BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GPS PROCEDURAL STRETCHER

    MDR report key: 1812878 · Received August 12, 2010

    Report

    Report Number
    1824206-2010-09289
    Event Type
    Malfunction
    Date Received
    August 12, 2010
    Date of Event
    July 20, 2010
    Report Date
    July 20, 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 FOUND THE RIVET ON THE TRANSFER LINK AT THE HEAD END OF THE STRETCHER CAME OFF. THE TECHNICIAN REPLACED THE RIVET TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE HEAD END CASTERS ARE NOT HOLDING WHEN THE BRAKE IS APPLIED AT THE FOOT END OF THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GPS PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 883

    Patients

    Seq Age Sex Outcome Treatment
    1