BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1082758 · Received July 23, 2008

    Report

    Report Number
    1824206-2008-02874
    Event Type
    Malfunction
    Date Received
    July 23, 2008
    Date of Event
    July 9, 2008
    Report Date
    July 9, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A HILL-ROM TECHNICIAN DETERMINED THE LOGIC BOARD WAS THE CAUSE OF THE UNINTENTIONAL MOVEMENT. HE REPLACED THE LOGIC BOARD AND THE BED FUNCTIONED PROPERLY.

    Description of Event or Problem · 1

    BED HAD UNEXPECTED MOTION. AFTER LOWERING BED, WOULD COME BACK UP AUTOMATICALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200

    Patients

    Seq Age Sex Outcome Treatment
    1