BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON

    MDR report key: 3810571 · Received May 6, 2014

    Report

    Report Number
    1627487-2014-26387
    Event Type
    Injury
    Date Received
    May 6, 2014
    Date of Event
    April 15, 2014
    Report Date
    April 15, 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 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 PT WAS NOT RECEIVING STIMULATION. IT WAS NOTED THE PT DID NOT CHARGE HER IPG. THE PT'S IPG WAS EXPLANTED AND REPLACED WHICH RESOLVED THE ISSUE. EFFECTIVE STIMULATION WAS RESTORED FOLLOWING THE PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271584 EON SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3716 57062

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR Other IMPLANT DATE:| SCS LEAD, MODEL 3186