BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    REMANUFACTURED BED

    MDR report key: 1890718 · Received November 1, 2010

    Report

    Report Number
    1824206-2010-10783
    Event Type
    Malfunction
    Date Received
    November 1, 2010
    Date of Event
    October 6, 2010
    Report Date
    October 6, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE CONTROL BOARD WAS NOT FUNCTIONING. THE TECHNICIAN REPLACED THE CONTROL BOARD TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED, THE BED HAS NO POWER. THE BED IS NOT EQUIPPED WITH CPR AND THE HEAD IS STUCK IN THE RAISED POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REMANUFACTURED BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8400

    Patients

    Seq Age Sex Outcome Treatment
    1