BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3 MOTOR ADVANCE BED

    MDR report key: 2011771 · Received February 9, 2011

    Report

    Report Number
    1824206-2011-00774
    Event Type
    Malfunction
    Date Received
    February 9, 2011
    Date of Event
    January 18, 2011
    Report Date
    January 18, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE LIMIT SWITCH WAS OUT OF ADJUSTMENT. HE ADJUSTED THE UP AND DOWN LIMITS TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BED WILL NOT GO INTO TRENDELENBURG OR REVERSE TRENDELENBURG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 3 MOTOR ADVANCE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1140

    Patients

    Seq Age Sex Outcome Treatment
    1