The Recall Desk

Hazard

Overheating recalls

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

What the numbers show

Total
742
Critical
7
Severe
282
Most recent
2026-08-26

Of the 742 overheating recalls we have scored against our rubric, 7 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 282 (38%) 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 overheating 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.

276–300 of 742

  • 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-0178-2019·2018-10-24

    Siemens Biograph mCT PET/CT Scanners Recalled for Plug Overheating Risk

    Siemens Medical Solutions is recalling 890 Biograph mCT PET/CT scanners because plug terminals may become loose and overheat.

    Product
    Biograph mCT: a) S(64)-3R, Material Number 10248669 b) S (20) -3R, Material Number 10507786 c) Flow 20-4R, Material Number 10528958 d) m Flow 64-4R, Material Number 10529161 e) mCT S(40)-4R, Material Number 10248671 f) mCT S(64)-4R, Material Number 0248672 g) mCT S(20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0177-2019·2018-10-24

    Siemens Biograph Horizon PET/CT Scanners Recalled for Plug Overheating Risk

    Siemens Medical Solutions is recalling 78 Biograph Horizon PET/CT scanners because loose plug terminals may overheat.

    Product
    Biograph Horizon a) 3R, Material Number 10532746 b) 4R, Material Number 10532748 The Siemens Biograph Horizon and Biograph mCT systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high res
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V732000·2018-10-17

    BMW Recalls 2019 X5 xDrive40i Vehicles for Fire Risk

    BMW is recalling 2019 X5 xDrive40i vehicles because a short circuit in the Body Domain Controller may cause overheating and increase the risk of a fire.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19009·2018-10-11

    Cooper Lighting Recalls Solar-Powered Outdoor LED Fixtures Due to Fire Hazard

    Cooper Lighting is recalling specific All-Pro and Defiant solar-powered outdoor LED light fixtures because the batteries can overheat and cause a fire.

    Product
    All-Pro and Defiant solar-powered outdoor LED light fixtures
    Category
    Consumer Product
    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
  • SevereNHTSA·18V658000·2018-09-24

    Grand Design Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Grand Design is recalling 2019 Reflection, Imagine, and Transcend travel trailers because missing inner axle bearings may cause overheating and fire.

    Product
    GRAND DESIGN — GRAND DESIGN TRANSCEND, REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V595000·2018-09-07

    GM Recalls 2014-2016 Cadillac CTS for Seat Heater Fire Risk

    General Motors is recalling 2014-2016 Cadillac CTS vehicles because damaged front seat heaters may overheat and cause a fire when the car is remotely started.

    Product
    CADILLAC — CADILLAC CTS
    Category
    Vehicle
    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
  • HighFDA (Devices)·Z-2570-2018·2018-08-08

    XLTEK EMU40EX EEG Headbox Recalled for Component Degradation

    Natus Neurology is recalling 462 XLTEK EMU40EX EEG Headboxes because an internal electronic component may degrade, causing the unit to overheat and the plastic case to melt.

    Product
    XLTEK EMU40EX EEG Headbox
    Category
    Medical Device
    Distribution
    34 states
  • SevereCPSC·18186·2018-08-02

    Zebra Thermal Printer Power Supply Units Recalled for Fire Hazard

    Zebra Technologies is expanding a recall of power supply units for thermal printers due to a fire hazard. The units can overheat and catch fire when exposed to moisture.

    Product
    Power supply units for Zebra brand thermal printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2536-2018·2018-08-01

    Bard Medical Recalls Arctic Sun Temperature Management Systems Due to Wiring Defect

    Bard Medical Division is recalling 5,608 Arctic Sun 5000 Temperature Management Systems because an improper wiring connection may cause overheating and component failure.

    Product
    Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating system, indicated for monitoring and controlling patient temperature within a range of 32¿C to 38.5¿C (89.6¿F to 101.3¿F) in adult and pediatric patients of
    Category
    Medical Device
    Distribution
    52 states
  • HighCPSC·18195·2018-07-27

    Hirsch Gift Recalls CloudCharge Wireless Charging Pads Due to Burn Hazard

    Hirsch Gift is recalling about 21,000 CloudCharge Qi Wireless Charging Pads because they can overheat and cause burns. Consumers should stop using the pads and contact the company for a free replacement.

    Product
    CloudCharge Qi Wireless Charging Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18746·2018-06-06

    Vernier Circuit Board 2 Recalled Due to Burn Hazard

    Vernier Software & Technology is recalling Circuit Board 2 units because overheating switches can cause burns. About 4,200 units were sold between 2015 and 2018.

    Product
    Vernier Circuit Board 2
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V229000·2018-04-11

    Audi Recalls 2012-2017 Models Due to Coolant Pump Fire Risk

    Volkswagen Group of America is recalling specific Audi models because a coolant pump defect may cause overheating or short-circuiting, increasing the risk of a fire.

    Product
    AUDI — AUDI A6, A5, Q5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1295-2018·2018-04-11

    Magellan LeadCare II Blood Lead Analyzer Recalled for Battery Overheating Risk

    Magellan Diagnostics is recalling LeadCare II Blood Lead Analyzers because incorrect battery placement may cause overheating and potential finger burns.

    Product
    LeadCare II Blood Lead Analyzer Part Numbers: 70-6760, 70-6529-R, 70-6760-P, 70-6760-R. Intended for in vitro (external) use only.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1296-2018·2018-04-11

    Magellan LeadCare Plus Blood Lead Analyzer Recalled for Battery Overheating Risk

    Magellan Diagnostics is recalling 79 LeadCare Plus Blood Lead Analyzers because incorrect battery placement may cause overheating and potential finger burns.

    Product
    LeadCare Plus Blood Lead Analyzer Part Number: 82-0001 Intended for the quantitative measurement of lead in a whole blood sample.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·18135·2018-04-03

    3M Recalls Scotch Thermal Laminators Due to Overheating Burn Hazard

    3M is recalling about 395,000 Scotch thermal laminators because the plastic enclosure can overheat, posing a burn hazard. No injuries have been reported.

    Product
    Scotch™ thermal laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1138-2018·2018-03-28

    ESAOTE MyLab Ultrasound Systems Recalled for Probe Overheating Risk

    ESAOTE is recalling specific MyLab Ultrasound Systems because the probe head may overheat during use in certain settings.

    Product
    MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; Probes: BL433, C 18, CA541, EC1123, EC123, IH 618, IOT332, IOT342, L 415, LA332E, LA435, LA523, LA533, SI2C41, SL2325, TRT33
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1137-2018·2018-03-28

    ESAOTE MyLab Ultrasound Systems Recalled for Probe Overheating Risk

    ESAOTE is recalling specific MyLab Ultrasound Systems because the probe head may overheat in certain settings.

    Product
    MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10
    Category
    Medical Device
    Distribution
    5 states
  • HighCPSC·18730·2018-03-15

    eheat Recalls Envi Wall Heaters Due to Overheating and Burn Hazard

    eheat is recalling about 35,000 Envi wall heaters sold in the U.S. and Canada due to a defect that can cause overheating, smoke, or melting, posing a burn hazard.

    Product
    Envi high-efficiency electric panel heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18E014000·2018-03-08

    ATC Recalls 7-Way Wiring Harnesses for Truck Caps Due to Fire Risk

    American Technology Components is recalling specific 7-Way Wiring Harnesses used for aftermarket truck cap installations because the wiring may overheat, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0719-2018·2018-03-07

    Medistim Veriq System Recalled Due to Component Overheating and Smoke Emission

    Medistim Asa is recalling two Medistim Veriq System units because a component overheated, causing connector melting and smoke emission.

    Product
    MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0716-2018·2018-03-07

    Philips Recalls Allura Xper Systems Due to Anode Drive Unit Failure

    Philips is recalling 705 Allura Xper systems because Anode Drive Units may fail in high-voltage regions, reducing X-ray performance to emergency mode.

    Product
    Allura Xper systems with Certeray X-ray Generator located in regions with high mains (480V) voltage. Product Usage: The Allura Xper series is intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide