The Recall Desk

Hazard

Pinch Injury recalls

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

What the numbers show

Total
53
Critical
0
Severe
4
Most recent
2026-06-09

Of the 53 pinch injury 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 (8%) 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 pinch 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.

26–50 of 53

  • HighFDA (Devices)·Z-0914-2015·2015-01-14

    Siemens e.cam Systems Recalled for Potential Patient Finger Injury

    Siemens Medical Solutions is recalling 4,462 e.cam emission computed tomography systems due to a potential risk of patient finger injury.

    Product
    e.cam -emission computed tomography system Used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2014·2014-07-09

    Siemens MicroScan WalkAway Plus Instruments Recalled for Hinge Spring Failure

    Siemens is recalling MicroScan WalkAway-40 and 96 plus instruments because springs in the access door hinge assembly are detaching, causing premature failure and potential safety issues.

    Product
    MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus instrument access door hinge. Siemens Healthcare Diagnostics, Inc. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0787-2014·2014-01-29

    Siemens Linac Treatment Table Recall for Finger Pinch and Cable Damage

    Siemens is recalling 305 linear accelerator treatment tables due to risks of finger pinching and cable short-circuits.

    Product
    PRIMUS, ONCOR, ARTISTE Linac systems with component 550 TxT Treatment Table. TT-A, TT-D, TT-M or TT-S Table tops. Manufactured by: SIEMENS AG, MEDICAL SOLUTIONS Roentgenstrasse 19-21 Kemnath, GERMANY 95478 The intended use of the SIEMENS branded, ARTISTE", ONCOR" a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V504000·2013-10-17

    Blue Bird School Bus Recall for Flip Seat Pinch Hazard

    A-Z Bus Sales is recalling 2005-2013 Blue Bird A3RE and D3RE school buses to fix a pinch point hazard in C.E. White flip seats.

    Product
    BLUE BIRD — BLUE BIRD D3RE, A3RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V371000·2013-08-16

    TCI School Bus Flip Seat Pinch Hazard Recall

    TCI is recalling specific school buses with C.E. White flip seats due to a risk of foot or toe pinch injuries for rearward passengers.

    Product
    TCI — TCI DW6159RLSST, SC159DSFP600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V320000·2013-07-23

    Navistar Recalls IC School Buses for Flip Seat Pinch Hazard

    Navistar is recalling certain IC school buses equipped with C. E. White Inc. flip seats due to a risk of foot or toe pinch injuries.

    Product
    IC BUS — IC BUS, IC RESB, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1622-2013·2013-07-10

    Maquet YUNO Mobile Operating Table Recall for Extension Device Handle Issue

    Maquet is recalling YUNO mobile operating tables and extension devices because the handle design may allow operator skin to enter a gap.

    Product
    MAQUET Getinge Group Mobile Operating Table YUNO OTN GA 1433.01 EN 05. The YUNO OTN is used to support and position patients for surgical procedures immediately before, during and after the surgical phase. The table top is radio translucent and enables intraoperative use of X-
    Category
    Medical Device
    Distribution
    6 states
  • HighNHTSA·13V200000·2013-05-15

    Blue Bird Recalls School Buses with Flip Seat Pinch Hazard

    Blue Bird is recalling 2010-2014 All American and Vision school buses equipped with specific C. E. White Flip Seats due to a risk of foot or toe pinch injuries.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1168-2013·2013-05-01

    GE Healthcare Recalls Ventri Discovery NM 530c Nuclear Imaging Systems

    GE Healthcare is recalling 556 Ventri Discovery NM 530c nuclear imaging systems because a moving table mechanism can pinch patient fingers during an exam.

    Product
    Ventri Discovery NM 530c, Ventri with Premium Table Discovery NM 530c, models H3000ZW & H3000SA. The system is used to perform nuclear imaging procedures.
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-1166-2013·2013-05-01

    Philips NeuViz Dual CT Scanner Recalled for Pinch Hazard

    Philips and Neusoft are recalling 25 NeuViz Dual CT scanners because user error can cause personnel injuries, including a reported finger pinch.

    Product
    NeuViz Dual series CT Scanner System, Part number (PN): 989605651321. This is a computed X-ray, Tomography system. NeuViz Dual Multi-slice CT Scanner System is intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data ta
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1165-2013·2013-05-01

    Philips NeuViz 16 CT Scanner Recalled Due to Pinch Hazard

    Philips and Neusoft are recalling 23 NeuViz 16 CT scanners because a user error could cause personnel injuries, including a reported finger pinch.

    Product
    NeuViz 16 Multi-Slice CT Scanner System, Part number (PN): 989605858501, Model: NeuViz 16. This is a computed X-ray, Tomography system. The NeuViz 16 CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13E020000·2013-04-23

    C. E. White Recalls School Bus Flip Seats for Pinch Hazard

    C. E. White is recalling specific school bus flip seats installed between 2005 and 2013 because the lower frame gap can pinch the toes or feet of passengers in rearward seats.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1790-2012·2012-06-20

    GE Proteus XR/a Radiographic System Recalled Due to Pinch Hazard

    General Electric is recalling 3,796 Proteus XR/a Radiographic Systems worldwide because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic a
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1788-2012·2012-06-20

    GE Healthcare Revolution XR/d Recalled for Finger Pinch Hazard

    General Electric is recalling 3,796 Revolution XR/d digital radiographic imaging systems worldwide due to a reported incident where an operator's finger was pinched.

    Product
    GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model numbers: 2259988-2 & 2351505. The Revolution XR/d Digital Radiographic Imaging System is indicated for use in generating radiographic images of human anatomy. It is intended to repl
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1789-2012·2012-06-20

    GE Healthcare Definium 8000 Digital Radiographic Systems Recalled for Pinch Hazard

    General Electric is recalling 3,796 Definium 8000 Digital Radiographic Systems because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model Number: 5131070. The Revolution XR/d with Tomosynthesis is intended for use in generating Tomographic images of human anatomy. It is not intended for m
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·11V538000·2011-11-04

    Nissan Recalls Infiniti G37 and 370Z for Power Window Defect

    Nissan is recalling certain 2011-2012 Infiniti G37 and 2011 Nissan 370Z vehicles because a programming error in the power window switch may increase the risk of pinch injuries.

    Product
    INFINITI — INFINITI, NISSAN G37, 370Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·10V654000·2010-12-22

    Kenworth Recalls 2011 T660 and T700 Tractors for Hood Latch Defect

    Kenworth is recalling 1,510 model year 2011 T660 and T700 tractor trailers because the hood safety latch may fail, allowing the hood to close unexpectedly.

    Product
    KENWORTH — KENWORTH T700, T660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·03121·2003-05-06

    Baby's Dream Recalls Wooden Convertible Cribs Due to Hinge and Latch Defects

    Baby's Dream Furniture is recalling approximately 4,600 wooden convertible cribs because hinges may crack or latches may fail, posing pinch and fall hazards.

    Product
    Wooden convertible cribs sold under the following model names: "Always Crib," "Crib 4 Life," "Legendary Crib," "Set 4 Life," and "Crib-2-College"
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·01210·2001-07-31

    Fisher-Price Recalls Portable Bassinets Due to Finger Pinch Hazard

    Fisher-Price is recalling about 569,000 portable bassinets because the folding mechanism can pinch or cut fingers. Consumers should stop using them and order a free repair kit.

    Product
    Portable bassinet sold under the names Sit & Soothe Portable Bassinet, Soothing Sounds Bassinet, and Soothing Sounds Portable Bassinet
    Category
    Consumer Product
    Distribution
    Distributed nationwide