BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER OBS 3/07

    MDR report key: 2954790 · Received February 11, 2013

    Report

    Report Number
    0001831750-2013-00957
    Event Type
    Malfunction
    Date Received
    February 11, 2013
    Date of Event
    January 18, 2013
    Report Date
    January 18, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE NECK SECTION COULD NOT LOCK IN PLACE AND HOLD WEIGHT DUE TO THE NECK CABLE RELEASE MALFUNCTIONING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    59691 EYE SURGERY STRETCHER OBS 3/07 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1069

    Patients

    Seq Age Sex Outcome Treatment
    1