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
High RiskFDA
Spacelabs Healthcare, Inc.
Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software Version: N/A P...
Medical Devices57 affectedMar 26, 2026
RecallCPSC
Online At Thekiddospacestore.com From November 2023 Through February 2025 For Between $13 And $40.
TheKiddoSpace Recalls Children's Christmas Tree Play Sets Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban and Mandatory Standard for Toys
Toys300 affectedFeb 26, 2026
High RiskFDA
Olympus Corporation Of The Americas
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product Description: ...
Surgical Devices93 affectedFeb 25, 2026
High RiskFDA
Olympus Corporation Of The Americas
Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Desc...
Surgical Devices7 affectedFeb 25, 2026
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD10F; Model Number: 722002;
Medical Devices12 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD10/10; Model Number: 722027;
Medical Devices22 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD20; Model Number: 722028;
Medical Devices2 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Product Name: Allura Xper FD10C; Model number: 722001;
Medical Devices38 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD10; Model Number: 722003;
Medical Devices93 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD10/10; Model Number: 722011;
Medical Devices21 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD20/20; Model Number: 722038;
Medical Devices8 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD10/10; Model Number: 722005;
Medical Devices14 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD20; Model Number: 722012;
Medical Devices79 affectedDec 15, 2025
High RiskFDA
Philips Medical Systems Nederland B.v.
Allura Xper FD20/10; Model Number: 722029;
Medical Devices4 affectedDec 15, 2025
High RiskFDA
Steris Corporation
AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended fo...
Surgical Devices10 affectedNov 19, 2025
High RiskFDA
Steris Corporation
AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended f...
Surgical Devices22 affectedNov 19, 2025
RecallCPSC
Various Distributors Nationwide From July 2024 Through December 2024 For Between $6,000 And $12,000.
Sauna360 Recalls Tylö Halmstad and Kiruna Hybrid Saunas Due to Fall Hazard
Consumer Products1,000 affectedOct 23, 2025
RecallFDA
Datascope Corp.
Cardiosave Rescue
Medical Devices47 affectedOct 23, 2025
RecallFDA
Datascope Corp.
Cardiosave Hybrid
Medical Devices11,470 affectedOct 23, 2025
High RiskFDA
Canon Medical System, Usa, Inc.
VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7.
Medical Devices2 affectedOct 16, 2025
High RiskFDA
Thoratec Llc
Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Model/Catalog Number: 106015, HeartMate II¿ LVAS Kit, with Pocket Co...
Medical Implants248 affectedOct 9, 2025
CriticalFDA
Max Mobility Llc
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Ass...
Medical Devices8,413 affectedAug 12, 2025
CriticalFDA
Max Mobility Llc
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assis...
Medical Devices25,389 affectedAug 12, 2025
CriticalFDA
Max Mobility Llc
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assi...
Medical Devices15,834 affectedAug 12, 2025
CriticalFDA
Mo-vis Bvba
IDM-MICRO-R. Electrical wheelchair component.
Medical Devices15 affectedJul 10, 2025
CriticalFDA
Mo-vis Bvba
Micro Joystick R-net. Electrical wheelchair component.
Medical Devices3 affectedJul 10, 2025
RecallCPSC
Harbor Freight Tools Stores Nationwide From February 2025 Through April 2025 For About $950.
Harbor Freight Tools Recalls Predator 2000-Watt Power Stations Due to Shock Hazard
Tools6,500 affectedJul 3, 2025
CriticalFDA
Thoratec Llc
Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A Product Descr...
Medical Implants53 affectedJun 23, 2025
High RiskFDA
Medtronic, Inc.
Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Azur...
Medical Devices3,909 affectedJun 17, 2025
High RiskFDA
Medtronic, Inc.
Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following software components: ...
Medical Devices5,418 affectedJun 17, 2025
RecallCPSC
Dealers And Distributors Of Audiovisual (av) Equipment And Electrical Supplies Nationwide From September 2024 Through April 2025 For About $300 For The Power Interfaces, And Between $1,250 And $1,400 For The Lumaris Ledtape Light Starter Kits And The Homeworks Systems.
Lutron Recalls Power Interfaces for LED Tape Lights Due to Shock Hazard
Consumer Products1,944 affectedJun 5, 2025
RecallFDA
Lumithera Inc
Brand Name: Valeda Light Delivery System Product Name: Light Based Device for Dry Age Related Macular Degeneration Product Description:...
Medical Devices8 affectedMay 7, 2025
CriticalFDA
Thoratec Llc
HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with HeartMate 3 and II Le...
Cardiac Devices1,661 affectedMar 13, 2025
RecallCPSC
Lighting Showrooms Nationwide And Online At Amazon.com And Lowes.com From June 2023 Through December 2024 For Between $165 And $240.
Kichler Lighting Recalls Wall Sconces Due to Risk of Electric Shock
Lighting2,760 affectedFeb 27, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Description: The Powerhe...
Cardiac Devices7,221 affectedFeb 13, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C,...
Cardiac Devices960 affectedFeb 13, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Ve...
Cardiac Devices73 affectedFeb 13, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-...
Cardiac Devices1,312 affectedFeb 13, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4) G5A-03A, (5) G5A-19A,...
Cardiac Devices2,268 affectedFeb 13, 2025
High RiskFDA
Zoll Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version: NA Product Des...
Cardiac Devices56,981 affectedFeb 13, 2025
RecallCPSC
Online At Aliexpress.com From May 2023 Through November 2024 For Between $41 And $135.
AliExpress Recalls Multi Styler Hair Dryers Due to Electrocution or Shock Hazards; Sold on AliExpress.com
Appliances980 affectedJan 30, 2025
RecallCPSC
Online At Shein.com From July 2024 Through October 2024 For Between $9 And $21.
SHEIN Distribution Corporation Recalls Teckwe Hair Dryer Brushes Due to Electrocution or Shock Hazard
Appliances310 affectedJan 23, 2025
High RiskFDA
Coopersurgical, Inc.
Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An ele...
Respiratory Devices37 affectedNov 15, 2024
High RiskFDA
Coopersurgical, Inc.
Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23054 Software Version: N/A Product Description: An elec...
Respiratory Devices22 affectedNov 15, 2024
High RiskFDA
Coopersurgical, Inc.
Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unknown Software Version: N/A Product Description...
Respiratory Devices34 affectedNov 15, 2024
High RiskFDA
Defibtech, Llc
Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DD...
Cardiac Devices22,294 affectedOct 14, 2024
RecallCPSC
Graybar Electric Co., Of St Louis, Missouri; Keystone Automotive Operations Inc., Of Exeter, Pennsylvania; Hamilton Manufacturing Corp., Of Holland, Ohio; And Controlled Access Of The Midwest, Of Pleasant Hill, Iowa, And Online At Comfortsolutions.caframobrands.com And Amazon.com From October 2023 Through May 2024 For About $150.
Caframo Cabinet Heaters Recalled Due to Electrocution Hazard; Manufactured by Caframo Limited
Furniture2,140 affectedSep 19, 2024
High RiskFDA
Baxter Healthcare Corporation
Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
Medical Devices0 affectedSep 19, 2024