The Recall Desk

Hazard

Unintentional Movement recalls

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

What the numbers show

Total
13
Critical
0
Severe
4
Most recent
2024-01-10

Of the 13 unintentional movement recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (31%) 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 unintentional movement 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.

1–13 of 13

  • SevereNHTSA·24V013000·2024-01-10

    Western Star 4900 and 6900 Trucks Recalled for Parking Brake Defect

    Daimler Trucks North America is recalling 2023 Western Star 4900 and 6900 trucks because a parking brake defect may allow the vehicle to move unintentionally.

    Product
    WESTERN STAR — WESTERN STAR 6900, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V007000·2024-01-08

    Marion Body Works Recalls 2024 Spartan Fire MetroStar Vehicles for Brake Defect

    Marion Body Works is recalling 2024 Spartan Fire MetroStar vehicles because a defective inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V798000·2023-11-26

    KME Fire Trucks Recalled for Parking Brake Defect

    KME is recalling 2021-2023 fire trucks because a valve defect may delay parking brake engagement, increasing crash risk.

    Product
    KME — KME redundant PREDATOR, SEVERE SERVICE, PREDATOR, redundant PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V748000·2023-11-07

    Alexis Fire Equipment Recalls Fire Apparatus Due to Parking Brake Defect

    Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V747000·2023-11-07

    Spartan Fire Emergency Vehicles Recalled for Parking Brake Defect

    Custom Fire Apparatus is recalling 2021-2024 Spartan emergency vehicles because a parking brake defect may allow unintentional movement, increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, FC-94, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V631000·2023-09-12

    Spartan Fire Recalls Emergency Vehicles Due to Parking Brake Defect

    Spartan Fire is recalling 660 emergency vehicles because a parking brake defect may allow the vehicle to move unintentionally.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME GLADIATOR, FC-94, METROSTAR, redundant PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V456000·2021-06-17

    Terex Advance Recalls 2021 Front Discharge Mixers Due to Chute Defect

    Terex Advance is recalling 188 units of 2021 Front Discharge Mixers because a shaft key was not installed properly, which could cause unintentional chute movement and increase the risk of injury.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V050000·2020-01-29

    Vactor 2100i Vehicles Recalled for Safety Interlock Software Defect

    Vactor is recalling 2017-2020 2100i vehicles because a software defect may cause safety interlocks to fail, leading to unintentional vehicle movement and increased crash risk.

    Product
    VACTOR — VACTOR 2100I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0659-2019·2018-12-26

    Konica Minolta Recalls 151 X-Ray Systems Due to Unintentional Movement

    Konica Minolta is recalling 151 Advanced Universal U-Arm 4000 X-ray systems because the U-Arm may move unintentionally.

    Product
    Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17; Board Name; Board Version, Firmware Version Advanced Universal U-Arm 4000 System. The Positioner consists of the following associated subassemblies: Vertical Column, Swivel Arm with variable height, X-ray T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2739-2018·2018-08-15

    VitalGo Total Lift Bed Recalled for Unintentional Support Surface Movement

    Vitalgo Inc. is recalling 85 VitalGo Total Lift Beds in Texas due to a risk of the support surface moving unintentionally from a tilted to a horizontal position.

    Product
    VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1585-2016·2016-05-04

    Shimadzu X-Ray Diagnostic Table Recalled for Unintentional Reverse Tilting

    Shimadzu Medical Systems is recalling 185 X-Ray Diagnostic Tables (Model YSF-300) due to reports of unintentional movement to reverse tilting.

    Product
    X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier and X-ray television unit, this table is applied for the following X-ray examinations: -X-ray T.V. fluoroscopy -Spot-filming -Bucky radiogr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0651-2016·2016-02-03

    Midmark Vantage Panoramic X-Ray System Recalled for Collimator Failure

    Midmark Corp dba Progeny Inc is recalling 832 Vantage Panoramic X-Ray Systems because a primary collimator failure may cause unintentional movement without an error message.

    Product
    Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray System is a class II extra oral X-Ray system used to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw and oral structures.
    Category
    Medical Device
    Distribution
    34 states