BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 1821807 · Received August 26, 2010

    Report

    Report Number
    1824206-2010-09599
    Event Type
    Malfunction
    Date Received
    August 26, 2010
    Date of Event
    August 3, 2010
    Report Date
    August 3, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE CONTROL BOX AND NOW HEAD WILL NOT WORK AT ALL. THE ACCOUNT HAS A LOCKOUT BOX FROM ANOTHER BED THEY WILL INSTALL. REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD MOTOR WILL WORK UP BUT NOT DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESIDENT BED AC POWERED HOSPITAL BED FNL HILL-ROM INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1