The Recall Desk

Hazard

Electric Shock recalls

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

What the numbers show

Total
378
Critical
17
Severe
62
Most recent
2026-08-13

Of the 378 electric shock recalls we have scored against our rubric, 17 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 62 (16%) 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 electric 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.

76–100 of 378

  • HighFDA (Devices)·Z-3024-2017·2017-08-23

    GE Optima MR450w 1.5T MRI Scanner Recalled for Potential Shock Hazard

    GE Medical Systems is recalling 68 Optima MR450w 1.5T MRI scanners due to possible incorrect wiring in the Uninterruptable Power Supply, which could create a shock hazard.

    Product
    Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17201·2017-08-08

    NVIDIA Recalls European Plug Heads for Power Adaptors Due to Shock Hazard

    NVIDIA is recalling European plug heads for SHIELD power adaptors because they can break and expose metal prongs, posing an electric shock hazard.

    Product
    European plug heads for NVIDIA SHIELD™ power adaptors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2685-2017·2017-07-12

    PerkinElmer Multiphor II Electrophoresis System Recalled for Electric Shock Risk

    PerkinElmer is recalling 241 Multiphor II Electrophoresis Systems due to a potential electric shock hazard if grommets are not installed.

    Product
    Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D elect
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·17159·2017-05-19

    Blomberg and Summit Electric Ranges Recalled for Electrocution Hazard

    Arçelik A.S. is recalling about 6,300 Blomberg and Summit electric ranges because they can become energized, posing shock and electrocution risks.

    Product
    Blomberg and Summit electric ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17130·2017-04-12

    Customatic Recalls Adjustable Beds Due to Electric Shock Hazard

    Customatic Beds is recalling about 50,000 adjustable bed bases because side-mounted AC outlets may be incorrectly wired, posing an electric shock hazard.

    Product
    Adjustable beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0865-2017·2016-12-28

    Accuray Recalls CyberKnife Robotic Radiosurgery Systems Due to Electric Shock Risk

    Accuray is recalling 115 CyberKnife Robotic Radiosurgery Systems (models G3, G4, VSI) due to a potential electric shock hazard during maintenance.

    Product
    CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body
    Category
    Medical Device
    Distribution
    25 states
  • ModerateFDA (Devices)·Z-0825-2017·2016-12-28

    Philips Ingenia MR-OR Recalled for Potential Touch Current Exposure

    Philips is recalling nine Ingenia MR-OR units due to a possibility that patients or users may be exposed to a very small level of touch current.

    Product
    Ingenia MR-OR; 781437, 781438 The MR-OR option is intended for allowing transfer of a neurosurgical patient from OR suite to MR suite and back with tools and instructions for proper positioning and MR imaging of those patients. MR-OR option also facilitates execution of simple n
    Category
    Medical Device
    Distribution
    2 states
  • SevereCPSC·17017·2016-10-18

    3 Squares Rice and Slow Cookers Recalled for Fire and Shock Hazards

    Sherwood Marketing is recalling 3 Squares rice and slow cookers because improperly installed wiring can cause electrical shorting, posing fire and electric shock risks.

    Product
    3 Squares rice and slow cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V710000·2016-10-05

    Altec Recalls 2014-2015 Aerial Devices Due to Boom Tip Cover Defect

    Altec is recalling 219 model year 2014-2015 aerial devices because an improperly sized boom tip cover opening may allow contact with energized conductors, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2769-2016·2016-09-14

    Innovision Innocor Cardiopulmonary Testing System Recalled for Electric Shock Risk

    Innovision A/S is recalling eight Innocor Cardiopulmonary Exercise and Lung Function Testing Systems to replace USB cables that lack galvanic isolation, preventing potential electric shock.

    Product
    Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diagnostic device that measures or calculates a number of hemodynamic and metabolic parameters.
    Category
    Medical Device
    Distribution
    2 states
  • HighCPSC·16224·2016-07-14

    Home Source Recalls Floor Lamps Due to Fire and Shock Hazards

    Home Source is recalling about 2,700 floor lamps sold in the New York area and online because defective sockets can cause fires and electric shocks.

    Product
    Floor lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16201·2016-06-23

    3M Recalls Vented Hard Hats Due to Electric Shock Hazard

    3M is recalling about 7,500 vented hard hats sold online because they do not provide the advertised protection against electric shock.

    Product
    Vented hard hats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1081-2016·2016-03-16

    Stryker Position Pro Mattress Recalled for Power Cord Fire Risk

    Stryker is recalling Position Pro Mattresses because the power cord may melt, posing risks of electric shock and fire.

    Product
    Stryker Position Pro Mattress. Mattress, Air Flotation, Alternating Pressure. PositionPRO is a powered pressure relief support surface with low air loss (LAL) intended for medical purposes. PositionPRO consists of multiple air cells filled and emptied by an integrated contro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16111·2016-03-01

    United Pet Group Recalls Top Fin Aquarium Power Filters for Shock Hazard

    United Pet Group is recalling Top Fin power filters for aquariums because a conductor can expose consumers to electric shock. No injuries have been reported.

    Product
    Top Fin™ Power Filters for Aquariums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16106·2016-02-18

    Apple Recalls Travel Adapter Kits Due to Electric Shock Risk

    Apple is recalling approximately 814,000 travel adapter kits and plug adapters because the two-prong adapters can break and expose metal, posing an electric shock risk.

    Product
    AC adapter kits and plug adapters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16724·2016-01-27

    Lunera Recalls Helen GX23 LED Lamps Due to Fire and Shock Hazards

    Lunera is recalling approximately 60,000 Helen GX23 LED lamps because they can overheat, posing fire, burn, and electric shock hazards. No injuries have been reported.

    Product
    Helen GX23 LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16054·2015-12-08

    TCP and Great Value LED Lamps Recalled for Electrical Shock Hazard

    Technical Consumer Products is recalling specific 14-watt LED PAR38 lamps sold at Walmart and electrical distributors due to a risk of electric shock in wet locations.

    Product
    Technical Consumer Products (TCP) and Great Value LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide