The Recall Desk

Hazard

Electrical Failure recalls

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

What the numbers show

Total
146
Critical
1
Severe
49
Most recent
2026-08-14

Of the 146 electrical failure recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 49 (34%) 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 electrical failure 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.

26–50 of 146

  • HighNHTSA·23V312000·2023-05-03

    Volkswagen ID.4 Door Handles May Open Unexpectedly Due to Water Intrusion

    Certain 2021-2022 Volkswagen ID.4 vehicles have door handles that may allow water to enter the circuit board assembly, potentially causing doors to open unexpectedly while driving. Volkswagen will update vehicle software and inspect door handles at no cost to owners.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1313-2023·2023-04-19

    Ivenix Large Volume Infusion Pump Recalled Due to Fluid Ingress Risk

    Fresenius Kabi is recalling the Ivenix Infusion System Large Volume Pump (Model LVP-0004) because fluid ingress can damage the device, causing loss of electrical function and preventing or halting infusion.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump, Model No. LVP-0004
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·23V080000·2023-02-14

    2019-2022 Subaru Crosstrek Hybrid battery charging system recall

    Subaru is recalling 2019-2022 Crosstrek Hybrid vehicles because the harness terminal supplying power to the 12-Volt battery may corrode and break, preventing charging. A non-functioning battery can cause loss of drive power and increase crash risk.

    Product
    SUBARU — SUBARU CROSSTREK HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V861000·2022-11-21

    Audi vehicles recalled for gateway control module failure causing engine power loss

    Volkswagen Group is recalling 2019-2022 Audi sedans, wagons, and allroad models. Liquid in the rear seat may penetrate and shut down the gateway control module, suddenly reducing engine power and increasing crash risk.

    Product
    AUDI — AUDI A6 ALLROAD, S6, A7, S7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V733000·2022-09-30

    2020 Mercedes-Benz CLS450 improperly secured battery defect recall

    Mercedes-Benz is recalling 2019-2022 CLS450 and related models. The 12V battery in the trunk may not be properly secured, which could cause electrical failure and disable safety features like the emergency call system, hazard lights, and automatic door locks in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, AMG E53, AMG CLS53, CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V635000·2022-08-19

    Indian Motorcycle Recalls 28,689 Models for Electrical Connection Failure

    Indian Motorcycle is recalling 28,689 motorcycles from 2014-2020 because a failing electrical connection may cause loss of front lights, increasing crash risk.

    Product
    INDIAN — INDIAN CHIEFTAIN DARK HORSE, CHIEFTAIN, CHIEF VINTAGE, SPRINGFIELD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1467-2022·2022-08-03

    TruClear Hysteroscopic Tissue Removal Control Unit Electrical Failure

    Covidien is recalling 33 TruClear Hysteroscopic Tissue Removal System Control Units due to electrical component failure causing loss of device function during surgery. The affected units were distributed to multiple U.S. states and foreign countries.

    Product
    TruClear Hysteroscopic Tissue Removal System Control Unit- designed to meet the requirements of intrauterine tissue removal. Model Number: 7209808
    Category
    Medical Device
    Distribution
    15 states
  • HighCPSC·22763·2022-07-28

    Arctic Cat Alterra 600 and Tracker 600 ATVs Recalled for Crash Hazard

    Textron Specialized Vehicles is recalling about 1,750 Arctic Cat Alterra 600 and Tracker 600 ATVs because a fuse in the electrical system can fail during operation, causing sudden loss of engine power and headlights, which poses a crash hazard.

    Product
    Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2022·2022-07-13

    Siemens X-ray System Fan Wear May Cause Equipment Malfunction

    Siemens is recalling 88 Artis Icono X-ray systems in the U.S. due to increased fan wear that could lead to electrical failure and malfunction of the imaging system during operation.

    Product
    Artis Icono, Interventional Fluoroscopic X-Ray System, Model No. 11327600
    Category
    Medical Device
    Distribution
    32 states
  • HighFDA (Devices)·Z-1135-2022·2022-06-01

    Medical beds with motorized wheels face uncontrolled motion risk

    Umano Medical recalls 228 adjustable hospital beds due to potential electrical system failure that could cause uncontrolled movement of the motorized wheel system.

    Product
    AC-powered adjustable medical beds with built-in electric DC actuators and controls.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0935-2022·2022-04-20

    ECG Electrode Set Fails Electrical Safety, May Prevent Effective Defibrillation

    Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.

    Product
    CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V241000·2022-04-13

    New England Wheels Recalls 2021-2022 Frontrunner Buses for Fire Risk

    New England Wheels is recalling 2021-2022 Frontrunner buses because a faulty module may cause a fire. Owners should contact the manufacturer for a free repair.

    Product
    NEW ENGLAND WHEELS — NEW ENGLAND WHEELS FRONTRUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V122000·2022-03-03

    Kawasaki Recalls W800 Motorcycles Due to Horn Harness Defect

    Kawasaki is recalling 2019-2022 W800 motorcycles because the horn harness may break, rendering the horn inoperable and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI W800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00N000·2021-12-29

    Kenworth and Peterbilt Commercial Trucks Recalled for Methane Detection System Failure

    PACCAR is recalling approximately 1,107 Kenworth and Peterbilt commercial trucks (2016–2022) due to methane detection system power loss. If the system loses electrical power, operators may not detect dangerous methane levels, increasing fire and injury risk.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, T880, 567, 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V867000·2021-11-08

    Hazard Lights Disabled When Ignition Off in Autocar Xpeditor Vehicles

    Autocar is recalling 2019-2022 Xpeditor vehicles because the hazard lights will not function with the ignition turned off. This violates federal safety standards and could increase crash risk in hazard situations.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V748000·2021-09-24

    MCI Motorcoaches Recalled for Main Distribution Panel Fire Risk

    Motor Coach Industries is recalling specific 2017-2021 motorcoaches because a circuit board in the battery compartment may fail, potentially causing a fire or unexpected shutdown.

    Product
    MCI — MCI D45 CRT LE, D4000ISTV, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V403000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Water Intrusion Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V356000·2021-05-14

    Motorhome Recall: Faulty Generator Regulator in 2020-2021 Roadtrek Models

    Roadtrek is recalling 2020-2021 Zion and Play motorhomes due to a faulty generator regulator that may damage the battery and cause electrical system failure. This creates a risk of injury from battery cap detachment or acid spill.

    Product
    ROADTREK — ROADTREK ZION SRT, PLAY, ZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1313-2021·2021-04-07

    Medtronic Bio-Console 560 Blood Pumping Console Recalled for Electrical Failure

    Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.

    Product
    Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1, R560BCS1. Used in cardiopulmonary bypass (CPB) procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide