Hazard
2,084 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,084 burn injury recalls we have scored against our rubric, 32 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 734 (35%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all burn injury 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.
Fully Popped is recalling Poppin' Cobs 10 Pack Microwave Popcorn because the paper bags can catch fire in the microwave, posing fire and burn hazards.
Noah Clothing is recalling men's reverse fleece hoodies because they fail federal flammability standards, posing a burn risk. No injuries have been reported.
Epson is recalling power adapters sold with V-series scanners because they can overheat, melt, and catch fire. Consumers should stop using them and contact Epson for a free replacement.
Modular Robotics is recalling about 2,400 rechargeable battery packs because they can short circuit and overheat, posing a burn hazard.
Gillig is recalling 2018-2020 Low Floor CNG buses because the pressure relief device may fail to vent heat, risking system rupture and injury.
KT Health, LLC is recalling 94,554 KT RECOVERY+ Ice/Heat Massage Balls because overheating may cause leaks, potentially exposing users to hot fluid.
Solta Medical is recalling Thermage Face Tip 3.0 units because sparking during use could cause skin burns.
Pass & Seymour is recalling about 685,000 commercial-grade electrical receptacles because a manufacturing error could cause plug blades to overheat, posing a burn risk.
Continuum is recalling Lenox 2.5 Quart Tea Kettles because they can expel hot water, posing a burn hazard. Consumers should stop using the kettles and contact the company for a refund.
Agility Fuel Solutions is recalling certain CNG pressure relief devices that may fail to vent when exposed to heat, potentially causing the fuel system to rupture.
Ra Medical Systems is recalling 10 Pharos EX-308 Excimer Laser units because a software error may prevent the device from stopping, potentially causing skin burns.
Hawthorne Hydroponics is recalling approximately 60,000 Grower's Edge Vaporizers because they can overheat, causing burns, fires, or electrical shocks.
Kawasaki is recalling about 72,000 MULE PRO off-highway utility vehicles because debris can ignite on the exhaust manifold and oil leaks can cause fires.
American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.
Yamaha is recalling Line 6 Relay G10 wireless guitar systems because the lithium-ion battery can overheat and the cover can separate, posing fire and injury risks.
Joules USA is recalling specific children's pajamas and robes because they violate federal flammability standards, posing a burn hazard to children.
Ishtex Textile Products is recalling Just Blanks children's nightgowns because they fail to meet federal flammability standards, posing a burn hazard.
Pacific Medical Group is recalling 6,481 Button-Style Ultrasound Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal and maternal monitoring or patient burns.
Pacific Medical Group is recalling Loop-Style Tocotransducers serviced with unverified non-OEM components, which may cause inaccurate fetal monitoring or patient burns.
Pacific Medical Group is recalling 1,994 ultrasound transducers serviced with unverified non-OEM components, which may cause inaccurate fetal and maternal monitoring.
Pacific Medical Group Inc. is recalling Toco MP Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal monitoring and patient burns.
Pacific Medical Group is recalling 1,603 External Toco Transducers serviced with non-OEM parts that were not appropriately verified or validated.
Pacific Medical Group is recalling 9,679 Button-Style Tocotransducers serviced with non-OEM components that were not appropriately verified, posing risks of inaccurate monitoring and burns.
Pacific Medical Group is recalling 2,170 Toco+ transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal/maternal monitoring and patient burns.
Pacific Medical Group is recalling 466 Toco M2734A fetal monitors serviced with unverified non-OEM components that may fail to detect fetal distress or cause burns.