BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2010025 · Received March 2, 2011

    Report

    Report Number
    1824206-2011-01222
    Event Type
    Malfunction
    Date Received
    March 2, 2011
    Date of Event
    February 8, 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

    THE TECHNICIAN REPLACED BOTH HEX RODS AND SCREWS TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BRAKE AND STEER ARE NOT ENGAGING DUE TO BROKEN SCREWS IN THE HEX ROD AT BOTH ENDS OF THE STRETCHER.

    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