BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3820987 · Received May 8, 2014

    Report

    Report Number
    1627487-2014-21296
    Event Type
    Injury
    Date Received
    May 8, 2014
    Date of Event
    April 17, 2014
    Report Date
    April 17, 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
    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 HAS NOT USED HER SCS SYSTEM FOR 3-4 WKS SINCE SHE DID NOT HAVE BACK PAIN AT THE TIME. THE PT HAD NOT CHARGED THE IPG FOR APPROX TWO MONTHS. THE SJM REP WAS UNABLE TO ESTABLISH COMMUNICATION USING MULTIPLE EXTERNAL DEVICES. SURGICAL INTERVENTION WILL BE TAKEN TO ADDRESS THE IPG ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    279148 EON MINI SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3972239

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Other IMPLANT DATE:| SCS LEAD: MODEL 3228