BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE LEAD

    MDR report key: 2133584 · Received June 16, 2011

    Report

    Report Number
    1627487-2011-02825
    Event Type
    Injury
    Date Received
    June 16, 2011
    Date of Event
    May 19, 2011
    Report Date
    May 19, 2011
    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 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 # 1627487-2011-02826. THE PT WAS IMPLANTED WITH AN SCS SYSTEM. IT WAS REPORTED THAT HE WAS NOT RECEIVING STIMULATION IN THE PREDOMINANT AREA OF HIS PAIN. THE SCS SYSTEM WAS REVISED ON (B)(6) 2011. AFTER THE REVISION, THE PT WAS RECEIVING BETTER STIMULATION COVERAGE. NO ADDITIONAL INFO IS KNOWN AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OCTRODE LEAD SPINAL CORD STIMULATION LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3186 3221975

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Required Intervention IMPLANTED:| IPG: MODEL 3716