Hazard Type

Electrical Hazard Recalls

804 product recalls involving electrical hazard. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.

804Total Recalls
54Critical
37.0MUnits Affected
All Recalls

Every Electrical Hazard Recall

Sorted by most recent. Click any recall for full details and safety information.

804 recalls
RecallCPSC
Online At Www.lusbrands.com From November 2019 Through February 2020 For Between $125 And $144.
LUS Recalls Hair Dryers Due to Electrocution or Shock Hazard (Recall Alert)
Appliances·2,700 affected·Apr 23, 2020
High RiskFDA
Siemens Medical Solutions Usa, Inc
Siemens Cios Alpha VA30-mobile X-Ray system, Material # 11105200 The Cios Alpha and Cios Spin are a mobile X-Ray system designed to pro...
Medical Devices·16 affected·Apr 20, 2020
High RiskFDA
Siemens Medical Solutions Usa, Inc
Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Cios Alpha and Cios Spin are a mobile X-Ray system designed to prov...
Medical Devices·4 affected·Apr 20, 2020
High RiskFDA
Philips North America, Llc
Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are an accessory to the compatible monitor/defibrillator Switch...
Cardiac Devices·21,683 affected·Apr 20, 2020
High RiskFDA
Siemens Medical Solutions Usa, Inc
Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Medical Devices·20 affected·Apr 17, 2020
High RiskFDA
Philips North America, Llc
Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product Usage: is for use in the hospital by qualified medical person...
Cardiac Devices·94,034 affected·Apr 13, 2020
High RiskFDA
Philips North America, Llc
Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnost...
Surgical Devices·25 affected·Apr 10, 2020
High RiskFDA
Philips North America, Llc
Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnost...
Surgical Devices·25 affected·Apr 10, 2020
High RiskFDA
Beckman Coulter Inc.
iChem¿VELOCITY Urine Chemistry System-
Medical Devices·1,557 affected·Mar 30, 2020
High RiskFDA
Physio-control, Inc.
LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/, U3011790-XXX - Product Usage: The L...
Cardiac Devices·173,459 affected·Mar 20, 2020
High RiskFDA
Welch Allyn, Inc/mortara
X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM I...
Medical Devices·78,521 affected·Mar 18, 2020
High RiskFDA
Welch Allyn, Inc/mortara
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI 280, ELI 380, R-Sc...
Diagnostic Devices·78,521 affected·Mar 18, 2020
High RiskFDA
Welch Allyn, Inc/mortara
Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor under the following device names: PAT CBL 10WIRE AHA SNAP JSCREW, PAT ...
Medical Devices·78,521 affected·Mar 18, 2020
High RiskFDA
Welch Allyn, Inc/mortara
Replaceable lead set for the Wireless Acquisition Module (WAM), which is the ECG front-end for various Electrocardiographs. Sold under ...
Medical Devices·78,521 affected·Mar 18, 2020
High RiskFDA
Welch Allyn, Inc/mortara
T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF transmission of simultaneous 12-le...
Diagnostic Devices·78,521 affected·Mar 18, 2020
High RiskFDA
Welch Allyn, Inc/mortara
Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisition and editing system.
Cardiac Devices·78,521 affected·Mar 18, 2020
CriticalFDA
Sysmex America, Inc.
Sysmex CV-11 Sample Unit, an integrated modular sampler that conveys specimens to either the UF-5000 or UD-10 analyzers.
Medical Devices·40 affected·Jan 21, 2020
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
Cardiac Devices·29,952 affected·Dec 20, 2019
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
Cardiac Devices·705 affected·Dec 20, 2019
RecallCPSC
Online At Www.skylightframe.com And Amazon.com, And In Von Maur Stores Nationwide From April 2018 Through March 2019 For About $160 With The Digital Photo Frame.
Skylight Recalls Power Adapters Sold with Digital Photo Frames Due to Electrical Shock Hazard (Recall Alert)
Consumer Products·65,000 affected·Nov 7, 2019
High RiskFDA
Philips North America, Llc
HeartStart XL+ Defibrillator/Monitor, Model 861290
Cardiac Devices·23,749 affected·Oct 16, 2019
High RiskFDA
Mizuho Osi
Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used ...
Medical Devices·174 affected·Oct 14, 2019
High RiskFDA
Lifelines Neuro Company
ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system ElectroTek is intended...
Diagnostic Devices·8 affected·Oct 11, 2019
High RiskFDA
Lifelines Neuro Company
ElectroTek Temporal Sensor Cable Gold - Long Length, Single Length - Product Usage: The electroencephalographic system ElectroTek is inte...
Diagnostic Devices·12 affected·Oct 11, 2019
RecallCPSC
Viqua Distributors And Plumbing Contractors Nationwide From May 2018 Through October 2019 For Between About $460 And $500 For The Valve Kit.
VIQUA Recalls Solenoid Valve Kits for UV Water Treatment Systems Due to Electrical Shock Hazard
Consumer Products·70 affected·Oct 3, 2019
High RiskFDA
Baxter Healthcare Corporation
TherMax Blood Warmer Unit
Medical Devices·504 affected·Sep 19, 2019
High RiskFDA
Boston Scientific Corporation
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator
Medical Implants·404 affected·Aug 21, 2019
High RiskFDA
Boston Scientific Corporation
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Medical Implants·28 affected·Aug 21, 2019
RecallCPSC
Crate & Barrel And Home Appliance Stores Nationwide And Online At Amazon.com And Other Websites From September 2018 Through June 2019 For Between $24 And $44.
Bodum Recalls Toasters Due to Shock Hazard
Consumer Products·2,400 affected·Jul 17, 2019
High RiskFDA
Philips North America, Llc
HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable external defibrillato...
Cardiac Devices·2 affected·Jul 16, 2019
RecallCPSC
Office Depot Stores In The United States And Puerto Rico And Online At Officedepot.com From April 1, 2017 Through February 22, 2019 For About $500.
Office Depot Recalls Desks Due To Shock Hazard (Recall Alert)
Furniture·19,000 affected·Jul 10, 2019
High RiskFDA
Capso Vision, Inc.
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The Caps...
Medical Devices·44 affected·Jul 3, 2019
RecallCPSC
Lighting Store Showrooms Nationwide And Online E-commerce Retailers Where Ceiling Fans Are Sold From November 2017 Through May 2019 For Between $150 And $300.
Hunter Fan Recalls Brunswick Three and Four Light Ceiling Fans Due to Shock Hazard
Heating & Cooling·7,800 affected·Jun 20, 2019
CriticalFDA
St Jude Medical Inc.
ELLIPSE VR, REF: CD1377-36QC Implantable cardioverter defibrillators (ICDs)
Medical Implants·47 affected·Jun 20, 2019
CriticalFDA
St Jude Medical Inc.
ELLIPSE DR, REF: CD2377-36QC Implantable cardioverter defibrillators (ICDs)
Medical Implants·21 affected·Jun 20, 2019
CriticalFDA
St Jude Medical Inc.
ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36C, UDI: 05414734507585
Cardiac Devices·15 affected·Jun 20, 2019
High RiskFDA
Philips North America, Llc
Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536...
Cardiac Devices·97,794 affected·Jun 7, 2019
Medium RiskCPSC
Apple Stores And Other Home Electronics Stores Nationwide, And Online At Apple.com From January 2003 Through January 2015 For About $30.
Apple Recalls Three-Prong Wall Plug Adapters Included in World Travel Adapter Kit Due to Risk of Electric Shock
Consumer Products·814,000 affected·Jun 5, 2019
RecallCPSC
Independent Lighting Retailers Nationwide And Online At Build.com, Circa Lighting, Lightology, Lumens, Wayfair, And Y Lighting From January 2013 Through December 2018 For Between $385 And $525.
Generation Brands Recalls Glass Pendant Light Fixtures Due to Risk of Injury
Consumer Products·1,200 affected·Jun 4, 2019
High RiskFDA
Gn Otometrics
The ICS CHARTR EP 200
Medical Devices·3,071 affected·May 28, 2019
High RiskFDA
Abbott Gmbh & Co. Kg
The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity ci-series Control Modul...
Diagnostic Devices·943 affected·May 21, 2019
High RiskFDA
Maquet Cardiovascular Us Sales, Llc
GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 ...
Surgical Devices·163 affected·May 6, 2019
High RiskFDA
Boston Scientific Neuromodulation Corporation
LinearTM 3-4 50 cm 8 Contact Lead Kit, part number M365SC2352500. Leads function as a component of Boston Scientific's Spinal Cord Stim...
Medical Devices·3 affected·Apr 24, 2019
High RiskFDA
Coopersurgical, Inc.
LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V combines three compo...
Surgical Devices·19 affected·Apr 23, 2019
High RiskFDA
Ad-tech Medical Instrument Corporation
AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale Depth Electrodes, ...
Medical Devices·18 affected·Apr 16, 2019
RecallCPSC
Authorized Specialized Retailers Nationwide From July 2016 Through January 2019 For Between $1,650 And $11,500.
Specialized Recalls Bicycles with Steerer Tube Collars Due to Fall and Injury Hazards
Bicycles & Wheeled Sports·63,000 affected·Apr 11, 2019
RecallFDA
Advanced Bionics, Llc
SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical SoundWave Professional Su...
Medical Implants·364 affected·Apr 4, 2019
High RiskFDA
Philips Medical Systems Nederlands
Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for ...
Diagnostic Devices·4 affected·Mar 25, 2019