BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GPS PROCEDURAL STRETCHER

    MDR report key: 1905677 · Received November 12, 2010

    Report

    Report Number
    1824206-2010-10987
    Event Type
    Malfunction
    Date Received
    November 12, 2010
    Date of Event
    October 19, 2010
    Report Date
    October 19, 2010
    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 REPLACED THE TREND CYLINDERS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE STRETCHER IS NOT GOING INTO TRENDELENBURG OR REVERSE TRENDELENBURG.

    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