BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GPS PROCEDURAL STRETCHER

    MDR report key: 1070494 · Received July 1, 2008

    Report

    Report Number
    1824206-2008-02778
    Event Type
    Malfunction
    Date Received
    July 1, 2008
    Date of Event
    June 15, 2008
    Report Date
    June 15, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT FALSE LATCHING OR NO LATCHING OF SIDERAILS COULD RESULT IN SERIOUS INJURY, AND THEREFORE THIS EVENT WILL BE REPORTED.

    Description of Event or Problem · 1

    STRETCHER SIDERAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GPS PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P883 NA

    Patients

    Seq Age Sex Outcome Treatment
    1