BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCED BED

    MDR report key: 1122223 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-03130
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 16, 2008
    Report Date
    July 16, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HILL-ROM TECHNICIAN REPORTED THAT THE BED EXIT ALARM SYSTEM DID NOT FUNCTION ON THIS BED. HE FOUND THAT THE BED EXIT TAPE SWITCHES WERE DEFECTIVE. HE REPLACED THE SWITCHES AND THE BED EXIT SYSTEM FUNCTIONED AS DESIGNED. THERE WERE NO REPORTED ADVERSE EVENTS ASSOCIATED WITH THIS PRODUCT MALFUNCTION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1