Hazard
809 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
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.
Viewrail recalls about 2,720 electronic LED modules used with floating stairs and rails due to a fire hazard. The modules can overheat and melt; 20 reports of overheating have been received, but no injuries have been reported.
Ford is recalling 2020-2024 Ford Escape and 2021-2024 Lincoln Corsair vehicles due to a high voltage battery manufacturing defect that may cause internal short circuits, loss of drive power, or fire risk.
Oliver Travel Trailers is recalling 2016-2024 Legacy Elite travel trailers with Truma Aqua Go water heaters. A loose burner bracket assembly may cause flame misdirection, increasing fire and burn injury risk.
BMW is recalling 2026 X4 and X6 vehicles with defective windshield seals that may allow water to enter electrical systems. This can cause loss of headlights and door functions, and may create fire hazards.
Deale International recalls about 2,900 Altafit af28 smartwatches sold by HSN due to fire and burn hazards from overheating wireless charging pads. The company received 39 reports of devices catching fire while charging, including six burn injuries and property damage.
LeymanKids children's pajama sets sold on AliExpress.com violate mandatory flammability standards for sleepwear, posing a burn injury risk. About 600 units were sold from March 2024 through May 2025.
Philips Ingenia Elition X MRI systems may have gradient coil component failures that could generate heat, smoke, and fire. Affected units were distributed worldwide including the United States.
Philips is recalling 1,467 Ingenia 3.0T MRI systems worldwide due to potential gradient coil component failures that could produce smoke or fire.
Philips is recalling 690 Ingenia Ambition X MR systems worldwide due to potential gradient coil component failures that could produce smoke or fire. Verify your device's model and serial number against the FDA recall list.
Philips Ingenia 1.5T MRI systems are recalled due to potential gradient coil component failures that may produce smoke or fire. The recall affects 2,279 units distributed worldwide.
Philips North America is recalling Ingenia 3.0T CX MRI systems worldwide due to potential gradient coil failures that may produce smoke and fire. About 350 units are affected.
Philips is recalling MR 7700 imaging systems due to potential component failures in the gradient coil that may produce smoke and fire. The recall affects 82 units distributed worldwide.
Philips is recalling 93 MRI systems with defective gradient coil components that may produce smoke or fire due to component failure.
Philips is recalling 50 Evolution Upgrade 3.0T MRI systems worldwide due to potential fire and smoke from gradient coil component failures.
Philips is recalling 294 SmartPath to dStream MRI systems due to potential component failures in the gradient coil that could produce smoke and fire. No injuries have been reported.
Philips is recalling 611 Ingenia Ambition S MRI systems due to potential gradient coil component failures that could generate heat, smoke, or fire. The affected units were distributed worldwide.
Philips North America is recalling 136 Ingenia MRI systems due to potential gradient coil failures that could generate heat and produce smoke or fire. The affected units have been distributed worldwide.
Philips is recalling the MR 7700 imaging system upgrade due to potential Gradient Coil component failures that could generate heat, smoke, and fire. The recall affects 26 units with worldwide distribution.
Philips is recalling certain SmartPath to Ingenia Elition X magnetic resonance imaging systems due to potential gradient coil component failures that could generate heat and produce smoke or fire. Approximately 33 units are affected worldwide.
Philips North America is recalling Achieva 3.0T MRI systems due to potential gradient coil component failures that could produce smoke or fire. The recall affects 460 units distributed worldwide.
Philips is recalling Intera 3.0T Quasar Dual MRI systems worldwide due to potential gradient coil failures that could generate smoke or fire.
Philips is recalling 242 Ingenia Elition S MRI systems worldwide due to potential gradient coil component failures that could produce smoke and fire. Affected facilities should immediately stop using the systems.
Philips is recalling Achieva XR MRI systems (Models 781153, 781253) due to potential fire and smoke hazard from gradient coil component failures. Approximately 40 units distributed worldwide.
Philips MRI systems with affected gradient coils may experience component failures that could produce smoke or fire. Fifteen units worldwide are affected.
Philips is recalling certain MR 5300 magnetic resonance imaging systems due to potential gradient coil component failures that could generate heat, smoke, or fire. The recall affects 551 units distributed worldwide, including the United States.