BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2232665 · Received July 19, 2011

    Report

    Report Number
    1824206-2011-03804
    Event Type
    Malfunction
    Date Received
    July 19, 2011
    Date of Event
    June 27, 2011
    Report Date
    June 27, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE PIVOT SLIDES; EXTRUSIONS AND THE SUPPORT ARMS ON BOTH SIDES OF THE HEAD SECTION WERE DETACHED. HE REPLACED THE PIVOT SLIDES, EXTRUSIONS AND REATTACHED THE SUPPORT ARMS TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE HEAD OF THE BED CANNOT BE RAISED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1