BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3950192 · Received June 27, 2014

    Report

    Report Number
    1627487-2014-26442
    Event Type
    Injury
    Date Received
    June 27, 2014
    Date of Event
    February 19, 2014
    Report Date
    May 5, 2014
    Manufacturer
    ST. JUDE MEDICAL -NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-07262012-002-R
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY. 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 HAS NOT CHARGED HIS SCS SYSTEM IN OVER 2-3 MONTHS HENCE, THE IPG IS UNABLE TO COMMUNICATE WITH THE PROGRAMMER OR CHARGER. THE PATIENT IS NO LONGER RECEIVING STIMULATION. FOLLOW UP INFORMATION IDENTIFIED THE PATIENT UNDERWENT A SURGICAL PROCEDURE TO REPLACE THE IPG. THE PATIENT IS NOW RECEIVING EFFECTIVE STIMULATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    376662 EON MINI SCS IPG GZB ST. JUDE MEDICAL -NEUROMODULATION 3788 3326584

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Other SCS LEAD, MODEL: 3228| IMPLANT DATE: