BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1162752 · Received September 8, 2008

    Report

    Report Number
    1824206-2008-03308
    Event Type
    Malfunction
    Date Received
    September 8, 2008
    Date of Event
    August 25, 2008
    Report Date
    August 25, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE BRAKES NOT HOLDING/WORKING COULD LEAD TO UNINTENTIONAL MOVEMENT OF THE STRETCHER, WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE CASTERS IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    IT WAS DISCOVERED THAT THE FOOT END BRAKES ON THIS STRETCHER WOULD NOT FUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P8000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1