BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DURASTAR STRETCHER

    MDR report key: 1894071 · Received November 4, 2010

    Report

    Report Number
    1824206-2010-10871
    Event Type
    Malfunction
    Date Received
    November 4, 2010
    Date of Event
    October 11, 2010
    Report Date
    October 11, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE GAS SPRINGS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD OF THE BED IS NOT STAYING UP DUE TO THE GAS SPRINGS NOT HOLDING THE POSITION.

    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