BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    JERON NURSE CALL SYSTEM, MODEL PROVIDER 680

    MDR report key: 165114 · Received April 28, 1998

    Report

    Report Number
    165114
    Event Type
    Malfunction
    Date Received
    April 28, 1998
    Date of Event
    April 13, 1998
    Report Date
    April 23, 1998
    Manufacturer
    JERON ELECTRONIC SYSTEM, 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 INDICATE THE ROOM NUMBER OF A CODE. IT INDICATED THE FLOOR, NOT THE ROOM NUMBER. THE CODE-BLUE ALARM WORKED ON THE FLOOR THAT THE CODE WAS ON. THIS PREVENTED THE CODE TEAM FROM RESPONDING. THE NURSES ON THE FLOOR SUCCESSFULLY REVIVED THE PT. WITH NO FURTHER COMPLICATIONS. THE MFR RE-CONFIGURED THE SOFTWARE AND THE SYSTEM IS NOW FULLY FUNCTIONAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JERON NURSE CALL SYSTEM, MODEL PROVIDER 680 NURSE CALL SYSTEM ILQ JERON ELECTRONIC SYSTEM, INC. PROVIDER 680 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other