BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA

    MDR report key: 1757039 · Received July 1, 2010

    Report

    Report Number
    1824206-2010-08585
    Event Type
    Malfunction
    Date Received
    July 1, 2010
    Date of Event
    June 9, 2010
    Report Date
    June 9, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED A BED IN STORAGE HAD NO TRENDELENBURG/REV TREND FUNCTIONS. HE REPLACED POWER SUPPLY BOARD, AND ADJUSTED TREND ENGAGE SWITCH, AND FOUND A SHORTED WIRE ON POWER LIMIT CABLE. ACCOUNT DECIDED TO SCRAP THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P850

    Patients

    Seq Age Sex Outcome Treatment
    1