BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 1162848 · Received September 9, 2008

    Report

    Report Number
    1824206-2008-03339
    Event Type
    Malfunction
    Date Received
    September 9, 2008
    Date of Event
    August 13, 2008
    Report Date
    August 13, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL BIOMED REPORTED THAT THE BED EXIT ALARM SYSTEM DID NOT FUNCTION ON THIS BED. AFTER TROUBLESHOOTING WITH A HILL-ROM TECHNICIAN IT WAS 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 ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1155 NA

    Patients

    Seq Age Sex Outcome Treatment
    1