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.

451–475 of 742

  • SevereNHTSA·14E055000·2014-08-20

    Thermo King Inverters Recalled for Fire Risk in Tractor Cabins

    Thermo King is recalling specific 1100W, 1500W, and 2000W inverters sold between May and July 2014 because they may spark or overheat, posing a fire hazard.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1994-2014·2014-07-16

    Intuitive Surgical Recalls Patient Side Cart Battery Boxes for Overheating Risk

    Intuitive Surgical is recalling 2,606 Patient Side Cart Battery Boxes used with the da Vinci A surgical system because they may overheat and bulge during charging.

    Product
    Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc. Sunnyvale, CA 94086
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2039-2014·2014-07-16

    Karl Storz Recalls Essential NEO Audio/Visual Units Due to Overheating Cable

    Karl Storz Endoscopy is recalling 968 Essential NEO audio/visual integration units because the connected power cable could overheat, generate smoke, and cause the peripheral to stop working.

    Product
    Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14228·2014-07-10

    Gemini Recalls Power Adaptor Chargers Due to Burn Hazard

    Gemini is recalling about 31,000 promotional power adaptors/chargers because they can overheat and cause burns. Consumers should stop using and dispose of the units.

    Product
    Power adaptor/chargers (promotional giveaway)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1940-2014·2014-07-09

    Global Cooling Stirling Ultracold Portable Shuttle Recalled for Overheating

    Global Cooling Inc is recalling 413 Stirling Ultracold Portable Shuttle units because the external power supply input overheats at the connection to the freezer.

    Product
    Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and storage and transport of biological specimens.
    Category
    Medical Device
    Distribution
    39 states
  • SevereCPSC·14195·2014-05-29

    Sunbeam Recalls Holmes Ceramic Heaters Due to Fire Hazard

    Sunbeam is recalling about 151,600 Holmes ceramic heaters because they can overheat and pose a fire hazard. Consumers should stop using the units and contact Sunbeam for a refund.

    Product
    Holmes Ceramic Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1628-2014·2014-05-28

    Philips Recalls Lithium Ion Batteries for IntelliVue Patient Monitors

    Philips Medical Systems is recalling specific lithium ion batteries for IntelliVue Patient Monitors because they may overheat, ignite, or explode after extended use.

    Product
    Lithium Ion Battery M4605A and M4607A for use with IntelliVue Patient Monitors. The monitor is used for monitoring and recording of, and to generate alarms for, multiple physiological parameters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1523-2014·2014-05-28

    Maquet Datascope Intra-Aortic Balloon Pump Recall for Fan Assembly Failure

    Maquet Datascope is recalling 11,881 Intra-Aortic Balloon Pump units worldwide due to a potential fan assembly failure that could cause the power supply to overheat and shut down without warning.

    Product
    Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate intra-aortic balloons in cardiovascular procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14176·2014-05-14

    Cabela's Recalls Electronic Jerky Blaster Due to Fire Hazard

    Cabela's is recalling Electronic Jerky Blasters because the battery charger adapter can overcharge, causing the battery and adapter to overheat.

    Product
    Electronic Jerky Blaster
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1480-2014·2014-04-30

    GE Healthcare Recalls MR Scanners Due to Gradient Coil Overheating Risk

    GE Healthcare is recalling 1,546 MRI scanners worldwide because gradient coil connections may loosen, causing overheating, smoke, and potential fire.

    Product
    GE Healthcare, Discovery MR450, Discovery MR750, Optima MR450w, Optima MR 450w GEM, Discovery MR750w, and Discovery MR750w GEM products. Magnetic Resonance Diagnostic Device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1488-2014·2014-04-30

    GE Vivid E9 Ultrasound System Recalled for Probe Overheating Risk

    GE Healthcare is recalling Vivid E9 Ultrasound Systems because incorrect power settings for four specific probe types may cause them to overheat.

    Product
    GE Vivid E9 Ultrasound System, a general-purpose ultrasound system, specialized for use in cardiac imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·14162·2014-04-29

    DGL Group Recalls Vibe USB Mobile Power Bars Due to Fire Hazard

    DGL Group is recalling Vibe USB Mobile Power Bars sold at Five Below because they can overheat and cause fires. No injuries have been reported, but minor property damage has occurred.

    Product
    Vibe USB Mobile Power Bar
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14156·2014-04-23

    Summer Infant Video Monitor Batteries Recalled for Overheating and Burn Hazard

    Summer Infant is recalling rechargeable batteries in video monitors due to overheating and rupture risks. Consumers should remove the battery and contact the company for a replacement.

    Product
    Rechargeable batteries used in Summer Infant video monitors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2014·2014-04-09

    Siemens ACUSON P300 Ultrasound Systems Recalled for Transducer Overheating

    Siemens is recalling ACUSON P300 ultrasound systems with PA230 transducers because they may exceed maximum allowable surface temperature limits.

    Product
    Siemens Medical Solutions, ACUSON P300 Ultrasound system with P300 PA 230E cardiac probe (Esaote product 7348). Provides imaging for guidance of biopsy and imaging to assist in the placement of needles in vascular or other anatomical structures as well as peripheral nerve
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·14723·2014-03-14

    MobilePower Instant Boost 500 Power Packs Recalled for Fire Hazard

    MobilePower is recalling about 9,800 Instant Boost 500 power packs sold by QVC because they can overheat and cause fires. No injuries have been reported.

    Product
    MobilePower Instant Boost 500 power packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14120·2014-03-05

    Twin-Star Recalls Duraflame Electric Space Heaters Due to Fire and Burn Hazards

    Twin-Star is recalling about 31,000 Duraflame electric space heaters because they can overheat, melt, and catch fire. Consumers should unplug the units and contact the company for a refund.

    Product
    Duraflame electric space heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14115·2014-02-25

    BRP Recalls Ski-Doo and Can-Am Heated Gloves Due to Fire Hazard

    BRP is recalling Ski-Doo and Can-Am heated gloves and lithium-ion batteries because the battery packs can overheat and cause fires. No injuries were reported, but minor property damage occurred.

    Product
    Ski-Doo® and Can-Am® heated gloves and Lithium-Ion Rechargeable Batteries.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14095·2014-01-30

    Gree Recalls GE Brand Dehumidifiers Due to Fire and Burn Hazards

    Gree is expanding its recall to include GE-brand dehumidifiers that can overheat, smoke, and catch fire. Consumers should unplug the units and contact Gree for a refund.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0811-2014·2014-01-29

    Ziemer FEMTO LDV Z2, Z4, and Z6 Lasers Recalled for Monitor Overheating

    Ziemer USA Inc. is recalling five FEMTO LDV femtosecond surgical lasers because a controller board defect may cause the video monitor to overheat and shut off.

    Product
    1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an ophthalmic surgical laser indicated for use in the creation of corneal incisions in patients undergoing LASIK surgery or other treatment requiring lamellar resection of the cornea at constant depth relative to the corneal surfa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14087·2014-01-23

    Rayovac Flashlights Recalled by Spectrum Brands Due to Burn Hazard

    Spectrum Brands is recalling specific Rayovac LED flashlights because they can overheat and melt, posing a burn hazard. No injuries have been reported.

    Product
    Rayovac flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V007000·2014-01-13

    General Motors Recalls 2014-2015 Trucks and SUVs for Engine Fire Risk

    General Motors is recalling specific 2014-2015 Chevrolet, GMC, and Cadillac vehicles because overheated exhaust components may melt plastic parts and cause an engine fire.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO, SIERRA 1500, ESCALADE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide