The Recall Desk

Hazard

Burn Injury recalls

2,084 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,084
Critical
32
Severe
734
Most recent
2026-09-10

Of the 2,084 burn injury recalls we have scored against our rubric, 32 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 734 (35%) 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 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.

601–625 of 2084

  • HighNHTSA·18V882000·2018-12-12

    Van Hool Recalls 2015-2018 Buses Due to Fire Extinguisher Defect

    Van Hool is recalling 2015-2018 TD925 and TDX25 buses because the fire suppression system actuator may fail to discharge during a fire.

    Product
    VAN HOOL — VAN HOOL TD925, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V827000·2018-11-22

    New Flyer Bus Recall for Fire Extinguisher Actuator Defect

    New Flyer is recalling certain 2013-2017 buses because a fire extinguisher actuator may fail, preventing the suppression system from discharging during a fire.

    Product
    NEW FLYER — NEW FLYER XN60, XN40, XD40, XDE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19714·2018-11-08

    Honda Recalls Pioneer 1000 Vehicles Due to Fire and Burn Hazards

    Honda is recalling approximately 56,000 Pioneer 1000 recreational off-highway vehicles because an incorrectly installed throttle body can ignite, posing fire and burn hazards.

    Product
    Recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19713·2018-11-07

    Kubota Recalls Mowers and Tractors Due to Coolant Burn Hazard

    Kubota is recalling about 121,100 mowers and compact tractors because hot coolant can spray out, posing a burn hazard. Three burn injuries have been reported.

    Product
    Kubota zero turn mowers, compact tractors, and ride-on mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0236-2019·2018-10-31

    GE Medical Systems Recalls Signa Architect MRI Scanners Due to Burn Risk

    GE Medical Systems is recalling four Signa Architect MRI scanners because a small area on the bore surface can get warm enough to cause a serious burn if proper padding is not used.

    Product
    SIGNA Architect system Product Usage: The Signa Architect system is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0202-2019·2018-10-31

    Boston Scientific Recalls Maestro 4000 Cardiac Ablation Systems Due to RF Energy Issue

    Boston Scientific is recalling Maestro 4000 Cardiac Ablation Systems because radiofrequency energy may continue to deliver after the foot switch is released.

    Product
    Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0, M0044000H0,M0044000R0, M0044000Z0,
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-0206-2019·2018-10-31

    ESAOTE MyLab Seven Ultrasound System Recalled for Probe Overheating Risk

    ESAOTE is recalling 10 MyLab Seven ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.

    Product
    MyLab Seven, Model 6400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0205-2019·2018-10-31

    ESAOTE MyLab Gamma Ultrasound System Recalled for Probe Overheating Risk

    ESAOTE S.P.A. is recalling 10 MyLab Gamma, Model 7410 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.

    Product
    MyLab Gamma, Model 7410
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2019·2018-10-31

    ESAOTE MyLab Alpha Ultrasound System Recalled for Probe Overheating Risk

    ESAOTE S.P.A. is recalling 10 MyLab Alpha Model 7400 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.

    Product
    MyLab Alpha, Model 7400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3279-2018·2018-10-03

    GE Medical Systems Recalls Discovery MR750w MRI Systems Due to Burn Risk

    GE Medical Systems is recalling 516 Discovery MR750w MRI systems because a small area on the bore surface can become warm enough to cause a serious burn if a patient touches it without proper padding.

    Product
    Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product Name (Model Number): A. 3.0T MR750 32CH (911000-3); B. 3.0T MR750W (5911000-3, 5481490-2, 5499460-7, 5499460-10, 5373011-3, 5352293, 5911000-3); C. 3.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18231·2018-09-25

    Provata Recalls Activity Trackers Due to Burn Hazard

    Provata Health is recalling about 30,000 promotional activity trackers because they can overheat and cause burns. Consumers should stop using the devices and contact the company for a free replacement.

    Product
    Provata activity trackers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18218·2018-09-11

    BlueStar and Big Chill Gas Ranges Recalled for Burn Hazard

    Prizer-Painter Stove Works is recalling BlueStar and Big Chill gas ranges and wall ovens because the convection fan can cause gas ignition and burns.

    Product
    BlueStar and Big Chill gas ranges and wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2893-2018·2018-08-29

    Philips SureSigns VS3 Vital Signs Monitor Recall for Battery Fire Risk

    Philips is recalling SureSigns VS3 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing fire and injury risks.

    Product
    Philips SureSigns VS3 Vital Signs Monitor, 863069 863070 863071 863072 863073 863074 The SureSigns VS3 monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2896-2018·2018-08-29

    Philips SureSigns VS2 Monitor Recall for Battery Overheating and Ignition Risk

    Philips is recalling SureSigns VS2 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing fire and injury risks.

    Product
    Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2 vital signs monitor is for use by healthcare professionals whenever there is a need for monitoring the physiological parameter of patients. Standard and optional parameters includ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2895-2018·2018-08-29

    Philips SureSigns Patient Monitors Recalled for Battery Overheating and Ignition Risk

    Philips is recalling SureSigns VM, VS, and VSV patient monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing injury and property damage risks.

    Product
    Philips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 863077 863085 863086 863317 863287 863288 863289 The SureSigns VM4, VM6, and VM8 patient monitors are for use by health care professionals whenever there is a need for monitoring the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2892-2018·2018-08-29

    Philips SureSigns VSV Monitors Recalled for Battery Overheating and Ignition Risk

    Philips is recalling SureSigns VSV monitors because lithium-ion batteries may overheat or ignite if not replaced on schedule, posing fire and injury risks.

    Product
    Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple adult, pediatric and neonatal patients, and where the clinician decides to monitor cardiac arrhythmia of adult, pediatric and neonatal patients to gain information for the treatment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2894-2018·2018-08-29

    Philips SureSigns VS4 Vital Signs Monitor Recalled for Battery Fire Risk

    Philips is recalling SureSigns VS4 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing injury and property damage risks.

    Product
    Philips SureSigns VS4 Vital Signs Monitor, 863283 863286 The SureSigns VS4 vital signs monitor is for use by healthcare professionals whenever there is a need for monitoring the physiological parameters of patients. The SureSigns VS4 monitor is for monitoring, recording, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·18199·2018-08-22

    Vornado VH101 Electric Space Heaters Recalled Due to Fire and Death

    Vornado Air is recalling VH101 Personal Vortex electric space heaters because they can overheat, posing fire and burn hazards. One death and 19 fire reports have been linked to the units.

    Product
    VH101 Personal Vortex electric space heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2792-2018·2018-08-22

    MegaPower Electrosurgical Generator Recalled for Potential Patient Burns

    Megadyne Medical Products is recalling 8,380 MegaPower Electrosurgical Generators because plugging two devices into the same port can activate both, potentially causing patient burns.

    Product
    MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
    Category
    Medical Device
    Distribution
    Distributed nationwide