BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA BED

    MDR report key: 2130333 · Received May 9, 2011

    Report

    Report Number
    1824206-2011-02602
    Event Type
    Malfunction
    Date Received
    May 9, 2011
    Date of Event
    April 14, 2011
    Report Date
    April 14, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE RED CABLE AND THE LOGIC BOARD AND THE ISSUE REMAINS. HE SAID THE HI/LOW WORKS FINE IF THE HEAD SECTION IS ABOVE 45 DEGREES. THE ACCOUNT DECIDED TO SCRAP THE BED DECLINED TO REPAIR.

    Description of Event or Problem · 1

    THE ACCOUNT STATED WHEN LOWERING THE HI/LOW, THE BED WILL REVERSE ITSELF AND RUN UP A FEW INCHES. THIS OCCURS ABOUT A FOOT ABOVE THE LOW LIMIT. THE BED HAS BEEN IN THE BED SHOP FOR ABOUT TWO MONTHS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1600

    Patients

    Seq Age Sex Outcome Treatment
    1