BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 4092129 · Received September 3, 2014

    Report

    Report Number
    1627487-2014-01562
    Event Type
    Injury
    Date Received
    September 3, 2014
    Date of Event
    August 1, 2013
    Report Date
    August 11, 2014
    Manufacturer
    ST. JUDE MEDICAL ¿ NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Adverse Event
    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 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 EXPERIENCED PERSISTENT PAIN AT THE IPG SITE FOR THE PAST ONE YEAR. REPORTEDLY, THE PAIN HAD DECREASED SINCE THAT TIME AND THEREFORE THE PATIENT DISCONTINUED USE OF THE SYSTEM. SURGICAL INTERVENTION MAY BE UNDERTAKEN AS THE NEXT COURSE OF ACTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    535375 EON MINI SCS IPG GZB ST. JUDE MEDICAL ¿ NEUROMODULATION 3788 3199512

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Other SCS LEAD, MODEL: 3219| IMPLANT: