BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA STRETCHER OBS 3/07

    MDR report key: 2925660 · Received January 22, 2013

    Report

    Report Number
    0001831750-2013-00282
    Event Type
    Malfunction
    Date Received
    January 22, 2013
    Date of Event
    January 3, 2013
    Report Date
    January 3, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    BRAKE CAM ASSEMBLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES WOULD NOT ENGAGE AND THE SIDERAIL WOULD NOT LATCH IN THE UPRIGHT POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30377 TRAUMA STRETCHER OBS 3/07 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1020

    Patients

    Seq Age Sex Outcome Treatment
    1