BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2800325 · Received October 9, 2012

    Report

    Report Number
    1824206-2012-06257
    Event Type
    Malfunction
    Date Received
    October 9, 2012
    Date of Event
    July 30, 2012
    Report Date
    July 30, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THAT THE BRAKE WOULD SET BUT THE CASTERS CONTINUED TO SWIVEL FROM SIDE TO SIDE IF YOU PUSHED ON STRETCHER. THE CASTER WHEEL WOULD NOT ROLL. THE TECHNICIAN REPLACED THE FOUR BRAKE CASTERS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE COMPLAINANT STATED THE BRAKE IS COMING UNLATCHED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1