BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NUCLEUS CI24 RCS

    MDR report key: 526402 · Received May 7, 2004

    Report

    Report Number
    MW1032041
    Event Type
    Injury
    Date Received
    May 7, 2004
    Date of Event
    April 30, 2004
    Report Date
    May 7, 2004
    Manufacturer
    COCHLEAR LTD
    Product Code
    MCM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    IN 2004 COCHLEAR IMPLANT INTERNAL DEVICE FAILURE DETECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NUCLEUS CI24 RCS COCHLEAR IMPLANTS MCM COCHLEAR LTD CI24RCS *

    Patients

    Seq Age Sex Outcome Treatment
    1 25 MO Required Intervention