BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA STRETCHER OBS 3/07

    MDR report key: 2911287 · Received January 11, 2013

    Report

    Report Number
    0001831750-2013-00030
    Event Type
    Malfunction
    Date Received
    January 11, 2013
    Date of Event
    December 20, 2012
    Report Date
    December 20, 2012
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LEFT SIDE RAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    19107 TRAUMA STRETCHER OBS 3/07 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1020

    Patients

    Seq Age Sex Outcome Treatment
    1