BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2100090 · Received May 16, 2011

    Report

    Report Number
    1824206-2011-02717
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    April 25, 2011
    Report Date
    April 25, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND THE HEX ROD AT THE HEAD END OF THE STRETCHER WAS BENT AND THE ROCKER ARM SLIPPING. THE TECH REPLACED THE HEX ROD AND RECONNECTED THE ROCKER ARM TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE BRAKES WOULD SET AND HOLD AT THE FOOT END OF THE STRETCHER BUT NOT HOLD AT THE HEAD END.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1