BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 4223273 · Received October 29, 2014

    Report

    Report Number
    1627487-2014-20385
    Event Type
    Injury
    Date Received
    October 29, 2014
    Date of Event
    July 9, 2014
    Report Date
    October 9, 2014
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-12192011-003-R
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    CORRECTION NUMBERS: 1627487-07262012-002-R, 1627487-05242011-002-R. THIS IPG SERIAL NUMBER WAS INCLUDED IN FIELD ADVISORIES. SJM HAS LIMITED INFO 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. UDI(DI): (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THE PATIENT'S IPG BECAME INOPERABLE DUE TO NOT CHARGING IT FOR ABOUT 3 MONTHS. THE SJM REP CONFIRMED THE COMMUNICATION ISSUE BETWEEN IPG AND MULTIPLE EXTERNAL DEVICES. SURGICAL INTERVENTION WILL BE TAKEN AT A LATER TO ADDRESS THE ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    691132 EON MINI SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3166349

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other IMPLANT DATE:| SCS LEAD, MODEL: 3228,