BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA TRANSTAR STRETCHER

    MDR report key: 2181983 · Received February 4, 2011

    Report

    Report Number
    1824206-2011-00670
    Event Type
    Malfunction
    Date Received
    February 4, 2011
    Date of Event
    January 12, 2011
    Report Date
    January 12, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE FOOT SECTION CASTERS TO CORRECT THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD SECTION CASTERS WILL LOCK IN BRAKE BUT THE FOOT SECTION CASTERS WILL NOT LOCK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRAUMA TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8040

    Patients

    Seq Age Sex Outcome Treatment
    1