BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1062159 · Received June 13, 2008

    Report

    Report Number
    1824206-2008-02666
    Event Type
    Malfunction
    Date Received
    June 13, 2008
    Date of Event
    March 6, 2008
    Report Date
    March 6, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

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

    Description of Event or Problem · 1

    BRAKES WOULD NOT WORK ON THE HEAD END OF THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P8005 NA

    Patients

    Seq Age Sex Outcome Treatment
    1