BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 1132383 · Received August 22, 2008

    Report

    Report Number
    1824206-2008-03175
    Event Type
    Malfunction
    Date Received
    August 22, 2008
    Date of Event
    July 24, 2008
    Report Date
    July 24, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL MAINTENANCE PERSON REPORTED THAT THE BED EXIT ALARM WOULD NOT FUNCTION ON THIS BED. HE FOUND THAT THE POSITION SENSOR TAPE SWITCHES WERE DEFECTIVE. HE REPLACED THE TAPE SWITCHES AND BED FUNCTIONED AS DESIGNED. HE STATED THAT THERE WERE NO REPORTED ADVERSE EVENTS ASSOCIATED WITH THIS BED MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1115 NA

    Patients

    Seq Age Sex Outcome Treatment
    1