BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE

    MDR report key: 3223807 · Received July 10, 2013

    Report

    Report Number
    1627487-2013-11010
    Event Type
    Injury
    Date Received
    July 10, 2013
    Date of Event
    June 18, 2013
    Report Date
    June 18, 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 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

    ON (B)(6) 2013, THE PATIENT UNDERWENT A TRIAL PROCEDURE AND WAS IMPLANTED WITH TWO LEADS FROM THE SAME LOT. DURING THE PROCEDURE, THE PATIENT EXPERIENCED A SHOCKING SENSATION FROM HIS LEGS TO HIS FEET WHEN THE SECOND LEAD WAS PLACED. IN RECOVERY, THE PATIENT EXPERIENCED TINGLING PAIN IN HIS FEET. AS A RESULT, THE PATIENT WAS PRESCRIBED PAIN MEDICATION AND NEURONTIN. THE TRIAL LEADS WERE REMOVED ON (B)(6) 2013. OVER TIME, THE TINGLING PAIN HAS DIMINISHED. PER THE DOCTOR'S REQUEST, THE PATIENT WILL REMAIN ON NEURONTIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    314788 OCTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3086 4038909

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Other