BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE

    MDR report key: 3122126 · Received May 17, 2013

    Report

    Report Number
    1627487-2013-05697
    Event Type
    Injury
    Date Received
    May 17, 2013
    Date of Event
    February 4, 2013
    Report Date
    April 23, 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 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

    DEVICE 1 OF 2. REFERENCE MFR REPORT#: 1627487-2013-05698. THE PT HAS TWO LEADS FROM THE SAME LOT. IT WAS REPORTED THE PT EXPERIENCES OVERSTIMULATION AT THE IPG AND LEAD SITE. AS A RESULT, THE PT WAS ADVISED TO DEACTIVATE STIMULATION. THE PT WAS PLACED BACK ON PAIN MEDICATION AND WILL FOLLOW-UP WITH HER DOCTOR AND/OR SJM REPRESENTATIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    219678 OCTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3186 3817704

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Required Intervention SCS ANCHORS: MODEL 1192 (X2)| IMPLANTED: