BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GPS PROCEDURAL STRETCHE

    MDR report key: 2222919 · Received July 15, 2011

    Report

    Report Number
    1824206-2011-03749
    Event Type
    Malfunction
    Date Received
    July 15, 2011
    Date of Event
    June 29, 2011
    Report Date
    June 29, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE FOUR CASTERS TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE TECH REPLACED THE FOUR CASTERS TO REPAIR THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GPS PROCEDURAL STRETCHE WHEELED STRETCHER FPO HILL-ROM, INC. 886

    Patients

    Seq Age Sex Outcome Treatment
    1