The Recall Desk

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.

1076–1100 of 2084

  • SevereFDA (Devices)·Z-1150-2013·2013-04-24

    Advanced Sterilization Products Recalls EVOTECH Endoscope Cleaner Due to Smoke Risk

    Advanced Sterilization Products is recalling 761 EVOTECH Endoscope Cleaner and Reprocessor systems because a circuit board malfunction can cause smoke to emanate from the device.

    Product
    EVOTECH Endoscope Cleaner and Reprocessor System, P/N 50004. Designed to automatically clean and high-level disinfect flexible, submersible video or fiber-optic endoscopes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V161000·2013-04-24

    Winnebago and Itasca Motorhomes Recalled for Missing Range Enclosure

    Winnebago is recalling 2012-2014 motorhomes because a missing range enclosure may allow propane gas to flow without a flame, creating a fire hazard.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA MINNIE WINNIE, CAMBRIA, MERIDIAN, SUNCRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1081-2013·2013-04-17

    Siemens ACUSON SC2000 Ultrasound System Recalled for Temperature Display Error

    Siemens is recalling ACUSON SC2000 ultrasound systems with specific hardware due to a temperature display error that may underestimate transducer heat, posing a burn risk.

    Product
    Siemens brand ACUSON SC2000 Ultrasound System, Model 10433816, hardware that contains version 4 of the MPI board 10434200; The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult C
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·13171·2013-04-17

    Gerbings Recalls 12-Volt Heated Jacket Liners Due to Burn Hazard

    Gerbings is recalling about 9,900 12-volt heated jacket liners sold at Harley-Davidson dealerships and other stores because a defective wire connector can cause overheating and minor burns.

    Product
    12-volt heated jacket liners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1096-2013·2013-04-17

    GE Healthcare Recalls LOGIQ Ultrasound Systems Due to Potential Skin Burn Risk

    GE Healthcare is recalling LOGIQ S8 and S7 ultrasound systems equipped with the S4-10-D probe due to a potential safety issue that may cause skin burns.

    Product
    GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) and LOGIQ S7 (with software revisions R1.0.1, R1.0.2 and R1.0.3) diagnostic ultrasound system with the S4-10-D Ultrasound Probe. The device is intended for use in ultrasound evaluation.
    Category
    Medical Device
    Distribution
    40 states
  • HighNHTSA·13E018000·2013-04-15

    Schneider Electric Recalls EVlink Charging Stations for Overheating Risk

    Schneider Electric is recalling specific EVlink charging stations because the charger plug pin connectors may overheat, potentially melting the casing and causing burns or damage.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0946-2013·2013-03-20

    Natus Neurology Recalls Nicolet EEG Wireless Amplifiers Due to Overheating Risk

    Natus Neurology is recalling 114 Nicolet EEG Wireless Amplifiers because they may overheat near the on/off button, posing a risk of discomfort or burns.

    Product
    Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers : 515-015400 for the 32 channel amplifier and 515-015500 for the 64 channel amplifier. Product Usage: The Nicolet Wireless EEG Amplifier is intended to be used as a front end amplifier to acquire, store, and t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13124·2013-02-26

    Ryobi Lithium 18 V 4Ah Battery Pack Recalled for Fire and Burn Hazards

    One World Technologies is recalling Ryobi Lithium 18 V 4Ah battery packs because they can overheat and burst while charging, posing fire and burn risks.

    Product
    Ryobi Lithium 18 V 4Ah Battery Pack
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0784-2013·2013-02-13

    Lansinoh Thera Pearl Breast Therapy Hot and Cold Packs Recalled for Overheating Risk

    Lansinoh is recalling Thera Pearl 3-in-1 Breast Therapy packs because incorrect Spanish heating instructions may cause the product to overheat.

    Product
    THERA PEARL 3-in-1 BREAST THERAPY, 2 hot and cold packs in plastic box. The Thera Pearl 3-in-1 Breast Therapy is a reusable therapeutic hot and cold pack for use with pain, swelling, engorgement, plugged ducts or mastitis associated with breast feeding or to help encourage l
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13104·2013-01-29

    Columbia Recalls Seven Heated Jacket Models Due to Burn Hazard

    Columbia Sportswear is recalling seven models of heated jackets because the inner wrist cuffs can overheat, posing a burn risk.

    Product
    Men's and Women's Heated Jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13095·2013-01-15

    Target Recalls Circo Girls' Fleece Pajamas for Flammability Violation

    Target is recalling Circo girls' fleece pajamas because they fail to meet federal flammability standards, posing a risk of burn injuries to children.

    Product
    Girls' Circo Fleece Blanket Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0620-2013·2013-01-09

    SynCardia Recalls Companion External Batteries Due to Thermal Event Risk

    SynCardia Systems is recalling Companion External Batteries used with the Companion 2 Driver System because they may be at risk of thermal events or physical damage.

    Product
    Companion External Battery, Part Number: 293001-001 The Companion External Battery is a component of the Companion 2 Driver System and the Companion Driver System. Both Driver Systems, with the temporary Total Artificial Heart (TAH-t) are indicated for use as a bridge to trans
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0525-2013·2013-01-02

    Praxair Vantage Grab n Go Gas Cylinder Pressure Regulator Recall

    Praxair Inc. is recalling Vantage Grab n Go gas cylinder pressure regulators due to isolated incidents of ignition inside cylinders subjected to significant physical impact.

    Product
    Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Catalog Number: OX-M-AEGNGVNTG Usage: Regulator reduces pressure in oxygen-containing cylinder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0616-2013·2013-01-02

    Brookstone Recalls Heated Body Beans Due to Burn Risk

    Brookstone is recalling 109,956 electrically heated body bean products nationwide due to a risk of skin burns.

    Product
    Brookstone Heated Body Bean, electrically heated SKU numbers: 734863 (Blue), 734864 (Plum), 734865 (Red). Brookstone 3 in 1 wrap ,SKU734397 (Brown). The Products are liquid filled bean shaped pouches that are electrically heated and then detached from the charger prior to u
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2013·2012-12-26

    Bunnell Patient Circuits Recalled Due to Heater Wire Insulation Melting

    Bunnell, Inc. is recalling Patient Circuits used with the Life Pulse High Frequency Ventilator because heater wire insulation can melt, causing sparking and smoke.

    Product
    Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a required disposable component of the Life Pulse High Frequency Ventilator. Model #(s): Individual Patient Circuit - catalog # 902 Patient Circuit Kit - catalog # 937: contains 2 circu
    Category
    Medical Device
    Distribution
    Distributed nationwide