The Recall Desk

Hazard

Fire Risk recalls

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

What the numbers show

Total
94
Critical
6
Severe
17
Most recent
2026-08-12

Of the 94 fire risk recalls we have scored against our rubric, 6 (6%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 17 (18%) 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 fire risk 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.

1–25 of 94

  • SevereFDA (Devices)·Z-2857-2026·2026-08-12

    OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating

    OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.

    Product
    Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V380000·2026-06-09

    Midwest Automotive Design motorhome ground cables may be undersized

    Alliance RV is recalling certain Midwest Automotive Design recreational vehicles because the ground wire may be undersized for the electrical system, risking overheating and fire.

    Product
    MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN ULTIMATE TRAVELER, PROFESSIONAL SERIES, ATHLETIC SERIES, BUSINESS CLASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V352000·2026-05-29

    Forest River travel trailer fireplace outlets may have incorrect wiring

    Forest River is recalling certain 2024-2026 Wildwood and Salem travel trailers because the fireplace outlet may have incorrect wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO, SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V324000·2026-05-20

    Alliance RV trailer battery heating pads may not suit lithium batteries

    Alliance RV is recalling certain 2022-2025 Valor and Paradigm recreational trailers because the heating pad may not be appropriate for lithium battery applications.

    Product
    ALLIANCE RV — ALLIANCE RV VALOR, PARADIGM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V308000·2026-05-14

    Hyundai Elantra Hybrid power control units may overheat

    Hyundai is recalling certain 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit assembly may overheat, increasing the risk of a fire. 54,337 vehicles are affected.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1942-2026·2026-05-13

    VOCSN V+Pro Ventilator System Respiratory Device Safety Recall

    Ventec Life Systems is recalling VOCSN V+Pro ventilator units because they may not have been fully tested for high-pressure conditions, which could cause oxygen leaks and increase fire risk during use.

    Product
    VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
    Category
    Medical Device
    Distribution
    4 states
  • SevereNHTSA·26V258000·2026-04-22

    Volkswagen Taos fuel pressure sensor may separate in a rear-end crash

    Volkswagen is recalling certain 2025-2026 Taos vehicles because the fuel pressure sensor may dislodge from the fuel tank in a rear-end crash, failing FMVSS 301 fuel system integrity.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V214000·2026-04-02

    BMW motorcycles recalled over a reverse gear unit that may overheat

    BMW of North America is recalling 9,160 K 1600 motorcycles because a deteriorating seal can let moisture into the reverse gear control unit, causing it to overheat.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 GRAND AMERICA, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1436-2026·2026-03-04

    MRI LED Mobile Exam Light Battery REF SL-111 Recalled Due to Overheating

    MRIMed Inc. is recalling 314 MRI LED Mobile Exam Light Batteries due to battery component overheating while charging, which can cause internal component melting and smoke.

    Product
    MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1147-2026·2026-01-28

    Full electric lightweight homecare beds recalled over pendants that may overheat

    Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-inv
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1014-2026·2026-01-28

    Full electric low homecare beds recalled over hand pendants that overheat

    Medline is recalling 22,565 units of the Full Electric Low Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1016-2026·2026-01-28

    Full electric low lightweight homecare beds recalled over overheating pendants

    Medline is recalling 15,581 units of the Full Electric Low Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1013-2026·2026-01-28

    Full electric basic homecare beds recalled over pendants that may overheat

    Medline is recalling 138,412 units of the Full Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1012-2026·2026-01-28

    Semi electric lightweight homecare beds recalled over pendants that may overheat

    Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
    Category
    Medical Device
    Distribution
    4 states
  • CriticalCPSC·26215·2026-01-22

    Semi electric homecare beds recalled over hand pendants that may overheat

    Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Mikario Trading 5-in-1 Convertible Baby Gyms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V610000·2025-09-12

    Travel trailers recalled because inlet wiring may arc and cause fire

    Forest River is recalling certain 2025-2026 Spirit and Shasta Oasis recreational trailers because the 30 or 50 amp inlet wire sheathing may be inconsistently stripped, causing electrical arcing. 502 units are affected.

    Product
    FOREST RIVER — FOREST RIVER SHASTA OASIS, SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V597000·2025-09-11

    Ford Bronco and Ranger recalled over fuel pump bolts that may leak

    Ford is recalling certain 2024 Bronco and Ranger vehicles because the bolts securing the high pressure fuel pump may not be tightened properly, which can result in a fuel leak. 9 units are affected.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V467000·2025-07-11

    Ford Bronco Sport and Escape fuel injectors may crack and leak

    Ford is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles with 1.5L engines because a fuel injector may crack and leak fuel inside the engine compartment. 694,271 vehicles affected.

    Product
    FORD — FORD BRONCO SPORT, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25322·2025-06-05

    Apollo America Combination Smoke and Carbon Monoxide Detectors Recalled

    Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.

    Product
    Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V202000·2025-04-01

    2025 BMW vehicles recalled for loose starter-generator connection defect

    BMW is recalling certain 2025 BMW vehicles because the electrical connection between the starter-generator and battery may come loose, potentially causing engine stall or fire.

    Product
    BMW — BMW 430I, 330I, X3, 430I XDRIVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V860000·2024-11-14

    2022 Indian FTR1200 Motorcycles Recalled for Fuel Tank Leak Risk

    Indian Motorcycle Company is recalling certain 2022 FTR1200 motorcycles due to fuel tanks with holes that may leak fuel, increasing the risk of fire or injury. Dealers will replace the fuel tank free of charge.

    Product
    INDIAN — INDIAN FTR1200, FTR 1200 R CARBON, FTR 1200 S, FTR 1200 RALLY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0222-2025·2024-11-06

    Ambulatory Infusion System Batteries May Short Circuit and Overheat

    CADD-Solis battery packs used in ambulatory infusion systems may develop internal short circuits causing battery case melting and charging circuit failure. The FDA Class I recall affects 138,039 units worldwide.

    Product
    CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD Solis Ambulatory Infusion Systems: 21-2101-0100-50, 21-2101-0200-02, 21-2101-0200-03, 21-2101-0200-06, 21-2101-0200-07, 21-2101-0200-12, 21-2101-0200-14, 21-210
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0216-2025·2024-10-30

    Baxter Operating Table TruSystem 7000 recalled for battery electrical hazards

    Baxter Healthcare is recalling the TruSystem 7000 (dV) V operating table worldwide due to batteries and connectors that may experience electrical short-circuits and emit smoke.

    Product
    Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
    Category
    Medical Device
    Distribution
    0 states