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.

126–150 of 207

  • HighFDA (Devices)·Z-0764-2016·2016-02-17

    Philips Allura Xper FD20 Ceiling Version Recalled for C-Arc Movement

    Philips is recalling 15 Allura Xper FD20 Ceiling version units because improper adjustment may cause the C-arc to continue moving after stopping.

    Product
    Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·15V726000·2015-11-03

    Forest River Recalls 2016 Recreational Vehicles Due to Shift Cable Defect

    Forest River is recalling 217 model year 2016 recreational vehicles because an incorrect shift cable bracket allows the vehicle to be shifted out of park without applying the brakes.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN FR3, GEORGETOWN, MIRADA, PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V719000·2015-10-30

    Thor Motor Coach Recalls 2016 RVs for Transmission Shift Cable Defect

    Thor Motor Coach is recalling 2016 Ace, Challenger, Hurricane, Miramar, Outlaw, and Windsport vehicles because they may shift out of park without brakes applied.

    Product
    THOR MOTOR — THOR MOTOR, THOR MOTOR COACH HURRICANE, OUTLAW, MIRAMAR, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V713000·2015-10-28

    Newmar Recalls 2016 Bay Star and Canyon Star RVs for Shift Cable Defect

    Newmar is recalling 93 model year 2016 Bay Star, Bay Star Sport, and Canyon Star vehicles because the transmission shift cable may allow shifting out of park without applying brakes.

    Product
    NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT, CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V664000·2015-10-16

    Winnebago and Itasca Motorhomes Recalled for Transmission Shift Cable Defect

    Winnebago is recalling 2015-2016 Brave, Sightseer, Vista, Adventurer, and Itasca models because they can shift out of park without brakes applied.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA SIGHTSEER, VISTA, BRAVE, ADVENTURER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V617000·2015-10-01

    Daimler Trucks Recalls 2015-2016 Freightliner and Western Star Trucks

    Daimler Trucks is recalling 2015-2016 Freightliner and Western Star trucks because the transmission may lock or cause the vehicle to move backward unexpectedly.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, BUSINESS CLASS M2, 108SD, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V611000·2015-09-30

    Ford Recalls 2016 F-53 and F-59 Trucks for Shift Cable Defect

    Ford is recalling 2016 F-53 and F-59 stripped chassis trucks because an incorrect shift cable bracket may allow the vehicle to shift out of park without brakes applied.

    Product
    FORD — FORD F-53, F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V463000·2015-07-24

    General Motors Recalls 2013-2016 Cadillac ATS for Sunroof Defect

    General Motors is recalling 2013-2016 Cadillac ATS vehicles because the sunroof may close automatically if the switch is pressed inadvertently, posing a risk of personal injury.

    Product
    CADILLAC — CADILLAC ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15195·2015-07-23

    Husqvarna Recalls Lawn Tillers Due to Unintended Movement Risk

    Husqvarna is recalling approximately 24,000 Ariens, Husqvarna, Jonsered, and Poulan Pro tillers because the transmission shift rod can cause the machine to move unintentionally, posing a risk of injury.

    Product
    Lawn and garden tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V436000·2015-07-08

    Ford Recalls 2015 Focus, C-Max, and Escape for Engine Shutdown Defect

    Ford is recalling 2015 Focus, C-Max, and Escape vehicles because the engine may continue running after being turned off, increasing the risk of an unintentional crash.

    Product
    FORD — FORD FOCUS, C-MAX, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1795-2015·2015-06-24

    Neuro Kinetics Recalls I-Portal NOTC and VNG Devices Due to Malfunction

    Neuro Kinetics is recalling 140 I-Portal NOTC and VNG devices due to system malfunctions and unintended sudden movements at startup. No injuries have been reported.

    Product
    I-Portal¿ NOTC and VNG; a device used to measure, record, or visually display the involuntary movements (nystagmus) of the eyeball, indicated for use as a diagnostic tool to assist trained clinicians in their analysis of vestibular disorders, which requires the separation of cent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1745-2015·2015-06-17

    AGFA DX-D 100 Mobile X-Ray System Recalled for Unintended Movement

    AGFA Healthcare Corp. is recalling 233 mobile digital radiography x-ray systems due to a risk of sporadic unintended movements caused by electrostatic discharge.

    Product
    AGFA DX-D 100 is a mobile digital radiography x-ray system
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-1449-2015·2015-04-22

    Hansen Medical Recalls Magellan Robotic Systems Due to Catheter Retraction Defect

    Hansen Medical is recalling 19 Magellan Robotic Systems because the catheter may fail to stop retracting when the control button is released.

    Product
    Magellan Robotic System; Model No(s). 11132 and 11139. A steerable catheter control system used at clinical sites.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1394-2015·2015-04-15

    Toshiba INFX-8000V Interventional Angiography System Recall for Brake Defect

    Toshiba is recalling 28 INFX-8000V Interventional Angiography Systems because the table base rotational brake may not engage when force is applied to the table top.

    Product
    INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V se
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1011-2015·2015-02-04

    Philips BrightView MRI Systems Recalled for Unintended Movement

    Philips is recalling 1,064 BrightView MRI systems worldwide due to software issues causing unintended detector and gantry movement.

    Product
    BrightView model number: 882478 BrightView X model number: 882480 BrightView XCT model number: 882482 and 882454 Medical Device for imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0996-2015·2015-01-28

    TransMotion Medical Recalls Powered Stretcher Chairs Due to Involuntary Movement

    TransMotion Medical Inc is recalling 1,127 powered stretcher chairs used in surgeries because the controllers may cause the chairs to move involuntarily.

    Product
    Powered stretcher chair used during facial and eye surgeries. One chair per package.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0993-2015·2015-01-28

    Maquet Tegris System Recalled Due to Software Error in Operating Table Commands

    Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.

    Product
    TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0921-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER U Remote Controls for Unintended Movement

    Trumpf Medical Systems is recalling JUPITER U remote controls because damaged units may cause unintended movement of operating tables during surgery.

    Product
    IR remote control JUPITER U, Material no. 4500120, Serial number: to (incl.) 102306940. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer sys
    Category
    Medical Device
    Distribution
    25 states
  • SevereFDA (Devices)·Z-0924-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Remote Controls Due to Unintended Movement

    Trumpf Medical Systems is recalling JUPITER remote controls used with operating tables because complaints were reported of unintended movement during surgical cases.

    Product
    (R)IR remote control JUPITER, Material no.1219656, Serial number: to (incl.) 102317869. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer sys
    Category
    Medical Device
    Distribution
    25 states
  • SevereFDA (Devices)·Z-0923-2015·2015-01-14

    Trumpf Medical Systems Recalls IIR Remote Controls for Operating Tables

    Trumpf Medical Systems is recalling IIR remote controls for JUPITER operating tables due to reports of unintended movement during surgery.

    Product
    IIR remote control JUPITER, Material no.4544120, Serial number: to (incl.) 102006720. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer syste
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0919-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls because damaged units may cause unintended movement during surgery.

    Product
    Cable remote control JUPITER / TS7500, Material no.1601926, Serial number: to (incl.) 101465919. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient tra
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0920-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Cable Remote Controls

    Trumpf Medical Systems is recalling JUPITER cable remote controls due to reports of unintended movement during surgical cases.

    Product
    Cable remote control JUPITER, Material no. 4544119, Serial number: to (incl.) 102284378. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer sy
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0922-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Remote Controls Due to Unintended Movement

    Trumpf Medical Systems is recalling JUPITER remote controls for operating tables because damaged units may cause unintended movement during surgery.

    Product
    IR remote control JUPITER / TS7500, Material no.1601927, Serial number: to (incl.) 102222333. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transf
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0925-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Remote Controls for Unintended Movement

    Trumpf Medical Systems is recalling JUPITER remote controls used with operating tables due to reports of unintended movement during surgical cases.

    Product
    (R)Cable remote control JUPITER, Material no.1219655, Serial number: to (incl.) 101998119. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0927-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls because damaged units may cause unintended movement during surgery.

    Product
    IR remote control JUX, Material no.1307314, Serial number: to (incl.) 102338310 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to t
    Category
    Medical Device
    Distribution
    25 states