BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2931414 · Received November 13, 2012

    Report

    Report Number
    1824206-2012-07392
    Event Type
    Malfunction
    Date Received
    November 13, 2012
    Date of Event
    November 30, 2009
    Report Date
    November 30, 2009
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE COMPLAINANT STATED THAT THE BED WAS ENERGIZED WHEN IT WAS PLUGGED INTO THE WALL. THE PATIENT AND NURSE RECEIVED AN ELECTRIC SHOCK.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK