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.

251–275 of 742

  • HighFDA (Devices)·Z-1870-2019·2019-07-03

    Thermo Scientific General Purpose Dynamic Bath Recalled for Assembly Error

    Thermo Fisher Scientific is recalling four units of the General Purpose Dynamic Bath 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 2L-Shallow GP Bath Model Number: TSGP2S
    Category
    Medical Device
    Distribution
    4 states
  • SevereCPSC·19115·2019-05-02

    Excalibur EZ DRY Food Dehydrators Recalled Due to Fire Hazard

    Greenfield World Trade is recalling Excalibur EZ DRY food dehydrators because they can overheat, posing a fire hazard and causing minor burn injuries.

    Product
    Excalibur EZ DRY food dehydrators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·19107·2019-04-18

    Tekno Recalls Tuff Smoke-Less Grills Due to Fire and Burn Hazards

    Tekno Products is recalling Tuff smoke-less grills because they can overheat, posing fire and burn hazards. Consumers should stop using the grills and return them for a refund.

    Product
    Tuff smoke-less grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1058-2019·2019-04-03

    Sunset Compressor Nebulizer Recalled for Overheating and Mouthpiece Detachment Risk

    SANRAI INTERNATIONAL LLC is recalling 150 Sunset Compressor Nebulizer units in South Africa due to voltage incompatibility risks.

    Product
    Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-powered air nebulizer compressor system intended to provide a source of compressed air for medical purposes for use in home healthcare. It is to be used with a nebulizer kit to pro
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·19098·2019-04-03

    Matco Tools Wireless Chargers Recalled Due to Burn Hazard

    Professional Tool Products is recalling Matco Tools wireless chargers because they can overheat and cause burns. Consumers should stop using them and return them for a refund.

    Product
    Matco Tools wireless chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19096·2019-04-02

    Spector & Co. Recalls T119 Elf Power Bank Chargers Due to Fire Hazard

    Spector & Co. is recalling T119 Elf power bank chargers because they can overheat and pose a fire hazard. No injuries or property damage have been reported.

    Product
    T119 Elf power bank chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·19090·2019-03-26

    Universal Rechargeable Power Banks Recalled Due to Fire Hazard

    Daniel M. Friedman & Associates is recalling about 170,500 universal rechargeable power banks due to a fire hazard. The devices can overheat, causing property damage.

    Product
    Universal rechargeable power banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0854-2019·2019-02-27

    Philips PageWriter TC50 ECG Devices Recalled for Overheating and Fire Risk

    Philips is recalling PageWriter TC50 electrocardiogram devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0856-2019·2019-02-27

    Philips PageWriter TC20 Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC20 devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury.

    Product
    PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0855-2019·2019-02-27

    Philips PageWriter TC30 ECG Devices Recalled for Overheating and Ignition Risk

    Philips is recalling PageWriter TC30 ECG devices because end-of-life batteries may overheat, melt the case, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0825-2019·2019-02-20

    Hemotherm CE Dual Reservoir Cooler/Heater Recalled for Overheating Risk

    Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.

    Product
    Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir Cooler/Heater is used to lower, maintain, or raise the temperature of the water flowing through a Blood Oxygenator / Heat Exchanger that is used to cool or warm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0788-2019·2019-02-06

    GE Healthcare Recalls LOGIQ P6 Ultrasound Scanners Due to Probe Heating

    GE Healthcare is recalling 1,897 LOGIQ P6 ultrasound scanners (Models BT07 and BT09) because the probe-head surface can reach increased temperatures during specific scans.

    Product
    GE HEALTHCARE LOGIQ P6 Premium TruScan(TM) Imagining Technology: (a) Model BT09 (b) Model BT07 Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cepha
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0791-2019·2019-02-06

    3M Surgical Clipper Recalled for Overheating Risk During Charging

    3M is recalling 19,860 Surgical Clippers due to reports of overheating when charging from modified sine wave power inverters in mobile EMS settings.

    Product
    3M(TM) Surgical Clipper by Remington(R) REF 9602 The 3M Surgical Clipper Classic, 9602, is intended to remove body hair and head hair from patients in preparation for any medical procedure requiring hair removal.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0588-2019·2018-12-19

    GE LOGIQ E10 Ultrasound System Recalled for Potential Burn Injury

    GE Healthcare is recalling 103 LOGIQ E10 Ultrasound Systems because a trans-esophageal probe may overheat, posing a risk of burn injury to patients.

    Product
    GE LOGIQ E10 Ultrasound System, Model #530000E10. The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/Obstetrics; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0558-2019·2018-12-12

    Siemens Artis Zee and Zeego X-ray Systems Recalled for Cooling Hose Leak

    Siemens is recalling 64 Artis Zee and Zeego angiography systems due to a possible cooling hose leak that can cause the X-ray tube to overheat and block imaging.

    Product
    Artis Zee and Zeego, model no. 10272462 AXIOM Artis zee/Zeego is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    12 states
  • SevereNHTSA·18V843000·2018-11-28

    Keystone RV Recalls 2019 Travel Trailers Due to Axle Hub Bearing Defect

    Keystone RV Company is recalling certain 2019 recreational trailers because the inner axle hub bearings may not have been sufficiently greased, which could cause overheating, hub failure, and increased crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN OUTBACK, BULLET, AEROLITE, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19036·2018-11-20

    Seabreeze Recalls Smart Thermaflo Bathroom Heater Fans Due to Fire Hazard

    Seabreeze International is recalling Smart Thermaflo Bathroom Heater Fans because the safety cutoff can fail, allowing the unit to overheat and catch fire.

    Product
    Smart Thermaflo Bathroom Heater Fans with nightlight
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0281-2019·2018-11-07

    Leica BOND Slide Labeler Printers Recalled for Fire Hazard

    Leica Microsystems is recalling BOND Slide Labeler Zebra Printers because the power supply unit may overheat or cause a fire due to an improperly-mixed phosphorus compound.

    Product
    BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301, for use with BOND-III and BOND-MAX instruments
    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
  • HighFDA (Devices)·Z-0201-2019·2018-10-31

    GE Healthcare Recalls 3.0T MR750 MRI Scanners Due to Coil Overheating Risk

    GE Medical Systems is recalling 356 Discovery 3.0T MR750 MRI scanners because a specific coil can overheat in Mode 2, posing a risk of serious patient thermal injury.

    Product
    GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2.
    Category
    Medical Device
    Distribution
    26 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