The Recall Desk

Hazard

Electrical Shock recalls

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

What the numbers show

Total
325
Critical
2
Severe
58
Most recent
2026-08-26

Of the 325 electrical shock recalls we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 58 (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 electrical shock 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.

226–250 of 325

  • HighCPSC·14738·2014-06-26

    Roland Recalls RD-800 Digital Pianos Due to Electrical Shock Hazard

    Roland is recalling approximately 640 RD-800 digital pianos because the AC power cord can be connected to XLR output jacks, posing an electrical shock hazard.

    Product
    Digital Electric Piano
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1733-2014·2014-06-18

    Siemens Vista Air Compressor Recalled for Fire and Shock Hazards

    Siemens Healthcare Diagnostics is recalling four Vista Air Compressors because miswiring could cause a fire or electrical shock if powered up.

    Product
    Siemens Healthcare Diagnostics Vista Air Compressor. Vista AirCompressor replacement part: SMN 10706557 SKIT Air Compressor Assy, used on the Dimension Vista 500 and Dimension Vista 1500 systems. Siemens Healthcare Diagnostics Dimension Vista System is an in vitro diagnos
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1715-2014·2014-06-11

    Stryker NAV3i Platform Power Boxes Recalled for Missing Electrical Insulation

    Stryker is recalling 20 NAV3i Platform Power Boxes because they may lack electrical insulation on soldering joints, posing a shock hazard.

    Product
    The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera, SPC-3 Computer and IO-Tablet (touch screen) as well as the monitor, articulated arms and cart housing. This Navigation system is used in combination with surgical
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0905-2014·2014-02-12

    Medtronic Aquamantys3 Pump Generator Recalled for Electrical Safety Defect

    Medtronic is recalling 242 Aquamantys3 Pump Generators because internal protection circuitry may fail, exposing patients to DC voltage during surgery.

    Product
    Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as shipped, including accessories) The Aquamantys3 System combines radio frequency (RF) energy and saline to reduce blood loss during and after surgical procedur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14009·2013-10-30

    HeathCo Recalls Motion-Activated Outdoor Lights Due to Electrical Shock Hazard

    HeathCo is recalling about 223,000 motion-activated outdoor lights in the U.S. and Canada because the internal wiring can energize the fixture surface, posing an electrical shock hazard.

    Product
    Motion-Activated Outdoor Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0008-2014·2013-10-16

    Draeger Fabius Anesthesia Machines Recalled for Electrical Clearance Defects

    Draeger Medical is recalling 1,127 Fabius anesthesia machines worldwide because some units failed high-voltage tests and did not maintain minimum electrical clearance.

    Product
    Draeger Fabius GS Premium, Fabius OS, Fabius Tiro, Fabius Tiro D-M Product Usage: used to administer anesthesia and ventilation to patients during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2097-2013·2013-09-04

    Megadyne Recalls E-Z Clean Laparoscopic Electrodes Due to Insulation Breach

    Megadyne Medical Products is recalling specific lots of E-Z Clean Disposable Laparoscopic Electrodes due to potential insulation breaches.

    Product
    E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS. Expiration dates of 05/2018 to 07/2018. Sterile. RX ONLY. This product is packaged individually in a chevron Tyvek¿ - polyester peel pouch, 6 pouches per box. The E-Z Clean laparoscopic electrode is
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·13V378000·2013-08-21

    Altec Recalls Aerial Devices Due to Electrical Shock Risk

    Altec is recalling 2005-2013 AH75, AH85, and AH100 aerial devices because a cable may breach insulation, increasing the risk of electrical shock to operators.

    Product
    ALTEC — ALTEC AH100, AH75, AH85
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1123-2013·2013-04-24

    Advanced Sterilization Products Recalls EVOTECH Endoscope Cleaner Systems

    Advanced Sterilization Products is recalling 273 EVOTECH Endoscope Cleaner & Reprocessor Systems because they did not receive sufficient High Potential (HIPOT) DC voltage testing.

    Product
    EVOTECH Endoscope Cleaner & 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·13V088000·2013-03-12

    Terex Recalls 2012 Aerial Devices Due to Electrical Shock Risk

    Terex is recalling 2012 T292, TL, and NT Aerial Devices because a faulty inverter may fail to provide ground fault protection, posing an electrocution risk.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13130·2013-03-05

    Tween Brands Recalls Disco Lights Due to Electrical Shock Hazard

    Tween Brands is recalling Style My Room by Justice Disco Lights because accessible wiring and overheating pose an electrical shock risk.

    Product
    Style my Room by Justice Disco Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0818-2013·2013-02-20

    Richmar Foam Electrodes Recalled for Terminal Separation Defect

    NAImco Inc dba Richmar Inc is recalling foam electrodes where the socket terminal may pull away from the lead wire. The defect poses a risk of electrical shock or injury.

    Product
    Foam electrodes with Silver-Carbon construction: P/N 202-9271, Cat No. 400-898, 2" x 2" Electrode, Foam, AG, All Serial Numbers distributed between 11/01/2009 and 01/31/2010 P/N 202-9281, Cat No. 202-9281, 2" Round Electrode, Foam, AG, All Serial Numb
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0287-2013·2012-11-21

    Dako PT Link Waterbath Recalled for Electrical Shock Hazard

    Dako North America Inc. is recalling 136 PT Link Waterbath units due to a potential electrical shock hazard if the heater pad becomes wet.

    Product
    PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0022-2013·2012-10-17

    3M Recalls Steri-Vac Gas Sterilizers Due to Electrical Grounding Defect

    3M is recalling Steri-Vac 5XL and 8XL gas sterilizers because the electrical grounding mechanism did not meet safety standards.

    Product
    3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed to sterilize heat- and/or moisture-sensitive devices. This gas sterilizer/aerator is intended for indoor use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·12743·2012-08-16

    World Class Recalls Pet Heating Mats Due to Fire and Shock Hazards

    World Class Inc. is recalling indoor pet heating mats sold on Amazon.com due to poor wiring that poses fire and electrical shock risks.

    Product
    Indoor Pet Heating Comfort Pad Mats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12115·2012-02-22

    Meijer Recalls Touch Point Fan Heaters Due to Fire and Shock Hazards

    Meijer is recalling Touch Point fan heaters because exposed electrical components can cause overheating, fire, and electrical shock. Consumers should stop using the units and return them for a refund.

    Product
    Forced Air Heater
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12046·2011-11-22

    HeathCo Recalls Motion Sensing Wall Switches Due to Electrical Shock Hazard

    HeathCo is recalling approximately 75,000 motion sensing wall switches due to a risk of electrical shock. Consumers should stop using the switches and contact the company for a free replacement.

    Product
    Heath®/Zenith and WirelessCommand® motion sensing wall switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·12703·2011-11-10

    Wolfgang Puck Electric Grills Recalled for Overheating and Shock Hazards

    W.P. Appliances is recalling Wolfgang Puck electric grills/griddles sold at HSN due to electrical wiring defects that pose risks of overheating and electrical shock.

    Product
    Wolfgang Puck Electric Reversible Tri-Grill/Griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12008·2011-10-11

    Nidec Recalls Ecotech Pool Pump Motors Due to Electrical Shock Hazard

    Nidec Motor Corporation is recalling approximately 2,000 Ecotech EZ Variable Speed pool pump motors because the pump cover is not properly grounded, posing an electrical shock hazard.

    Product
    Ecotech EZ® Variable Speed pool pump motors
    Category
    Consumer Product
    Distribution
    Distributed nationwide