BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3931414 · Received June 26, 2014

    Report

    Report Number
    1627487-2014-02465
    Event Type
    Injury
    Date Received
    June 26, 2014
    Date of Event
    March 4, 2014
    Report Date
    June 3, 2014
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

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

    Description of Event or Problem · 1

    DEVICE 1 OF 2. REFERENCE MFR REPORT: 1627487-2014-02466. THE PT RECEIVED TWO SCS LEADS FROM THE LEAD LOT NUMBER. IT WAS REPORTED THE PT EXPERIENCED PERSISTENT BURNING AT HIS SCS IPG SITE. THE PT STATED HE ALLOWED THE BATTERY TO DEPLETE AND THE BURNING SUBSIDED. IN ADDITION, THE PT COMPLAINED HIS STIMULATION WAS NOT HELPING HIM ANYMORE. THE PT'S ENTIRE SCS SYS WAS REMOVED ON (B)(6) 2014.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    373158 EON MINI SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3956062

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other SCS ANCHOR, MODEL 1192 (X2)| IMPLANT DATE: