Hazard

Fire recalls

809 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 fire 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.

376–400 of 809

HighFDA (Devices)·Z-2041-2024·2024-06-19
MRI Systems Power Cable Terminal Block Fire Hazard Recall
Canon Medical MRI systems are being recalled because the terminal block securing the power cable may disconnect, potentially causing electrical arcing and fire. 153 units are affected across the United States and Puerto Rico.
Product
MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504), Vantage Titan 3T MRT-3010 (MEXL-3010), Vantage Galan 3T MRT-3020 (MEXL-3020)
Category
Medical Device
Distribution
38 states
SevereCPSC·24262·2024-06-13
Southern Telecom Recalls Lomi Roll-On Waxing Kits for Fire and Shock Hazards
Southern Telecom is recalling about 19,500 Lomi Roll-On Waxing Kits because the power cord can overheat and short circuit, creating fire, burn, and electrical shock hazards. Two consumers suffered burns and one incident of property damage has been reported.
Product
Lomi Roll-On Waxing Kits
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24260·2024-06-13
Daikin Air Conditioning and Heat Pump Units Recalled for Fire Hazard
Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.
Product
Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V655000·2024-06-09
Phoenix Motorcars Transit Buses Recalled for Electrical System Fire Risk
Phoenix Motorcars is recalling certain 2019-2021 800V Catalyst and 2020-2022 ZX5 transit buses. The vehicle software may cause the radiator fan electrical circuit to overheat, increasing fire risk.
Product
PROTERRA — 2020 PROTERRA ZX5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V655000·2024-06-08
Motorhomes with improperly routed hydraulic lines pose fire risk
REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.
Product
FLEETWOOD — 2020 FLEETWOOD BOUNDER
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24254·2024-06-06
Good Earth Rechargeable Integrated Lights Recalled for Fire and Burn Hazards
Good Earth Lighting is recalling more than 1.2 million rechargeable integrated lights whose lithium-ion batteries can overheat and ignite the plastic housing, posing fire and burn hazards. One death has been reported.
Product
Good Earth Rechargeable Integrated Lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24256·2024-06-06
Kawasaki Engines in Multiple Lawn Equipment Brands Recalled for Fire and Burn Hazard
Kawasaki is recalling approximately 68,500 engines used in lawn and garden equipment from multiple brands due to overheating that can cause fire and burn hazards. Consumers should stop using affected equipment and contact the manufacturer or an authorized dealer for free repair.
Product
Kawasaki Engines used in Bad Boy Mowers, BigDog, Bobcat, Cub Cadet, Hustler, John Deere, and Kubota brand lawn and garden equipment
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V357000·2024-06-05
Altec Aerial Devices Recalled for Water Intrusion Fire Risk
Altec is recalling 2021-2023 aerial devices, digger derricks, and related equipment because water can leak into strobe lights, causing electrical short-circuits that increase fire risk. No injuries have been reported.
Product
ALTEC — 2021 ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1931-2024·2024-06-05
BD Pyxis Anesthesia Station ES units recalled for potential fire and smoke risk
CareFusion 303, Inc. is recalling approximately 71,569 BD Pyxis Anesthesia Station ES units worldwide due to potential fluid ingress that could cause smoke, system downtime, or fire.
Product
BD Pyxis" Anesthesia Station ES, REF: 327
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1930-2024·2024-06-05
BD Pyxis MedStation 4000 Auxiliary Tower: Potential Fluid Ingress Fire Risk
The BD Pyxis MedStation 4000 Auxiliary Tower may allow fluid to enter the system, potentially causing smoke, system downtime, and fire. The FDA Class II recall affects 35,029 units distributed worldwide.
Product
BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1928-2024·2024-06-05
BD Pyxis MedStation 4000 Medication Cabinet Fire Risk Recall
CareFusion 303, Inc. is recalling approximately 91,933 units of the BD Pyxis MedStation 4000 System medication cabinet worldwide due to potential fluid ingress that may cause smoke, fire, or system downtime.
Product
BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1927-2024·2024-06-05
BD Pyxis MedStation ES Medication Cabinet Fluid Ingress Fire Hazard
BD Pyxis MedStation ES medication cabinets may experience fluid ingress, potentially causing smoke, fire, or system downtime. CareFusion is recalling 212,367 units globally.
Product
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V387000·2024-06-05
2021-2022 Escape Travel Trailers Recalled for Cracked LP Gas Fittings
Escape Trailer is recalling 2021-2022 Escape travel trailers (models 17, 19, 21, and 5.0TA) due to cracked quick disconnect fittings in the LP gas system that may cause a gas leak and fire hazard.
Product
ESCAPE — 2021 ESCAPE ESCAPE 21
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1932-2024·2024-06-05
BD Pyxis Anesthesia Station 4000 Recalled for Fluid Ingress Fire Risk
CareFusion's BD Pyxis Anesthesia Station 4000 is recalled due to potential fluid ingress that may cause smoke, fire, or system downtime. The recall involves 11,875 units distributed worldwide.
Product
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2024·2024-05-29
Medical Device Mains Distribution Unit Recall Due to Fire Risk
The Evolution upgrade 3.0T mains distribution unit is being recalled because its L3 terminal connection may become loose, creating a hotspot that could cause fire or smoke in hospital technical rooms.
Product
Evolution upgrade 3.0T Model Number (REF): (1)782117; (2) 782143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1865-2024·2024-05-29
Philips dStream MR System Terminal Connection May Become Loose and Cause Fire
Philips is recalling its Upgrade dStream MR system due to a potential fire hazard. A loose terminal connection in the g-MDU may create a hotspot causing smoke or fire.
Product
Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 782127
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2024·2024-05-29
Philips MR 5300 magnetic resonance systems' mains distribution unit may ignite
Philips has recalled 81 MR 5300 MRI systems worldwide due to a loose electrical connection that may overheat and cause fire or smoke in hospital technical rooms.
Product
MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): (1) 782152 (2) 782110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1841-2024·2024-05-29
Philips Achieva 3.0T PET imaging device poses potential fire hazard
A loose terminal connection in the power distribution unit of Philips Achieva 3.0T TX PET imaging systems may create an electrical hotspot, potentially causing smoke or fire. The device is distributed worldwide.
Product
Achieva 3.0T TX for PET Model Number (REF): 781479
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1840-2024·2024-05-29
Medical MR System Electrical Terminal Connection May Create Fire Hazard
A Philips Achieva 3.0T for PET MR diagnostic system (Serial 43006) may have a loose mains distribution unit terminal that could overheat and cause smoke or fire.
Product
Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 781477
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1846-2024·2024-05-29
Philips Ingenia MR Systems Recalled for Fire Risk From Loose Connector
Philips is recalling Ingenia 1.5T CX Magnetic Resonance systems due to a loose power distribution connection that may create a fire hazard in hospital technical rooms.
Product
Ingenia 1.5T CX - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): (1) 781262 (2) 781261
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1842-2024·2024-05-29
MR Imaging System Recall for Loose Electrical Terminal Connection Fire Risk
Philips AchievaXR MR systems may have loose terminal connections in the power distribution unit that could create hotspots and cause smoke or fire. The FDA has recalled 35 affected units worldwide.
Product
AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 781253
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1847-2024·2024-05-29
Philips Ingenia MRI Scanner Mains Distribution Unit Fire Risk Recall
Philips is recalling 139 Ingenia 1.5T S MRI scanners due to a loose terminal connection in the power distribution unit that could create an electrical hotspot and cause smoke or fire. No injuries have been reported.
Product
Ingenia 1.5T S Model Number (REF): 781347
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1856-2024·2024-05-29
Medical Imaging System Recalled Due to Fire Risk from Loose Connection
Philips has recalled 81 Marlin 1.5T MR diagnostic systems due to a loose g-MDU terminal connection that may create a fire hazard in hospital technical rooms.
Product
Marlin 1.5T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781474
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1862-2024·2024-05-29
Philips MR Systems Recalled for Loose Electrical Connection Fire Hazard
Philips has recalled 200 SmartPath to dStream MR imaging systems worldwide due to a loose electrical connection in the g-MDU unit that may create a fire hazard in hospital technical rooms.
Product
SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): (1) 782129; (2) 782113; (3) 781270
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1863-2024·2024-05-29
Philips MRI System Recall: Loose Electrical Terminal May Cause Fire
Philips MRI diagnostic systems are recalled because a loose electrical connection in the g-MDU unit may create a hotspot, potentially causing fire and smoke in hospital technical areas.
Product
SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 782118
Category
Medical Device
Distribution
Distributed nationwide