Hazard

Overheating recalls

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

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.

101–125 of 163

HighFDA (Devices)·Z-2471-2024·2024-08-14
GE SIGNA 1.5T MR Systems May Overheat Implants in Low SAR Mode
GE Medical Systems recalled 2,146 SIGNA 1.5T MR systems that may overheat implants during certain imaging sequences in Low SAR mode due to a software defect in radiofrequency safety calculations.
Product
1.5T SIGNA HDxt Family, with affected software versions: HD16.0_V03 to HD16.4, HD23.0_V03, HD28.0, HD29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2482-2024·2024-08-14
MRI System Software Error Can Cause Implant Overheating in Low SAR Mode
GE HealthCare's Discovery MR950 MRI system may incorrectly calculate heating safety limits when using certain imaging sequences in Low SAR Mode, potentially causing overheating of MR-conditional implants.
Product
Discovery MR950, with affected software versions: 7T23.0; Nuclear Magnetic Resonance Imaging System - research use only
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2467-2024·2024-08-14
Discovery MR450 MRI System Can Overheat Implants Under Specific Conditions
GE Discovery MR450 MRI systems with certain software versions can cause implant overheating under specific scanning conditions. 23 units worldwide require firmware updates.
Product
Discovery MR450 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0; Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
0 states
HighNHTSA·24V557000·2024-07-26
BMW R 1300 GS starter motor relays may overheat
BMW is recalling certain 2024 R 1300 GS motorcycles because the starter motor relay housing may have been manufactured incorrectly, resulting in a damaged relay that can overheat.
Product
BMW — 2024 BMW R 1300 GS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2165-2024·2024-07-03
Philips SENSE XL Torso Coil 1.5T Recalled for Overheating Risk
Philips recalled 14 SENSE XL Torso Coils worldwide due to potential overheating. The coils could heat up during use and cause patient burn injuries.
Product
SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567502281, 453567502282, 453567502283, 453567502284, 453567502285, 453567502286, 459801585212.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2180-2024·2024-07-03
X-ray Table Touch Display Power Supply Fire Hazard
Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.
Product
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2188-2024·2024-07-03
Siemens AXIOM Vertix Solitaire Display Fire Risk from Power Supply Short Circuit
Siemens is recalling the AXIOM Vertix Solitaire diagnostic imaging component due to a short circuit in the Touch Display's power supply unit that may cause overheating and fire. Two units with serial numbers 1239 and 1241 are affected.
Product
ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2182-2024·2024-07-03
Radiographic X-ray Table Recalled Due to Fire Hazard in Power Supply
Siemens AXIOM MULTIX MP radiographic X-ray tables are being recalled due to a potential short circuit in the touch display's power supply unit that may cause overheating or fire. 12 units nationwide are affected.
Product
AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395381
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2184-2024·2024-07-03
Medical imaging system recalled for power supply fire risk
Siemens is recalling 2 AXIOM Vertix MD imaging systems nationwide due to a potential fire hazard from a short circuit in the power supply unit that may cause overheating.
Product
AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: MD39543
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2186-2024·2024-07-03
Siemens Multix TOP X-ray Table Recalled Due to Fire Risk
Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2183-2024·2024-07-03
Siemens AXIOM MULTIX MP X-ray Tables Recalled for Power Supply Fire Risk
Siemens Medical Solutions is recalling AXIOM MULTIX MP radiographic X-ray tables due to a potential short circuit in the power supply that may cause overheating and fire. The recall includes 20 units with U.S. nationwide distribution.
Product
AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395431
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2185-2024·2024-07-03
AXIOM Vertix Solitaire Medical Imaging Device Recall: Fire Risk from Power Supply Defect
Siemens is recalling 4 AXIOM Vertix Solitaire medical imaging devices due to a short circuit in the touch display power supply that may cause overheating and fire. Units with serial numbers 1004, 1006, 1011, and 1014 are affected.
Product
AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24271·2024-06-20
myCharge POWER HUB Portable Chargers Recalled for Fire and Burn Hazards
myCharge is recalling about 567,000 POWER HUB All-In-One 10,000mAh portable chargers sold exclusively at Costco from January 2022 through November 2023 because they can overheat while charging, posing fire and burn hazards. Two residential fires and property damage totaling approximately $165,000 have been reported.
Product
myCharge POWER HUB All-In-One 10,000mAh portable chargers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1855-2024·2024-05-29
Philips Panorama HFO MR Systems Loose Terminal Connection May Create Fire Hazard
Philips Panorama HFO MR diagnostic imaging systems (Model 781350) contain a loose terminal connection in the mains distribution unit that may create a hotspot and cause smoke or fire. Approximately 118 units are affected worldwide.
Product
Panorama HFO- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781350
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1850-2024·2024-05-29
Philips Ingenia Ambition S MRI systems recalled for potential fire hazard
Philips is recalling Ingenia Ambition S MRI systems due to a potential fire hazard. A loose terminal connection in the electrical distribution unit may create a hotspot and smoke or fire in hospital technical rooms.
Product
Ingenia Ambition S Model Number (REF): (1) 782139; (2) 782133; (3) 782108; (4) 781359
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1884-2024·2024-05-29
Noblus AC Adapter for Ultrasound System Recalled for Smoke Hazard
FUJIFILM is recalling Noblus AC Adapters nationwide due to fire and smoke hazard. The adapters can overheat and generate smoke when the power cable is repeatedly inserted and removed.
Product
Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V301000·2024-04-29
Motorhome cooktop control boards can overheat and cause fire
Newmar is recalling certain 2022 Bay Star motorhomes because the LED backlight circuit board in the cooktop range may fail and overheat.
Product
NEWMAR — 2022 NEWMAR BAY STAR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V295000·2024-04-26
Winnebago motorhome cooktop circuit boards may fail and overheat
Winnebago Industries is recalling certain 2021-2025 motorhomes because the LED backlight circuit board in the cooktop range may fail and overheat. 1,166 units affected.
Product
WINNEBAGO — 2024 WINNEBAGO PORTO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1598-2024·2024-04-24
Siemens Artis X-ray systems cooling malfunction may halt procedures
Siemens Artis interventional X-ray systems may fail to cool the X-ray tube adequately, causing system shutdown and potentially requiring cancellation of clinical imaging procedures. The recall affects 583 units distributed nationwide.
Product
Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purpose- 10094139 Artis zee biplane- 10094141 Artis zeego- 10280959 Artis Q floor- 10848280 Artis Q ceiling- 10848281 Artis Q bipl
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V285000·2024-04-23
Winnebago towable cooktop circuit boards may fail and overheat
Winnebago Towable is recalling certain 2022-2024 travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat. 13,117 units affected.
Product
WINNEBAGO — 2024 WINNEBAGO HIKE200
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24159·2024-03-14
Insignia Air Fryers and Ovens Recalled for Fire and Burn Hazards
Best Buy is recalling about 187,400 Insignia brand air fryers and air fryer ovens sold from November 2021 through November 2023 because the units can overheat, causing handles to melt, glass doors to shatter, and fires.
Product
Air Fryers and Air Fryer Ovens
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24121·2024-02-15
Growing Table-Mini Greenhouse Recalled Due to Fire Hazard
Ocean State Job Lot is recalling approximately 12,800 Calipso "Combi" and Tiller & Rowe "Growing Table-Mini Greenhouse and Raised Garden Bed" products because they can overheat and pose a fire hazard that may result in property damage and injury. The firm received 10 reports of overheating, including one injury report.
Product
Calipso "Combi" and Tiller & Rowe "Growing Table-Mini Greenhouse and Raised Garden Bed"
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V054000·2024-01-30
Travel trailer cooktop control boards can overheat and cause fire
Winnebago is recalling certain 2022-2023 Micro Minnie, Micro Minnie FLX, Hike 200 and Minnie travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat.
Product
WINNEBAGO — 2022 WINNEBAGO MICRO MINNIE FLX
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24092·2024-01-25
Pacific Cycle Recalls Ascend Electric Bikes Due to Fire Hazard
Pacific Cycle is recalling about 1,700 Ascend Cabrillo and Minaret electric bikes because the battery charging wiring harness may overheat and catch fire while charging. The company has received three fire reports, including one causing second-degree burns.
Product
Ascend Cabrillo and Minaret Electric Bikes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0676-2024·2024-01-17
BD Recanalization System May Overheat or Break During Use
Bard Peripheral Vascular is recalling BD Recanalization Systems due to a manufacturing defect that may allow continuous operation without required safety warnings, increasing risk of device overheating or breaking during patient treatment.
Product
BD Recanalization System, REF: BDRECANSYSTEM
Category
Medical Device
Distribution
34 states