank to leak gasoline, posing fire and burn hazards.

February 20, 2025Bikes & Recreational VehiclesCPSC
Super73 Recalls Z Miami SE and Z Adventure Core Electric Bicycles Due to Crash and Injury Hazards
Hazard: The retaining pin in the e-bike's disc brake calipers can loosen and dislodge from the caliper assembly, resulting in brake failure, posing crash and injury hazards to the rider.

February 20, 2025OtherCPSC
Homebox Blackout Roller Window Shades Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violation of Federal Regulations for Window Coverings; Sold Exclusively on Amazon.com by Zhejiang Mingjing Textile Co.
Hazard: The recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard. The window blinds also violate federal regulations for labeling of window coverings.

February 20, 2025FurnitureCPSC
Sauder Woodworking Recalls Clothing Storage Unit Tip-Over Restraint Straps Due to Tip-Over and Entrapment Hazards to Children
Hazard: The tip-over restraint straps can fail when used on certain Sauder clothing storage units (dressers and 4-drawer chests) to prevent tip-over incidents, posing tip-over and entrapment hazards that can result in death or serious injuries to children.

February 20, 2025FurnitureCPSC
SEJOV Dressers Recalled Due to Tip-Over and Entrapment Hazards; Violation of Federal Regulation for Clothing Storage Units; Sold on Amazon by SEJOV
Hazard: The recalled dressers are unstable if they are not properly 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 warning label requirements of the STURDY Act.
February 20, 2025Bikes & Recreational VehiclesCPSC
Triumph TF250-X Off-Road Motorcycles Recalled Due to Injury Hazard; Imported by Triumph Motorcycles America
Hazard: The right-hand plastic switch cube can crack when exposed to brake fluid, causing a short circuit that starts the motorcycle unexpectedly, posing an injury hazard.

February 20, 2025Electronics & BatteriesCPSC
Holosun Technologies Recalls Two Firearm Dot Sights Due to Battery Ingestion Hazard; Violations of Reese's Law Federal Safety Regulations for Consumer Products with Coin Batteries and Child Resistant Coin Battery Packaging
Hazard: The recalled Holosun Red and Gold Firearm Dot Sights violate the mandatory federal regulations for consumer products containing button cell or coin batteries because the lithium coin battery can be easily accessed, posing an ingestion hazard. The products include a lithium coin battery which is not in child-resistant packaging, as required by Reese's Law. In addition, the products do not bear the required warnings. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

February 20, 2025Electronics & BatteriesCPSC
Fjorden iPhone Camera Grips Recalled Due to Battery Ingestion Hazard; Violation of Reese's Law Federal Safety Regulations for Consumer Products with Coin Batteries; Sold Exclusively on shop.fjorden.co by Fjorden Electra AS
Hazard: The recalled camera grips violate the mandatory federal regulation for consumer products containing button cell and coin batteries because, when the product is dropped, the battery tray can separate from its compartment, making the lithium coin battery easily accessible by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
February 20, 2025OtherCPSC
Kubota Recalls Utility Tractors Due to Crash Hazard
Hazard: The clutch cable can break on the recalled MX5400DTC utility tractors, resulting in reduced braking power, posing a crash hazard.
February 20, 2025AppliancesCPSC
DR Power Equipment Recalls Tow Behind Field & Brush Mowers Due to Laceration Hazard
Hazard: The blade carrier spindle bolt can become loose, causing the blade assembly to detach while the mower is in operation, posing a laceration hazard to the user.

February 20, 2025ToysCPSC
Nazzaro Recalls Children Bowling Pin Sipper Cups Due to Risk of Lead Poisoning; Violation of Federal Lead Content Ban
Hazard: The red tape on the bowling pin sipper cups contains levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.

February 20, 2025Electronics & BatteriesCPSC
Walmart Recalls Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters with Lithium-Ion Batteries Due to Fire and Burn Hazards; Risk of Serious Injury and Death
Hazard: The electric scooters' lithium-ion batteries can overheat, smoke, melt and ignite, posing fire and burn hazards, posing a risk of serious injury and death.

February 20, 2025Bikes & Recreational VehiclesCPSC
Trek Recalls Electra E-Bikes Due to Crash Hazard
Hazard: The rear fender can come loose and can contact the rear wheel and stop the bike unexpectedly, causing the rider to lose control of the bike, posing a crash hazard.
February 19, 2025Medical DevicesFDA
Hologic, Inc recalls Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device Model/Catalog Number: Sertera-14 Software Versi
Hazard: Devices presented a condition in which the inner needle separated from the hub and produced a longer throw of the inner needle or dislodgement.
February 19, 2025Medical DevicesFDA
Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
Hazard: A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system.
February 19, 2025Medical DevicesFDA
Integra LifeSciences Corp. recalls Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software Ve
Hazard: Potential that the induction seal is not completely sealed to the device tube packaging.
February 19, 2025Medical DevicesFDA
Exactech, Inc. recalls Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL NTL LNR G00 22MM 140-28-50 NV EHXLNTRL LNR G0 28MM
Hazard: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
February 19, 2025Medical DevicesFDA
Exactech, Inc. recalls Novation XLE Item Number / Product Description: 140-22-70 NV EHXL NTL LNR G00 22MM 140-28-50 NV EHXLNTRL LNR G0 28MM
Hazard: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
February 19, 2025Medical DevicesFDA
Exactech, Inc. recalls AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL 0¿ LNR G 28MM 140-32-27 AM EHXL 0¿ LNR G 32MM 140-
Hazard: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
February 19, 2025Medical DevicesFDA
Microbiologics Inc recalls Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel (Inactivated Pellet), REF 8235; in-vitro diagn
Hazard: Internal quality control procedures were not followed correctly for the testing/release of three lots of 8234/8235. This resulted in the release of products that should have failed and been discarded. The concentration of one target (HPV 16 L1) was low enough to cause QC failures, no detection, or invalid results on some instruments and assays.
February 19, 2025Medical DevicesFDA
Microbiologics Inc recalls Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel (Inactivated Pellet), REF 8234; in-vitro diagnostic
Hazard: Internal quality control procedures were not followed correctly for the testing/release of three lots of 8234/8235. This resulted in the release of products that should have failed and been discarded. The concentration of one target (HPV 16 L1) was low enough to cause QC failures, no detection, or invalid results on some instruments and assays.
February 19, 2025Medical DevicesFDA
Elekta, Inc. recalls MOSAIQ Oncology Information System
Hazard: Image offsets calculated by oncology Information System software may be incorrect for Linear Accelerator (LINACs) not characterized at IEC61217 scale.
February 19, 2025Medical DevicesFDA
HF Acquisition Co LLC recalls Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In
Hazard: Spore test strip monitoring system, designed for routine monitoring of sterilization processes, may have a printing error on the return envelope that may cause spore test results to be reported to the incorrect customer's account.
February 19, 2025Medical DevicesFDA
Angel Medical Systems, Inc. recalls Brand Name: The Guardian System Product Name: The Guardian Model/Catalog Number: Model AMSG3-E Product Description: The
Hazard: Device reaching End of Service prematurely.
February 19, 2025Medical DevicesFDA
Stryker Corporation recalls stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades
Hazard: Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
February 19, 2025Medical DevicesFDA
Stryker Corporation recalls stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades
Hazard: Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) ACDF PACK, Catalog Number: SNEHBACSCA; 2) ACDF PACK, Catalog Number: SNEHBACSCB
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVA; 2) OPHTHALMOLOGY ENDO DC
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) CHI STD SPINE OPTION 1, Catalog Number:CHIP99SP11; 2) CHI STD SPINE OPTION 1, Catalog
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.