The Recall Desk

Hazard

Thermal Burn recalls

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

What the numbers show

Total
18
Critical
0
Severe
5
Most recent
2024-07-17

Of the 18 thermal burn recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (28%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all thermal burn 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.

1–18 of 18

  • SevereFDA (Devices)·Z-2315-2024·2024-07-17

    Baxter iLED 7 surgical lights recalled due to thermal burn risk

    Baxter Healthcare is recalling iLED 7 surgical lights due to customer reports of thermal skin injuries. The recall affects approximately 6,243 units distributed worldwide.

    Product
    iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo Surgical Lights); e) 4068310 (Ceiling Trio Surgical Lights); f) 4068410 (Ceiling…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2313-2024·2024-07-17

    Baxter VidiaPort and Trulight surgical lights recalled for thermal burn risk

    Baxter Healthcare Corporation is recalling VidiaPort and Trulight surgical light systems due to customer reports of thermal skin injuries. Approximately 275 units were distributed worldwide.

    Product
    VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical Lights)
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·23140·2023-03-02

    RELiON InSight Series Lithium Batteries Recalled for Thermal Burn and Fire Risk

    RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.

    Product
    RELiON InSight Series® lithium batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23068·2022-12-15

    Jacuzzi and Sundance Hot Tubs Recalled for Thermal Burn Hazards

    Sundance Spas is recalling certain Jacuzzi and Sundance brand hot tubs because the temperature sensor may relay incorrect water temperatures, causing water hotter than the set temperature and posing burn and heat stroke hazards. No injuries have been reported.

    Product
    Jacuzzi® Hot Tubs and Sundance® Spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22159·2022-06-16

    Schneider Electric Electrical Panels Recalled for Fire and Burn Hazards

    Schneider Electric is recalling about 1.4 million Square D QO Plug-on-Neutral Load Centers because they can overheat, creating thermal burn and fire hazards. The company is contacting purchasers and installers to arrange free inspections and repairs.

    Product
    Square™ D QO™ Plug-on-Neutral Load Centers, also known as, Load Centers, Breaker Boxes, Electrical Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2240-2021·2021-08-18

    Covidien Sonicision Surgical Generator Recalled for Manufacturing Defect Risk

    Covidien recalls 96 units of its Sonicision Reusable Generator surgical device due to a manufacturing assembly error that may cause device malfunction, thermal burns, or tissue damage. The defect may also disable the audio indicator that signals device activation.

    Product
    Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive the active blade. Product Number: SCGAA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V667000·2020-10-29

    Jayco and Entegra motorhomes recalled for insufficient engine cover insulation

    Jayco, Inc. is recalling certain 2020-2021 motorhomes due to engine covers with insufficient heat insulation. This may cause excessive interior surface temperatures that increase the risk of injury to occupants.

    Product
    ENTEGRA — ENTEGRA, JAYCO VISION XL, VISION, EMBLEM, ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1872-2019·2019-07-03

    Thermo Scientific General Purpose Dynamic Bath Recalled for Assembly Error

    Thermo Fisher Scientific is recalling three General Purpose Dynamic Bath units due to an assembly error that may cause the fluid temperature to rise above the user's set point.

    Product
    Thermo Scientific General Purpose Dynamic Bath Precision 28L GP Bath Model Number: TSGP28
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·18172·2018-06-05

    Keyera Energy Recalls Propane Gas Due to Fire and Explosion Hazards

    Keyera Energy is recalling under-odorized propane gas in Texas and Louisiana due to fire and explosion risks. Consumers should contact suppliers for a free inspection.

    Product
    Propane (LP) gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·07130·2007-03-15

    Amprobe Recalls Digital Clamp Meters Due to Shock Hazard

    Amprobe is recalling about 70,000 digital clamp meters because they may display incorrect voltage readings, posing a risk of shock or electrocution.

    Product
    Amprobe Digital Clamp Meters used for electrical testing
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·02253·2002-09-19

    Nikon Recalls Coolpix 2000 Digital Cameras Due to Thermal Burn Hazard

    Nikon is recalling approximately 9,100 Coolpix 2000 digital cameras because a short circuit in the battery compartment can cause thermal burns. Consumers should remove batteries and contact Nikon for a free replacement.

    Product
    2000-Model Digital Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·02512·2001-12-17

    Next Level Communications Recalls PowDec Power Supplies for Computer Modems

    Next Level Communications is recalling PowDec power supplies for computer modems because an internal component can overheat and melt the plastic housing, posing a thermal burn hazard.

    Product
    Power Supplies used with Next Level ADSL/VDSL ETHERset (modem) units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·01061·2000-12-22

    Propane Gas Recalled for Insufficient Odorant Levels

    Cenex Harvest States Cooperatives is recalling propane gas distributed since June 1, 2000, because it may lack sufficient odorant to detect leaks, posing fire and explosion risks.

    Product
    Propane gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide