The Recall Desk

Hazard

Crush Injury recalls

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

What the numbers show

Total
87
Critical
11
Severe
24
Most recent
2026-06-18

Of the 87 crush injury recalls we have scored against our rubric, 11 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 24 (28%) 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 crush injury 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.

26–50 of 87

  • HighFDA (Devices)·Z-2279-2023·2023-08-09

    Image intensifier detachment hazard in OEC fluoroscopy imaging systems

    GE OEC field upgrade kits for fluoroscopy systems may have image intensifiers that detach during movement, potentially falling and causing injuries.

    Product
    Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER, 9 INCH, TOSHIBA; P/N 5761613 SERVICE PART, IMAGE INTENSIFIER, 9 INCH - used with OEC Flexiview 8800, OEC 9800, and OEC 9900 Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1383-2023·2023-04-19

    X-ray imaging system ceiling suspension may descend without adequate maintenance

    Philips DigitalDiagnost C50 ceiling suspensions may descend unexpectedly if annual preventive maintenance is not performed, potentially injuring patients and healthcare workers.

    Product
    DigitalDiagnost C50 1.1-intended for use in generating radiographic images of human anatomy Model Number : 712204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·23177·2023-04-13

    Luxor Audiovisual Carts Recalled for Tip-Over Hazard; Three Deaths Reported

    Luxor Workspaces is recalling approximately 84,700 audiovisual carts that can tip over when loaded with heavy objects like cathode-ray tube televisions. Three children have died and one was seriously injured in tip-over incidents between 2006 and 2016.

    Product
    Luxor A/V carts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V236000·2023-03-31

    2022 and 2023 Kia Carnival power sliding doors auto-reverse failure

    Kia is recalling 2022 and certain 2023 Carnival vehicles because the power sliding doors' auto-reverse feature may not activate in all situations, risking occupant injury.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V761000·2022-10-11

    Alamo Recalls 2021-2022 Schwarze A9SE Monsoon Street Sweepers

    Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.

    Product
    SCHWARZE — SCHWARZE A9SE MONSOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22771·2022-09-08

    Murphy Beds Recalled Due to Serious Impact and Crush Hazards

    Murphy beds sold under Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan brand names can break or detach from walls and fall, posing crush and impact hazards. The manufacturer has received 146 reports of failures with 62 injuries.

    Product
    Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan branded Murphy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1249-2022·2022-06-15

    Getinge CM320 WUWD Washer Disinfector Installation Verification Issue Recall

    The FDA is recalling 11 Getinge CM320 WUWD washer-disinfectors used for surgical instrument processing. Installation verification was not properly documented or completed, potentially creating risks of electrical shock, burns, and other injuries.

    Product
    Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber washer-disinfector for the washing, disinfecting and drying surgical instruments, Model: CM320 WUWD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·22739·2022-04-07

    Bestar Wall Beds Recalled Due to Detachment and Crush Hazards

    Bestar wall beds can detach from the wall and fall, creating impact and crush hazards. One death and 60 additional injuries have been reported.

    Product
    Bestar Wall Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22047·2022-01-11

    Residential Elevators Recalled for Child Entrapment Hazard

    Savaria and Garaventa residential elevators pose an entrapment risk to young children due to gaps between doors. Young children can become trapped and suffer serious injury or death when the elevator is called to another floor.

    Product
    Savaria and Garaventa branded residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22045·2022-01-11

    Bella Residential Elevators Recalled for Child Entrapment Hazard

    Bella residential elevators pose a risk of child entrapment between exterior and interior doors. Young children can become trapped and suffer serious injuries or death when the elevator moves to another floor.

    Product
    Bella residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E094000·2020-12-28

    Summit Racing 6-Ton Jack Stands Recalled Due to Ratchet Bar Failure Risk

    Autosales Inc. is recalling Summit Racing 6-Ton Jack Stands because the ratchet bar may fail, allowing the vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.

    Product
    EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E053000·2020-07-31

    Walmart Recalls Hyper Tough 2 Ton Jack Stands Due to Collapse Risk

    Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E046000·2020-07-07

    Harbor Freight Recalls Pittsburg Automotive 3 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling 118,000 Pittsburg Automotive 3 Ton Heavy Duty Steel Jack Stands because the base seam weld may fail under load, causing the stand to drop suddenly.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E016000·2020-03-20

    Harbor Freight Recalls Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling 454,000 Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands because the ratchet teeth may not engage properly, risking sudden failure and injury.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V528000·2019-07-12

    KME Fire Trucks Recalled for Cab Hydraulic Velocity Fuse Defect

    KME is recalling various 2016-2020 Predator and Predator Panther fire trucks because hydraulic velocity fuses may fail to lock the cab during a system failure, posing an injury risk to occupants.

    Product
    KME — KME PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER, PREDATOR SS RESCUE, PREDATOR AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2839-2018·2018-08-29

    Hitachi Scenaria CT System Recalled for Table Motion Hazard

    Hitachi is recalling one Scenaria CT system in Texas because the patient table failed to stop and contacted the gantry, posing a risk of injury.

    Product
    Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomography applications in patients of all ages. The images can be acquired in either axial, helical, gated or dynamic modes. The volume dat
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0513-2018·2018-02-14

    Philips Precedence 6 Imaging System Recalled for Collimator Drop Risk

    Philips is recalling 1,387 Precedence 6 imaging systems because collimators may drop to the floor during exchange, posing a risk of injury.

    Product
    Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acquisition of single photon nuclear medicine images and images from an x-ray computed tomography system. Precedence may produce non-attenuation corrected and attenua
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0385-2018·2018-01-24

    Fujifilm Aspire HD Plus Mammography Machines Recalled for Swivel Arm Defect

    Fujifilm is recalling Aspire HD Plus and HD-s mammography machines because the swivel arm may drop unintentionally.

    Product
    Aspire HD Plus (FDR MS-2500), also known as Aspire HD Plus F and Aspire HD-s (FDR MS-2000), also known as Aspire HD Plus S). Mammography machine The Fujifilm Digital Mammography Systems, Aspire HD Plus (FDR MS-2500) and Aspire HD-s (FDR MS-2000), generate full-field digita
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17E057000·2017-10-03

    NAPA and Evercraft 800lb Transmission Jacks Recalled for Bolt Failure

    International Specialty Services is recalling NAPA and Evercraft 800lb transmission jacks because a bolt may loosen, causing the saddle to destabilize and the transmission to tip over.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17706·2016-10-26

    Hearth & Home Technologies Recalls Quadra Fire Explorer III Wood Stoves

    Hearth & Home Technologies is recalling about 650 Quadra Fire Explorer III wood stoves because the top lid handle can disengage, causing the lid to slam shut on fingers.

    Product
    Quadra Fire® Explorer III wood stoves
    Category
    Consumer Product
    Distribution
    Distributed nationwide