The Recall Desk

Hazard

Burn Injury recalls

477 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all burn injury recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

101–125 of 477

  • HighCPSC·25419·2025-07-31

    Baby Loren Children's Loungewear Recalled for Flammability Standards Violation

    About 340 Baby Loren Morning children's cotton dresses sold from October 2022 through March 2025 violate federal flammability standards for sleepwear, creating a risk of burns and death. No injuries have been reported.

    Product
    Baby Loren Morning Dresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25403·2025-07-24

    FENGQS F7 Pro E-bikes Recalled Due to Battery Fire and Burn Hazards

    FENGQS F7 Pro e-bikes are being recalled because their lithium-ion batteries can overheat and ignite, creating fire and burn hazards. FENGQS has received 13 reports of ignition incidents, with 2 resulting in fires and $4,000 in property damage.

    Product
    FENGQS F7 Pro E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25395·2025-07-24

    Frigidaire Minifridges Recalled for Fire and Burn Hazard

    About 634,000 Frigidaire minifridges may catch fire due to internal electrical short circuits. At least 26 incidents causing property damage exceeding $700,000 have been reported, including two smoke inhalation injuries.

    Product
    Frigidaire-brand Minifridges, models EFMIS129, EFMIS137, EFMIS149 and EFMIS175, limited to the listed serial numbers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25389·2025-07-17

    CasaClean Handheld Steamers Recalled Due to Serious Burn Injury Risk

    Deale International is recalling about 23,000 CasaClean Handheld Steamers that can leak steam or spew hot water, causing serious burns. The company has received 26 reports of leaks, including 13 consumers with burns.

    Product
    CasaClean Handheld Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25392·2025-07-17

    Babyletto Kiwi Electronic Recliners with USB Port Recalled for Overheating

    Babyletto Kiwi Electronic Recliners with USB charging ports are recalled for overheating and sparking in the USB module. About 9,030 units are affected; consumers should stop use immediately and contact Babyletto for a free repair kit.

    Product
    Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V454000·2025-07-07

    2020-2025 Land Rover Range Rover Evoque Passenger Air Bag May Tear

    Jaguar Land Rover is recalling 2020-2025 Range Rover Evoque vehicles because the passenger air bag may tear during deployment, reducing crash protection and potentially causing burn injuries.

    Product
    LAND ROVER — 2021 LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1904-2025·2025-07-02

    Broselow Pediatric Emergency Tape recalled for incorrect dosing information

    SunMed's Broselow pediatric emergency tape has incorrect dosing information printed in critical zones. Using these incorrect values could cause cardiac arrest, burns, and serious electrolyte imbalances during emergency care.

    Product
    Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2025·2025-06-25

    UROSKOP Omnia Medical Imaging Device Recalled for Fire Hazard

    Siemens Medical Solutions is recalling 95 units of the UROSKOP Omnia medical imaging device nationwide due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. No injuries have been reported.

    Product
    UROSKOP Omnia. Model Number: 10094910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1930-2025·2025-06-18

    Philips MRI System Gradient Coil Component May Overheat and Ignite Smoke or Fire

    Philips has recalled 16 Intera 1.5T Achieva Nova MRI systems due to a gradient coil component that may overheat and produce smoke or fire, risking patient and operator injury.

    Product
    Intera 1.5T Achieva Nova Product Number: 781172;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25342·2025-06-18

    AstroAI minifridges recalled due to fire and burn hazards

    AstroAI is recalling about 249,100 minifridges with a defective electrical switch that can catch fire. The CPSC received 70+ reports of fires, with two incidents causing $360,000 in property damage.

    Product
    4 Liter/6 Can Minifridges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1921-2025·2025-06-18

    SOLTIVE Laser System Recalled for Potential Thermal Incident Risk

    Olympus is recalling 1,549 SOLTIVE surgical laser systems due to potential thermal incidents—including smoke, sparks, burning, or unsteady flames—caused by fiber fracturing during clinical use.

    Product
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1932-2025·2025-06-18

    Philips MRI System Recall Due to Potential Fire and Smoke Risk

    Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a potential component failure in the gradient coil that could generate heat, smoke, and fire, creating risks of burns, smoke inhalation, and asphyxiation.

    Product
    Intera 1.5T Explorer/Nova Dual Product Number: 781108;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1936-2025·2025-06-18

    Philips SmartPath dStream Gradient Coil Fire Risk Recall

    Philips is recalling the SmartPath dStream for 1.5T due to potential fire and smoke hazard in the gradient coil component. Users face risks of smoke inhalation, burns, and asphyxiation.

    Product
    SmartPath to dStream for 1.5T¿; Product Number: 782146;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1935-2025·2025-06-18

    Philips Intera Achieva 1.5T MRI systems recalled for potential gradient coil fire

    Philips is recalling Intera Achieva 1.5T Pulsar MRI systems due to a gradient coil component defect that can produce smoke and fire. Potential hazards include burns, smoke inhalation, and asphyxiation.

    Product
    Intera Achieva 1.5T Pulsar; Product Number: 781171;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1934-2025·2025-06-18

    MRI System Gradient Coil Component Failure Poses Fire and Smoke Risk

    Philips Intera 1.5T MRI systems may experience gradient coil component failure that can produce smoke or fire, posing risks of burns, inhalation injury, and asphyxia to patients and operators.

    Product
    Intera 1.5T Omni/Stellar; Product Number: 781104;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1933-2025·2025-06-18

    Philips Intera 1.5T MRI Systems Gradient Coil Fire Risk Recall

    Philips is recalling two Intera 1.5T Master/Nova MRI systems due to a potential gradient coil component failure that could overheat and produce smoke or fire, risking inhalation injuries, burns, and asphyxia.

    Product
    Intera 1.5T Master/Nova Product Number: 781106;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1931-2025·2025-06-18

    Philips 1.5T MRI System Gradient Coil May Overheat and Produce Smoke or Fire

    Philips is recalling Intera 1.5T MRI systems because a Gradient Coil component failure can cause the system to overheat and produce smoke or fire, risking inhalation injury, burns, and asphyxia.

    Product
    Intera 1.5T Achieva Nova-Dual Product Number: 781173;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1962-2025·2025-06-18

    Rechargeable Batteries for Hillrom WELCH ALLYN PocketScope Handle Recalled for Burn Risk

    Baxter Healthcare is recalling 277 rechargeable batteries used in Hillrom WELCH ALLYN PocketScope handles because they can short circuit and overheat, creating a risk of user burns. The affected lot is 25-043 with expiration August 2027.

    Product
    2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1920-2025·2025-06-18

    Surgical laser system recalled for potential thermal incidents during use

    Olympus SOLTIVE Pro SuperPulsed Laser System recalled due to potential thermal incidents (smoke, sparks, burning, flames) caused by fiber fracturing during clinical use. Affects 201 units worldwide.

    Product
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Number: TFL-SLS, TFL-SLS-JA (Japan only); Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and flexibility to ureteroscopy,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1922-2025·2025-06-18

    Soltive SuperPulsed Laser Fibers Recalled for Thermal Incident Risk

    Olympus is recalling Soltive SuperPulsed Laser Fibers due to potential thermal incidents including smoke, sparks, burning, and flames during surgical use, caused by fiber fracturing. No injuries have been reported.

    Product
    Brand Name: Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser Fibers - Single Use Model/Catalog Numbers: TFL-FBX150BS, TFL-FBX200BS, TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFL-FBX550S, TLF-FBX940S, TFL-FBX150BS-JA (Japan Only), TFL-FBX550S-JA (Japan Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1966-2025·2025-06-18

    Allon 2001 heating device may exceed safe temperature without alarming user

    Allon 2001 devices can heat water beyond safe limits when sensors are disconnected and alarms are disabled, risking patient burns without warning. 229 units are affected worldwide.

    Product
    Allon 2001. Part Number: 200-00263
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25338·2025-06-12

    Anker PowerCore 10000 Power Banks Recalled for Fire and Burn Hazards

    About 1.16 million Anker PowerCore 10000 power banks (model A1263) are recalled due to lithium-ion battery overheating. The company received 19 reports of fires, explosions, two minor burns, and $60,700 in property damage.

    Product
    Anker PowerCore 10000 power banks (model A1263 only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide