The Recall Desk

Hazard

Collision recalls

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

What the numbers show

Total
56
Critical
0
Severe
15
Most recent
2026-08-12

Of the 56 collision recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 15 (27%) 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 collision 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 56

  • SevereFDA (Devices)·Z-2856-2026·2026-08-12

    Powered Wheelchair Control Software Recall by munevo

    Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.

    Product
    munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·26632·2026-07-30

    TT Trsmima zipline kits and spring brakes recalled for fall and collision hazards

    TT Trsmima backyard zipline kits and spring brakes can break, detach or fail to slow riders. Reports include fractures, concussions, sprains and abrasions across two separate failure modes.

    Product
    TT Trsmima Zipline Kits and Zipline Spring Brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25E034000·2025-05-12

    Waymo Recalls 5th Generation Automated Driving Systems for Collision Risk

    Waymo is recalling 5th Generation Automated Driving Systems with older software that may cause vehicles to collide with roadway barriers like chains and gates.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2025·2025-04-30

    Philips Brilliance CT Big Bore X-Ray System Gantry Motion Collision Hazard

    Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.

    Product
    Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24326·2024-08-01

    Peace Sports Youth ATVs Recalled for Safety Violations and Injury Risk

    Peace Industry Group is recalling about 1,000 Peace Sports Youth All-Terrain Vehicles due to violations of federal ATV safety standards. The ATVs have defective handlebars, faulty parking brakes, missing reflectors, and footguards that pose risks of laceration, amputation, and collision.

    Product
    Peace Sports Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23191·2023-04-27

    EGL Motor ACE Youth ATVs Fail Safety Standards; Risk of Injury or Death

    EGL Motor is recalling about 4,000 ACE-branded youth all-terrain vehicles (ATVs) that fail federal safety standards. The K125 and C125 models exceed maximum speed limits, and the T125 and C125 models have faulty parking brakes, posing risks of high-speed crashes and collisions.

    Product
    EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1168-2023·2023-03-01

    Diagnostic imaging system recalled due to ceiling and wall collision risk

    Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.

    Product
    Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1160-2021·2021-03-10

    United Imaging X-ray System Recalled for Uncommanded Motion Hazard

    Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.

    Product
    Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0556-2021·2020-12-16

    Shimadzu MH-200S X-Ray System Recalled for Ceiling Arm Software Defect

    Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.

    Product
    MH-200S, system with Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0554-2021·2020-12-16

    Shimadzu Bransist Safire Digital Angiography System Recalled for Software Defect

    Shimadzu Medical Systems is recalling seven Bransist Safire Digital Angiography Systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm.

    Product
    Bransist Safire, Digital Angiography System containing a MS-200 Ceiling Suspended C-arm Support - Product Usage: designed to provide fluoroscopic images of the patient during diagnostic surgical and interventional angiography and cardiology procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0555-2021·2020-12-16

    Shimadzu Trinias Digital Angiography System Recalled for Ceiling Arm Software Issue

    Shimadzu is recalling 23 Trinias Digital Angiography Systems because a software defect may cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.

    Product
    Trinias, Digital Angiography System containing a MH-200, Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0108-2021·2020-10-21

    Siemens Artis zee and Q Systems Recalled for Collision Risk

    Siemens Medical Solutions is recalling Artis zee and Artis Q systems because a software defect may cause the equipment to collide with room fixtures or patients.

    Product
    Artis zee or Artis Q systems (listed below) - Product Usage: for single and biplane diagnostic imaging and interventional procedures. System Name/Material Number: Artis Q BIPLANE 10848282 ARTIS Q CEILING 10848281 Artis Q floor 10848280 ARTIS Q ZEEGO 10848283 ARTIS Q.ZEN B
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2758-2020·2020-08-12

    Siemens Ysio Max X-Ray System Recalled for Software Defects

    Siemens Medical Solutions is recalling 512 Ysio Max X-ray systems due to software issues that may cause collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System, Model: 10762470 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2755-2020·2020-08-12

    Siemens Luminos dRF Max Recalled for Software Collision and Image Errors

    Siemens is recalling 49 Luminos dRF Max units due to software defects that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2757-2020·2020-08-12

    Siemens Uroskop Omnia Max Recalled for Software Collision and Image Errors

    Siemens is recalling 194 Uroskop Omnia Max units due to software issues that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2756-2020·2020-08-12

    Siemens Luminos Agile Max Recalled for Software Collision and Image Errors

    Siemens Medical Solutions is recalling 477 Luminos Agile Max units due to software defects that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1333-2020·2020-02-26

    Siemens Uroskop Omnia max Recalled for Collision Control Override Risk

    Siemens is recalling 192 Uroskop Omnia max devices because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.

    Product
    Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological therapeutic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2020·2020-02-26

    Siemens Luminos dRF Max Recalled for Collision Control Override Risk

    Siemens is recalling 46 Luminos dRF Max devices because an override function can disable collision controls, creating a risk of collision with obstacles or persons.

    Product
    Luminos dRF Max, Model No. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal, t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20713·2020-01-30

    Polaris Recalls 2017-2018 Brutus UTVs Due to Rear Brake Line Failure

    Polaris is recalling 2017-2018 Brutus utility vehicles because a rear brake line can puncture, causing brake failure and a crash hazard.

    Product
    Model Year 2017-2018 Brutus Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20714·2020-01-30

    Polaris Recalls 2019 Pro XD Utility Vehicles Due to Rear Brake Failure Risk

    Polaris is recalling about 760 Model Year 2019 Pro XD utility vehicles because the rear brake line can puncture, causing rear brake failure and posing a crash hazard.

    Product
    Model Year 2019 Polaris PRO XD Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18150·2018-05-08

    Hauck Recalls Nerf Battle Racer Go-Karts Due to Steering Wheel Hazards

    Hauck is recalling Nerf Battle Racer go-karts because the steering wheel can detach, break, or crack, posing laceration and collision risks to children.

    Product
    Hauck Nerf® Battle Racer go-karts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1400-2018·2018-04-25

    Siemens ONCOR Impression Linear Accelerator Software Update Recall

    Siemens is recalling seven ONCOR Impression Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Impression , Digital Linear Accelerator, Model No. 05857920 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1399-2018·2018-04-25

    Siemens Oncor Expression Linear Accelerator Software Update Recall

    Siemens is recalling two Oncor Expression linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Expression, Digital Linear Accelerator, Model No. 07360717 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide