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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
March 14, 2025VehiclesNHTSA
Ford 2025 Back Over Prevention recall
Hazard: An inverted rearview camera image will not accurately display what is behind the vehicle, increasing the risk of a crash or injury.
March 14, 2025VehiclesNHTSA
Ford 2021–2022 Back Over Prevention recall
Hazard: A rearview camera that displays a blank or distorted image can reduce the driver's view of what is behind the vehicle, increasing the risk of a crash.
March 14, 2025VehiclesNHTSA
Lincoln, Ford 2020–2023 Back Over Prevention recall
Hazard: Loss of the rearview camera image can reduce the driver's rear visibility, increasing the risk of a crash.
March 14, 2025VehiclesNHTSA
Ford 2021–2024 Power Train recall
Hazard: An undetected low battery charge can result in a loss of electrical accessories such as hazard lights, or cause a loss of drive power, increasing the risk of a crash.
March 14, 2025VehiclesNHTSA
Ford 2023 Visibility recall
Hazard: A window that does not automatically reverse when an obstruction is encountered increases the risk of injury.
March 14, 2025Car SeatsNHTSA
Evenflo Child Seat recall
Hazard: A missing recall registration card may result in an unregistered child seat, which can delay recall notification and increase the risk of injury.
March 13, 2025VehiclesNHTSA
Brightdrop 2023–2024 Steering recall
Hazard: Steering lock up increases the risk of a crash.
March 13, 2025Vehicle EquipmentNHTSA
Zoox 2023–2024 Electrical System recall
Hazard: Unexpected hard braking can increase the risk of a crash.

March 13, 2025Kitchen & DiningCPSC
Gerolsteiner Sparkling Water Bottles Recalled Due to Laceration Hazard; Manufactured by Gerolsteiner
Hazard: The recalled water bottles can crack, causing a laceration hazard.

March 13, 2025Children's ProductsCPSC
Onasti Toddler Tower Stools Recalled Due to Serious Fall and Injury Hazards; Sold Exclusively on Amazon.com by Blissful-Time
Hazard: The stools can collapse or tip over while in use, posing serious fall and injury hazards to children.

March 13, 2025Sports & RecreationCPSC
Black Diamond Equipment Recalls BD Vision Climbing Harnesses Due to Fall Hazard; Risk of Serious Injury and Death
Hazard: The recalled BD Vision harnesses can degrade over time and fail to support the climber, posing a fall hazard resulting in serious injury or death.

March 13, 2025Children's ProductsCPSC
Chews Life Recalls Silicone Rosary and Decade Teethers Due to Choking Hazard
Hazard: Part of the teethers' safety snap clasp can detach, posing a choking hazard.

March 13, 2025OtherCPSC
Meijer Recalls Konwin Desktop Heaters Due to Fire and Burn Hazards
Hazard: The heater's fan can fail to turn on and cause the unit to overheat and ignite, posing fire and burn hazards.

March 13, 2025Children's ProductsCPSC
Safety Gates Recalled Due to Risk of Serious Injury or Death to Children from Entrapment Hazard; Violation of Federal Regulation for Gates and Enclosures; Sold Exclusively on Amazon.com by HabiLife Direct
Hazard: The recalled gates violate the federal safety regulations for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment hazard.

March 13, 2025Bikes & Recreational VehiclesCPSC
BMC Recalls Kaius 01 Bicycles and Framesets Due to Fall Hazard
Hazard: The fork steerer tube on the recalled bicycles and framesets can crack, break, or separate during use, posing a fall hazard.

March 13, 2025Electronics & BatteriesCPSC
Sublue Recalls Lithium-Ion Batteries Sold for Sublue Mix Underwater Scooters Due to Fire Hazard
Hazard: The lithium-ion batteries can overheat and ignite, posing a fire hazard to consumers.
March 12, 2025Medical DevicesFDA
Becton Dickinson & Co. recalls BD BBL TB Stain Kit K, Catalog (REF): 212522
Hazard: One component of the kit was shipped with an expiration date of 30Sep2024 while the Certificate of Analysis (COA) indicated an expiration date of 30Apr2025.
March 12, 2025Medical DevicesFDA
Integra LifeSciences Corp. recalls AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's Produ
Hazard: Possibility for the obturator to break (separate).
March 12, 2025Medical DevicesFDA
TAS Medical Inc recalls TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP
Hazard: Tissue approximation straps (zip-ties) have broken before or during implantation so firm developed an interim zip-tie conditioning method submerging zip-ties in 104-degrees F sterile saline solution for 60 min prior to implantation to rehydrate the zip-tie straps. Broken zip-ties not observed during procedure could lead to future hernia recurrence, recurrent surgery to correct a large herniation.
March 12, 2025Medical DevicesFDA
Alcon Research LLC recalls Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-
Hazard: Customer-designed sterile surgical procedure packs contain latex components as specified; but, the content label sealed within the transparent sterile pouch contains the symbol for a latex-free product. If users or patients with latex sensitivity come into contact with latex, an allergic reaction may occur.
March 12, 2025Medical DevicesFDA
Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050
Hazard: Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.
March 12, 2025Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal REF 71-C5100NS Tubing, Suction, Connector; DeRoyal REF 71-C6100NS Tubing, Suction, Connector; DeRoyal REF 71-C
Hazard: Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a suction canister lid port difficult. This could result in inadequate suction and cause a delay in patient care.
March 12, 2025Medical DevicesFDA
LUMENIS, LTD. recalls (1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, La
Hazard: The initial current in certain chargers may lead to overheating and damage to the power resistors on the Alternating Current (AC) controller during the power-on sequence of the laser system, resulting in the laser system to not power on.
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is intended for use with a dental implan
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prostheti
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is intended for use with a dental implan
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended for use with a dental implant to provide support for prosthet
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthet
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Hiossen Inc. recalls ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended for use with a dental implant to provide support for prosthet
Hazard: Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version
March 12, 2025Medical DevicesFDA
Telcare, LLC recalls Philips Connected Blood Glucose Meter, BGM 4; Model Number: TM0009;
Hazard: Telcare, LLC has received customer complaints related to battery expansion/swelling for its Philips Connected Blood Glucose Meter (i.e., BGM 4 brand name) Monitoring System.. The issue was identified by post market surveillance data (customer complaints) - events of battery expansion/swelling and associated symptoms, e.g., leading to the device's removable back cover (battery port) to separate. If there is a loss of primary function of the device due to the described device defect, an immediate health consequence that may result is prolonged hypoglycemia or hyperglycemia due to delay in treatment, as the blood glucose measurement is not available to guide treatment. In a worst-case situation, there is potential for battery swelling to result in explosion of the battery and/ or device. Exposure to explosion, and subsequently projectiles from the explosion, may result in several immediate health consequences, including concussion, headache, dizziness, eye irritation, blurred vision, eye injury, and vision impairment.