The Recall Desk

Hazard

Unintended Movement recalls

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

What the numbers show

Total
207
Critical
7
Severe
75
Most recent
2026-07-22

Of the 207 unintended movement recalls we have scored against our rubric, 7 (3%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 75 (36%) 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 unintended 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.

101–125 of 207

  • HighFDA (Devices)·Z-1266-2018·2018-04-04

    Deerfield Imaging Recalls IMRIS ORT300 Operating Room Tables Due to Drift Risk

    Deerfield Imaging is recalling 13 IMRIS ORT300 operating room tables because they may drift during use, potentially causing unintended movement.

    Product
    IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1265-2018·2018-04-04

    Deerfield Imaging Recalls IMRIS T2X Operating Room Tables

    Deerfield Imaging is recalling 14 IMRIS T2X Operating Room Tables because they may drift during use, potentially causing unintended movement.

    Product
    IMRIS T2X Table, Part Numbers: (a) 108000-000 (b) 108000-600 (c) 109682-000 (d) 109682-600
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1263-2018·2018-04-04

    Deerfield Imaging Recalls IMRIS ORT100 Operating Room Tables

    Deerfield Imaging is recalling 26 IMRIS ORT100 operating room tables because they may drift during use, potentially causing unintended movement.

    Product
    IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1264-2018·2018-04-04

    Deerfield Imaging Recalls IMRIS ORT200 Operating Room Tables for Drift Risk

    Deerfield Imaging is recalling 17 IMRIS ORT200 operating room tables because they may drift during use, potentially causing unintended movement.

    Product
    IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0976-2018·2018-03-21

    Deerfield IMRIS T2X Table Recall Due to Rotational Locking Defect

    Deerfield Imaging is recalling 16 IMRIS T2X tables because the rotational locking mechanisms can disengage, potentially causing unintended table movement.

    Product
    IMRIS T2X Table, Part Number 109682-600
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·18V109000·2018-02-14

    Lance Recalls 2018 Recreational Trailers Due to Power Tongue Jack Defect

    Lance is recalling 2018 recreational trailers because a power tongue jack touch pad may crack, allowing water entry and causing the jack to operate unintentionally.

    Product
    LANCE — LANCE 1995, 2465, 2185, 2285
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V059000·2018-01-16

    Liberty Recalls 2018 Little Guy Max Trailers Due to Jack Defect

    Liberty is recalling 2018 Little Guy Max trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.

    Product
    LIBERTY — LIBERTY LITTLE GUY MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V008000·2018-01-08

    Terex Recalls 2015-2017 XT Pro Aerial Devices for Control Defect

    Terex is recalling 2015-2017 XT Pro 56 and 60 aerial devices because the platform control enable system may be adjusted incorrectly, increasing injury risk.

    Product
    TEREX — TEREX XT PRO 60, XT PRO 56
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V840000·2017-12-22

    PACCAR Recalls 2018 Kenworth and Peterbilt Trucks for Transmission Defect

    PACCAR is recalling 2018 Kenworth and Peterbilt trucks because the transmission control module may allow the engine to start without the shifter in neutral, risking unintended movement.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, T880, 567, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E078000·2017-12-20

    Eaton Cummins Transmission Recall for Unintended Vehicle Movement Risk

    Eaton Cummins is recalling specific Endurant and PACCAR transmissions where the control module may allow the engine to crank if the shifter is not in neutral, increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E074000·2017-12-15

    Lippert Smart Jack Power Tongue Jack Recall for Unintended Movement

    Lippert is recalling Smart Jack model 426514 Power Tongue Jacks because the touch pad can crack, allowing water entry that causes the jack to move unexpectedly.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0160-2018·2017-11-29

    FDA Recalls Zimmer Biomet ROSA Surgical Devices Due to Sensor Failure

    The FDA is recalling 31 Zimmer Biomet ROSA Surgical Devices because a force feedback sensor may fail, causing the operating arm to continue moving instead of stopping.

    Product
    ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0115-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Surgical Device Due to Software Error

    Zimmer Biomet is recalling 64 ROSA Surgical Device 2.5.8 units because a software defect may change tool orientation without user command.

    Product
    ROSA Surgical Device 2.5.8
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0105-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Brain 3.0 Neurosurgical Devices

    Zimmer Biomet is recalling three ROSA Brain 3.0 neurosurgical devices due to insufficient washers in the telescopic arm that allow unwanted movement.

    Product
    ROSA Brain 3.0 Intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments. The device is indicated for any neurosurgical procedure in which the use of stereotactic surgery may
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-3222-2017·2017-10-04

    Teleflex Percuvance Maryland Dissector Tool Tip Recall for Connection Issues

    Teleflex Medical is recalling Percuvance Maryland Dissector Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.

    Product
    Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-3223-2017·2017-10-04

    Teleflex Percuvance Scissors Tool Tip Recall for Connection and Jaw Issues

    Teleflex Medical is recalling Percuvance Scissors Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.

    Product
    Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft ti
    Category
    Medical Device
    Distribution
    29 states
  • HighNHTSA·16V805000·2016-11-04

    Terex Recalls 2009-2014 TC and TCX Trucks for Wiring Defect

    Terex is recalling 2009-2014 TC and TCX hybrid electric trucks because improper wiring may cause the aerial boom to move unintentionally, increasing the risk of injury.

    Product
    TEREX — TEREX TC, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V712000·2016-10-05

    Daimler Recalls 2017 Thomas Built Buses Saf-T-Liner C2 School Bus Chassis

    Daimler Trucks North America is recalling 162 model year 2017 Thomas Built Buses Saf-T-Liner C2 school bus chassis because the brake transmission shift interlock may be inoperable.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V504000·2016-07-05

    Jerr-Dan Recalls 2014-2016 HDR 1000 Wrecker Trucks Due to Control Defect

    Jerr-Dan is recalling 24 model year 2014-2016 HDR 1000 wrecker trucks because vehicle-mounted controls may remain engaged, causing unintended equipment movement and injury risk.

    Product
    JERR-DAN — JERR-DAN HDR 1000
    Category
    Vehicle
    Distribution
    Distributed nationwide