BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    JERON NURSE CALL SYSTEM, MODEL 860

    MDR report key: 72821 · Received February 28, 1997

    Report

    Report Number
    72821
    Event Type
    Malfunction
    Date Received
    February 28, 1997
    Date of Event
    February 21, 1997
    Report Date
    February 27, 1997
    Manufacturer
    JERON ELECTRONIC SYSTEMS, INC.
    Product Code
    ILQ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CODE-BLUE ALARM MONITORED BY OPERATORS FAILED TO ALARM DURING A CODE ON ONE FLOOR. THIS PREVENTED THE OPERATORS FROM ANNOUNCING THE CODE ON THE OVERHEAD PAGER. THE CODE-BLUE ALARMS WORKED ON THE FLOOR THAT THE CODE WAS ON, ONLY THE OPERATORS DID NOT RECEIVE THE CODE. CPR WAS SUCCESSFULLY INITIATED AND THE PT SURVIVED. THE SYSTEM HUB WAS REBOOTED AND SOFTWARE WAS RELOADED TO THAT TOWER SYSTEM. THE SYSTEM IS NOW FULLY FUNCTONAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JERON NURSE CALL SYSTEM, MODEL 860 NURSE CALL SYSTEM ILQ JERON ELECTRONIC SYSTEMS, INC. SYSTEM 860, CONSOLE 6865 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN