BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1111970 · Received August 12, 2008

    Report

    Report Number
    1824206-2008-03046
    Event Type
    Malfunction
    Date Received
    August 12, 2008
    Date of Event
    September 19, 2007
    Report Date
    September 19, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    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 SET SCREWS IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    THE BRAKES ON THIS STRETCHER WOULD NOT HOLD WHEN APPLIED.

    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