BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HILL-ROM 100 LOW BED

    MDR report key: 2191786 · Received July 28, 2011

    Report

    Report Number
    1824206-2011-04001
    Event Type
    Malfunction
    Date Received
    July 28, 2011
    Date of Event
    July 7, 2011
    Report Date
    July 7, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICAL SUPPORT SENT THE ACCOUNT A BATTERY CABLE. THE ACCOUNT HAS NOT RETURNED HILL-ROM'S ATTEMPTS TO DETERMINE THE RESOLUTION OF THE ALLEGED MALFUNCTION.

    Description of Event or Problem · 1

    THE ACCOUNTS MAINTENANCE STATED THAT THE HEAD OF THE BED WILL NOT LOWER. HE HAS TRIED ANOTHER PENDANT, ISOLATED THE PENDANT EXTENSION CABLE SWITCHED THE HEAD AND KNEE MOTORS AND REPLACED THE CONTROL BOX BUT THE ISSUE REMAINS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HILL-ROM 100 LOW BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3930

    Patients

    Seq Age Sex Outcome Treatment
    1