BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1780121 · Received May 6, 2010

    Report

    Report Number
    1824206-2010-06981
    Event Type
    Malfunction
    Date Received
    May 6, 2010
    Date of Event
    January 26, 2007
    Report Date
    January 26, 2007
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE GAS SPRING, WHICH RESOLVED THE ISSUE. THE DEVICE FUNCTIONS AS DESIGNED. PURSUANT TO OUR RESPONSE TO WARNING LETTER 2008-DT-04, HILL-ROM IS CONTINUING ITS RETROSPECTIVE REVIEW OF EVENTS FOR REPORTABILITY. THIS EFFORT WILL CONTINUE UNTIL WE ARE CURRENT.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGES THAT THE HEAD SECTION WILL NOT LOWER, RESULTING IN NO CPR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. P8000B5SSH13PN

    Patients

    Seq Age Sex Outcome Treatment
    1