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.

101–125 of 378

  • SevereFDA (Devices)·Z-0169-2016·2015-11-04

    Welch Allyn KleenSpec Corded Illuminator Recalled for Electric Shock Risk

    Welch Allyn is recalling KleenSpec Corded Illuminators because they may be connected to AC power, posing a shock hazard.

    Product
    Welch Allyn KleenSpec Corded Illumination System, Vaginal Speculum Lighting System, Model Number 78x Series Illuminator, REF 901070, Catalog Numbers 78800, 73410, 73412, 73414, 73416, 78810, 78812, 78814 and 78816, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15754·2015-09-15

    Segway Recalls Off-Board Chargers for Personal Transporters Due to Shock Hazard

    Segway is recalling approximately 17 off-board chargers for its Personal Transporters because a wire can detach and cause an electric shock. No injuries have been reported.

    Product
    Off-Board Charger for Segway Personal Transporter (PT)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15186·2015-07-15

    Olympus Recalls VG 170 Digital Cameras Due to Electric Shock Hazard

    Olympus is recalling about 1,200 VG 170 digital cameras sold at HHGregg because an improperly installed part poses an electric shock risk. No injuries have been reported.

    Product
    Olympus VG 170 Digital Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15120·2015-04-22

    Shark Vacuum Cleaners Recalled by Euro-Pro Due to Shock Hazard

    Euro-Pro is recalling Shark vacuum cleaners because the aluminum wand can disconnect and remain energized, posing an electric shock risk.

    Product
    Shark Powered Rotator Lift-Away vacuum cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1250-2015·2015-03-18

    Pivotal Health Solutions Recalls Apollo Laser Desktop Control Units

    Pivotal Health Solutions is recalling 35 Apollo Laser Desktop Control Units because internal mounting kits do not meet safety standards, increasing the risk of electric shock.

    Product
    Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and st
    Category
    Medical Device
    Distribution
    17 states
  • SevereCPSC·15024·2014-11-13

    Ventamatic Recalls Cool Draft Misting Fans Due to Fire and Shock Risk

    Ventamatic is recalling about 450 Cool Draft misting fans because improper wiring creates fire and electric shock hazards. Consumers should stop using the fans immediately.

    Product
    Cool Draft Misting Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0081-2015·2014-10-22

    Siemens Clinitek Status+ Power Supply Adapters Recalled for Electric Shock Risk

    Siemens Healthcare Diagnostics is recalling approximately 4,200 external power supply adapters for the Clinitek Status+ urine analyzer due to damage that can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status+ The Clinitek Status systems is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0082-2015·2014-10-22

    Siemens Clinitek Status Power Supply Adaptors Recalled for Shock Risk

    Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer due to damage that can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status Connect System The Clinitek Status system is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2015·2014-10-22

    Siemens Clinitek Status Power Supply Adaptors Recalled for Electric Shock Risk

    Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer because they are damaged and can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status Power Supply Adaptor - Spare Part The Clinitek Status system is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14260·2014-08-21

    SolarWorld Recalls Solar Systems with Copper Grounding Lugs

    SolarWorld is recalling solar systems installed with bare-copper grounding lugs due to corrosion risks that could cause electric shock, electrocution, or fire.

    Product
    SolarWorld Solar Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14233·2014-07-17

    Popkiller Recalls USB Chargers and Cables Due to Fire and Shock Hazards

    Popkiller is recalling USB car chargers, power adapters, and cables due to fire and electric shock risks. No injuries have been reported.

    Product
    USB car charger adapters, power adapters and 8-pin charger cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1716-2014·2014-06-11

    Stryker NAV3i Platform Power Box Recalled for Missing Electrical Insulation

    Stryker is recalling 20 NAV3i Platform Power Boxes that may lack electrical insulation on soldering joints, posing a risk of electric shock.

    Product
    The NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera, SPC-3 Computer, IO-Tablet (touch screen) and the monitor).
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-1336-2014·2014-04-16

    Playtex Electric Breast Pump Recall Due to Power Adapter Shock Risk

    Energizer Personal Care is recalling Playtex Deluxe Double Electric Breast Pumps because loose power adapter casings may cause electric shock.

    Product
    Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14134·2014-03-18

    Schneider Electric Recalls Square D Circuit Breakers Due to Fire Hazard

    Schneider Electric is recalling specific Square D F and K frame circuit breakers because they may fail to trip during overloads, posing fire, burn, and shock risks.

    Product
    Square D branded, molded case F and K frame circuit breakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0838-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 2 units of the Aquarius Hot/Cold Therapy Combo Unit due to temperature monitoring failures and electric shock reports.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Shoulder Blanket w/ Straps NS, REF T655NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0837-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature and Shock Risks

    DeRoyal Industries is recalling 48 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature and have caused electric shocks.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Knee Blanket w/ Straps NS, REF T654NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0835-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 121 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Knee/Shoulder Blanket NS, REF T652NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0836-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 409 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Knee/Shoulder Blnkt NS, REF T653NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0834-2014·2014-02-05

    DeRoyal Aquarius Temperature Therapy Units Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 738 Aquarius Temperature Therapy units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.

    Product
    Aquarius (TM) TEMPERATURE THERAPY, REF T650, Rx Only, Manufactured for DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849, Made in China. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0839-2014·2014-02-05

    DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure

    DeRoyal Industries is recalling 25 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.

    Product
    DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Foot/Ankle Blanket NS, REF T656NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V230000·2013-05-31

    Ford Recalls 2013 Lincoln MKZ Vehicles for Engine Block Heater Defect

    Ford is recalling 2013 Lincoln MKZ vehicles equipped with engine block heaters because the cord insulation may crack, exposing wires and increasing the risk of electric shock.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide