Hazard

Burn Injury recalls

2,084 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 2,084
Critical: 32
Severe: 734
Most recent: 2026-09-10

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

About this hazard tag

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.

251–275 of 2084

HighFDA (Devices)·Z-2231-2023·2023-08-02
Flexiva Pulse ID Laser Fiber Recalled for Incorrect Component
Boston Scientific is recalling Flexiva Pulse ID laser fibers due to an incorrect component that reduces power output and aiming beam brightness. The component can overheat, risking burns to users who touch the fiber connector.
Product
Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy Single-pack UPN: M006L8406910
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2016-2023·2023-07-26
Olympus Bronchovideoscope Recalled for Endobronchial Combustion Risk
Olympus is recalling 17,609 bronchovideoscope units nationwide due to complaints of endobronchial combustion during therapeutic laser procedures, which poses a fire and burn risk to patients.
Product
Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-P180, BF-Q180, BF-Q180-AC, BF-1T180, BF-1TQ180
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2017-2023·2023-07-26
Olympus EVIS EXERA III Bronchovideoscope Combustion Hazard Recall
Olympus is recalling EVIS EXERA III Bronchovideoscopes nationwide due to complaints of endobronchial combustion during therapeutic laser procedures. This FDA Class I recall affects approximately 9,684 units.
Product
Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2011-2023·2023-07-26
Olympus OES Bronchofiberscope Models Recalled for Combustion Risk During Laser Procedures
Olympus is recalling OES Bronchofiberscope models due to reports of combustion during laser procedures. This poses a serious burn injury risk to patients.
Product
Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2014-2023·2023-07-26
Olympus EVIS EXERA Bronchoscope Recalled for Combustion Risk During Laser Procedures
The FDA recalls 284 Olympus EVIS EXERA bronchoscopes due to complaints of combustion during therapeutic laser procedures. Users should stop using affected models immediately.
Product
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2013-2023·2023-07-26
Olympus Bronchoscope Recall: Risk of Combustion During Laser Procedures
Olympus is recalling 9 bronchoscopes (Models BF-P150 and BF-1T150) due to complaints of endobronchial combustion during therapeutic laser procedures. The defect could cause fire and serious burn injuries.
Product
Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2012-2023·2023-07-26
Olympus Bronchofiberscope BF Type recalled for combustion risk during laser procedures
Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.
Product
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1994-2023·2023-07-05
MEGADYNE MEGA 2000 Patient Return Electrode Recalled Due to Patient Burns
The FDA is recalling 21,100 units of the MEGADYNE MEGA 2000 Patient Return Electrode due to reports of patient burns during electrosurgical procedures. All units distributed nationwide are affected.
Product
MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2000-2023·2023-07-05
MEGADYNE MEGA SOFT Return Electrode Recalled for Burns During Surgical Procedures
Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode due to reported patient burns that occurred during electrosurgical procedures.
Product
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1999-2023·2023-07-05
MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode Recalled for Patient Burns
Megadyne Medical Products is recalling 21,100 units of MEGA SOFT Universal Plus Patient Return Electrodes used in electrosurgery. The FDA Class I recall follows reports of patient burns during surgical procedures.
Product
MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1995-2023·2023-07-05
MEGADYNE MEGA SOFT Reusable Patient Return Electrode Recalled for Patient Burn Hazard
Megadyne Medical Products is recalling 21,100 MEGADYNE MEGA SOFT Reusable Patient Return Electrodes nationwide due to reports of patient burns during electrosurgical procedures.
Product
MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2001-2023·2023-07-05
Megadyne Mega Soft Universal Patient Return Electrode Recalled for Burn Risk
Megadyne Medical Products is recalling 21,100 MEGA SOFT electrosurgery patient return electrodes distributed nationwide due to reports of patient burns during surgical procedures.
Product
MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1997-2023·2023-07-05
Pediatric Patient Return Electrode Recalled for Reported Burns in Surgery
Megadyne Medical Products recalls approximately 21,100 MEGADYNE MEGA SOFT Pediatric Patient Return Electrodes (Model 0840) due to reports of patient burns during electrosurgical procedures.
Product
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1998-2023·2023-07-05
Patient Return Electrode Recalled Due to Burn Reports During Surgery
Megadyne Medical Products is recalling MEGA SOFT Universal Patient Return Electrodes after reports of patient burns during electrosurgery procedures. The FDA classified this as a Class I recall.
Product
MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1996-2023·2023-07-05
MEGADYNE MEGA SOFT Patient Return Electrode Recalled for Reported Patient Burns
Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode used in electrosurgery due to reports of patient burns during surgical procedures.
Product
MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1633-2023·2023-06-14
FDA Recalls Walnut Wearable Smart Thermometer Due to Reported Skin Burns
BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.
Product
Walnut Wearable Smart Thermometer, intended for continuous chest temperature monitoring of children ages 0-6 years in non-emergency medical situations, Model Number WT20
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·23767·2023-06-08
Children's Pajamas and Nightdresses Recalled for Flammability Hazard
Little Cotton Clothes children's pajamas and nightdresses fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 550 units were sold online and in children's clothing stores from September 2022 through January 2023.
Product
Little Cotton Clothes Pajamas and Nightdresses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23766·2023-06-08
Deux Par Deux Children's Pajamas Recalled for Flammability Standards Violation
Deux Par Deux children's one-piece and two-piece pajama sets fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. About 90 units sold online from January to February 2023 are affected.
Product
Deux Par Deux Children's One-Piece and Two-Piece Pajama Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2023·2023-05-31
Olympus Single Use Distal Cover for Endoscope Recalled Due to Detachment Risk
Olympus is recalling about 309,278 single-use endoscope covers that may detach during use, risking aspiration, inhalation, obstruction, or burns.
Product
Olympus Single Use Distal Cover Model Number MAJ-2315 used with EVIS EXERA III Duodenovideoscope TJF-Q190V; Item code: Catalogue #N5786100
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V378000·2023-05-26
Ford Recalls 2015-2019 Lincoln MKC for Engine Compartment Fire Risk
Ford is recalling 2015-2019 Lincoln MKC vehicles because a battery monitor sensor may short-circuit and overheat, causing a fire in the engine compartment.
Product
LINCOLN — LINCOLN MKC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1600-2023·2023-05-24
Fisher Wallace Stimulator Models Recalled for Battery Overheat and Burn Risk
Fisher Wallace Stimulator Models FW-100 and FW-200 are being recalled because incorrectly installed batteries may cause the device to overheat, potentially resulting in burns. The recall affects 43,489 devices distributed nationwide and globally.
Product
Fisher Wallace Stimulator Models FW-100 and FW-200
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·23204·2023-05-18
Target Recalls 4.9 Million Threshold Glass Jar Candles for Laceration and Burn Risk
Target is recalling approximately 4.9 million Threshold Glass Jar Candles because the glass jar can crack or break during use, posing laceration and burn hazards. Six injuries, including lacerations and severe burns, have been reported.
Product
Threshold Glass Jar Candles
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23205·2023-05-18
PowerXL Stuffed Wafflizer Waffle Makers Recalled for Burn Hazard
About 456,000 PowerXL Stuffed Wafflizer waffle makers are being recalled because hot pieces of waffle or stuffing can be expelled during use or when opening the product, creating a burn risk. The firm has received 44 incident reports, including 34 burn injuries with three requiring medical attention.
Product
PowerXL Stuffed Wafflizer waffle makers
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23206·2023-05-18
Kell Electronic Personal Chiller Mini Refrigerators Recalled for Burn Hazard
Kell Electronic is recalling about 25,000 Personal Chiller Mini Fridge Gamer Beverage Refrigerators with LED Lights because the power cord can overheat and cause burns. No injuries have been reported.
Product
Personal Chiller Mini Fridge Gamer Beverage Refrigerators with LED Lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23751·2023-05-04
Polaris Model Year 2022-2023 Snowmobiles Recalled for Fire Hazard
Polaris is recalling about 14,885 Model Year 2022-2023 MATRYX RMK KHAOS and PRO snowmobiles. When the rider engages the throttle and brake simultaneously, the brake system can overheat, posing a fire hazard and risk of burn injuries.
Product
Model Year 2022-2023 MATRYX RMK KHAOS and PRO Snowmobiles
Category
Vehicle
Distribution
Distributed nationwide