BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GPS PROCEDURAL STRETCHER

    MDR report key: 2113203 · Received May 24, 2011

    Report

    Report Number
    1824206-2011-02901
    Event Type
    Malfunction
    Date Received
    May 24, 2011
    Date of Event
    March 14, 2011
    Report Date
    March 14, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE TRANS LINK WAS BROKEN. HE REPLACED THE TRANS LINK TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE CASTERS ARE NOT HOLDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GPS PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 881

    Patients

    Seq Age Sex Outcome Treatment
    1