BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3252160 · Received July 25, 2013

    Report

    Report Number
    1627487-2013-06672
    Event Type
    Injury
    Date Received
    July 25, 2013
    Date of Event
    June 28, 2013
    Report Date
    June 28, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    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 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

    IT WAS REPORTED THE PT EXPERIENCED PAIN AT HER IPG SITE. THE PT WAS PRESCRIBED LIDOCAINE AND THE ISSUE HAD ALLEGEDLY RESOLVED, HOWEVER, THE PT WILL HAVE HER IPG REMOVED. FOLLOW-UP IDENTIFIED THE PT HAD HER IPG EXPLANTED ON (B)(6) 2013. THE ISSUE IS RESOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    349272 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3760299

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Other IMPLANTED:| SCS LEAD: MODEL 3219