BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON

    MDR report key: 3082453 · Received April 16, 2013

    Report

    Report Number
    1627487-2013-01433
    Event Type
    Injury
    Date Received
    April 16, 2013
    Date of Event
    March 26, 2013
    Report Date
    March 26, 2013
    Manufacturer
    ST. JUDE MEDICAL, NEUROMODULATION
    Product Code
    LGW
    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

    DEVICE 1 OF 3. REFERENCE MFR REPORT: 1627487-2013-1434. REFERENCE MFR REPORT: 1627487-2013-1435. IT WAS REPORTED, THE PATIENT HAS EXPERIENCING A SHOCKING SENSATION AT THE IPG SITE 6 TO 8 TIMES SINCE (B)(6) 2012. HIS PHYSICIAN INDICATED THIS PAIN IS DUE TO THE IPG IMPLANT DEPTH AND LOCATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    163826 EON SCS IPG LGW ST. JUDE MEDICAL, NEUROMODULATION 3716 174089

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Required Intervention