BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3851393 · Received May 22, 2014

    Report

    Report Number
    1627487-2014-00307
    Event Type
    Injury
    Date Received
    May 22, 2014
    Date of Event
    April 29, 2014
    Report Date
    April 29, 2014
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    IT WAS REPORTED THE PATIENT ((B)(6)) IS EXPERIENCING SORENESS AT THE IPG SITE. IN ADDITION, THE IPG IS REPORTEDLY PROTRUDING. DETAILS REGARDING THE COURSE OF ACTION FOR THIS MATTER HAVE NOT BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    306750 EON MINI SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3869050

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other SCS LEAD, MODEL: 3189 (2)| IMPLANT DATE: