BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 1193378 · Received October 7, 2008

    Report

    Report Number
    1824206-2008-03720
    Event Type
    Malfunction
    Date Received
    October 7, 2008
    Date of Event
    September 11, 2008
    Report Date
    September 11, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE FACILITIES MAINTENANCE FOUND THE RIGHT OUTSIDE SIDERAIL SWITCH PACKAGE MALFUNCTIONED CAUSING THE UNINTENTIONAL MOVEMENT. THE SWITCH PACKAGE WAS REPLACED TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD SECTION FUNCTION OF THE BED RAISED UNINTENTIONALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1155

    Patients

    Seq Age Sex Outcome Treatment
    1