BEUDAMED
    FDA Adverse Event Injury Summary report: N

    JERON 700/790 NURSE CALL

    MDR report key: 20399707 · Received October 7, 2024

    Report

    Report Number
    MW5160801
    Event Type
    Injury
    Date Received
    October 7, 2024
    Report Date
    October 2, 2024
    Manufacturer
    JERON ELECTRONIC SYSTEMS INC.
    Product Code
    ILQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    CONTINUED ISSUES WITH NURSE CALL EQUIPMENT IN AT LEAST 30 VARIOUS LOCATIONS IN ACUTE CARE HOSPITALS THRU OUT THE US AND CANADA. NO TESTING WAS COMPLETED MOST EQUIPMENT WAS REPLACED AT LEAST ONCE MAYBE TWICE AND IN SOME CASES 4 TIMES WITH AT LEAST 4 CODES NOT BEING ANNUNCIATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2005508 JERON 700/790 NURSE CALL SYSTEM, COMMUNICATION, POWERED ILQ JERON ELECTRONIC SYSTEMS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other| L