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.

1–25 of 87

  • HighNHTSA·26V394000·2026-06-18

    2026–2027 Cadillac Vistiq Third-Row Seat Power Fold Feature Recall

    General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V160000·2026-03-17

    2026 Hyundai Palisade power rear seats may fail to detect occupants

    Hyundai is recalling 2026 Palisade and Palisade Hybrid vehicles with Limited or Calligraphy trim because the second and third row power seats may fail to detect a person and continue moving, risking entrapment or injury.

    Product
    HYUNDAI — HYUNDAI PALISADE, PALISADE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V020000·2026-01-19

    Fifth wheel trailer ramp door may break away from its frame

    Forest River is recalling certain fifth wheel travel trailers across the Work and Play, Coachmen Adrenaline, Chaparral, Riverstone, Takoda, Shasta Phoenix and Cedar Creek ranges because the ramp door may break away.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, SHASTA CEDAR CREEK, CHAPARRAL, RIVERSTONE, ADRENALINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V283000·2025-05-01

    2025 Keystone Kodiak Travel Trailers Recalled for Defective Patio Support Struts

    Keystone is recalling certain 2025 Kodiak travel trailers because the patio support struts may not adequately support the fold-down patio's weight, increasing the risk of injury. Owners should contact Keystone or their dealer for free repair.

    Product
    KEYSTONE — KEYSTONE KODIAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25136·2025-02-13

    Igloo Rolling Coolers Recalled for Fingertip Amputation and Crushing Hazards

    Igloo is recalling approximately 1.06 million 90-quart rolling coolers because the tow handle can pinch fingertips against the cooler. The company has received 12 reports of fingertip injuries, including amputations and bone fractures.

    Product
    Igloo 90 Qt. Flip & Tow Rolling Coolers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1080-2025·2025-02-12

    Philips recalls AlluraXper FD20 patient tables due to finger entrapment hazard

    Philips is recalling AlluraXper FD20 patient tables due to a finger entrapment hazard. During manual repositioning, fingers can get trapped between the tabletop and rails, risking injury to operators and service personnel.

    Product
    AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1092-2025·2025-02-12

    Philips Azurion patient tables recalled for finger entrapment hazard

    Philips is recalling Azurion 7 B20 patient tables due to a finger entrapment hazard between the tabletop and guiding rails during manual repositioning. Operators and service personnel could suffer finger injury.

    Product
    Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1085-2025·2025-02-12

    Finger entrapment hazard in Philips Allura fluoroscopy patient tables

    Philips is recalling AD7 and AD7X patient tables from Allura and Azurion fluoroscopy systems. During manual repositioning, fingers can become trapped between the guiding rails and tabletop, potentially causing injury.

    Product
    Allura Xper FD20/20 System Code: (1) 722038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2025·2025-02-12

    Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk

    Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.

    Product
    AlluraXperFD20/10 System Code: (1) 722029
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2025·2025-02-12

    Philips Allura CV20 patient tables risk finger entrapment during repositioning

    The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.

    Product
    Allura CV20 System Code: 722031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1082-2025·2025-02-12

    Philips AlluraXper FD20 operating room surgical table finger entrapment risk

    Philips AlluraXper FD20 operating room tables can trap fingers during manual repositioning, risking injury. The hazard affects both operators and service personnel worldwide.

    Product
    AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2025·2025-02-12

    Philips AlluraXper Operating Room Table Finger Entrapment Hazard

    The Philips AlluraXper FD20 operating room table can trap fingers between the guiding rails and tabletop during manual repositioning, potentially injuring operators and service personnel.

    Product
    AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1081-2025·2025-02-12

    Philips AlluraXper FD20 Biplane Patient Table Finger Entrapment Risk

    Philips AlluraXper FD20 Biplane patient tables may cause finger entrapment between the tabletop and guiding rails during manual repositioning, affecting operators and service personnel.

    Product
    AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1087-2025·2025-02-12

    Philips Azurion and Allura Patient Tables: Finger Entrapment Hazard

    Philips patient tables on Azurion and Allura imaging systems can trap fingers between the tabletop and rails during manual repositioning. Operators and service personnel are at risk of finger injury.

    Product
    Azurion 3 M12 System Code: (1) 722063 (2) 722221
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2025·2025-02-12

    Philips Azurion Patient Tables Recalled for Finger Entrapment Risk

    Philips Azurion patient tables used in medical imaging systems can trap fingers between the tabletop and rails during manual repositioning, potentially causing finger injury to operators and service personnel.

    Product
    Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25080·2024-12-26

    Inclusive Orbit merry-go-rounds recalled due to finger crush hazard

    About 415 Inclusive Orbit merry-go-rounds are recalled due to a crushing hazard where the gap between the rotating platform and outer rim narrows, trapping children's fingers. Two finger crushing injuries have been reported.

    Product
    Inclusive Orbit merry-go-rounds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25053·2024-11-21

    Dorel Wall Beds Recalled for Serious Detachment and Crush Hazards

    About 69,300 Dorel wall beds sold online may detach from the wall and fall. The manufacturer has received 22 reports of beds falling, resulting in 10 injuries including concussions and contusions.

    Product
    Dorel Wall Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2527-2024·2024-08-14

    Medical X-ray display system support arm may lower unexpectedly

    Siemens LUMINOS Lotus Max X-ray displays are being recalled because the support arm may lower unintentionally, potentially injuring people nearby during positioning.

    Product
    LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24208·2024-04-25

    Oregon Tool Recalls Log Splitters Due to Injury Hazards

    Oregon Tool is recalling about 29,560 log splitters and cylinder kits because the hydraulic cylinder rod can separate from the piston, causing unexpected movement of the wedge that poses injury risks. No injuries have been reported.

    Product
    Oregon, PowerPro, Country Tuff, and Speeco branded log splitters and cylinder kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0679-2024·2024-01-17

    Gamma Camera Recalls Due to Potential Patient Extremity Entrapment Hazard

    Philips BrightView XCT gamma cameras may pose an extremity entrapment hazard during certain scanning operations. A gap can form between the patient support and detector, risking fractures, lacerations, and crush injuries.

    Product
    BrightView XCT, Gamma Camera, Product Code 882482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2024·2024-01-17

    Philips BrightView Gamma Camera System Recalled for Extremity Entrapment Hazard

    Philips is recalling BrightView Gamma Camera Systems because a gap can form between patient support and detector during quality assurance scans, creating an extremity entrapment hazard that may cause fractures or crush injuries.

    Product
    BrightView, Gamma Camera System, Product Code 882480.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0678-2024·2024-01-17

    Gamma Camera Gap Creates Extremity Entrapment Hazard During Quality Assurance

    Philips BrightView X gamma cameras may create a gap between patient support and detector during quality assurance scans, potentially trapping a patient's extremity.

    Product
    BrightView X, Gamma Camera, Product Code 882478
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·24082·2024-01-11

    Justin Boots Keaven WP Met Guard Work Boots Recalled Due to Missing Metatarsal Guard

    Boot Royalty is recalling about 3,200 Justin Boots Keaven WP Met Guard Work Boots (Model SE4570) because the metatarsal guard may be missing, creating a crush hazard to the wearer's feet. One injury has been reported.

    Product
    Justin Boots Keaven WP Met Guard Work Boots Model SE4570
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23287·2023-09-14

    Honda Lawnmowers and Pressure Washer Engines Recall Due to Starter Rope Injury Hazard

    American Honda is recalling about 391,800 lawnmowers and pressure washer engines because improperly manufactured camshafts can cause the starter rope to suddenly retract when pulled, posing an injury hazard. The company has received 2,197 reports of incidents, including seven minor injuries.

    Product
    Honda Lawnmowers and Pressure Washer Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide