BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3960159 · Received July 23, 2014

    Report

    Report Number
    1627487-2014-24049
    Event Type
    Injury
    Date Received
    July 23, 2014
    Date of Event
    July 1, 2014
    Report Date
    July 1, 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
    GA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFO 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

    THE PT REPORTED THAT HE LAST USED HIS IPG APPROXIMATELY A MONTH AGO, AND IS CURRENTLY UNABLE TO COMMUNICATE WITH THE IPG USING THE CHARGING SYSTEM AND THE PROGRAMMER. THE PT DOES NOT HAVE STIMULATION. SURGICAL INTERVENTION TOOK PLACE ON (B)(6) 2014 TO REPLACE THE PT'S SCS IPG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    429809 EON MINI SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3724386

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Other SCS LEAD: MODEL 3228| IMPLANT DATE: