BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2160549 · Received July 6, 2011

    Report

    Report Number
    1824206-2011-03573
    Event Type
    Malfunction
    Date Received
    July 6, 2011
    Date of Event
    June 24, 2011
    Report Date
    June 24, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE BED IN ED. ALL FOUR CASTERS WERE FAULTY AND COULD SWIVEL IN BRAKE POSITION. REPLACED ALL FOUR CASTERS TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT ALL 4 BRAKE CASTERS SWIVEL WHEN IN BRAKE POSITION. NO INJURY ALLEGED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1