BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1964512 · Received December 22, 2010

    Report

    Report Number
    1824206-2010-11888
    Event Type
    Malfunction
    Date Received
    December 22, 2010
    Date of Event
    November 23, 2010
    Report Date
    November 23, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN USED A BRAKE/STEER UPGRADE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE BRAKE IS NOT WORKING ON THE STRETCHER.

    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