BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DURASTAR STRETCHER

    MDR report key: 2010261 · Received March 1, 2011

    Report

    Report Number
    1824206-2011-01205
    Event Type
    Malfunction
    Date Received
    March 1, 2011
    Date of Event
    February 7, 2011
    Report Date
    February 7, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED WHEN THEY LOCK THE BRAKE/STEER CASTERS INTO BRAKE, THE HEAD END CASTERS DO NOT HOLD, BUT THE FOOT END CASTERS DO HOLD. HE REVERSED THE LINKAGE AT THE FOOT END AND THE ISSUE RETURNED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DURASTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8005

    Patients

    Seq Age Sex Outcome Treatment
    1