BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE PERCUTANEOUS LEAD

    MDR report key: 2023355 · Received March 16, 2011

    Report

    Report Number
    1627487-2011-01251
    Event Type
    Injury
    Date Received
    March 16, 2011
    Date of Event
    February 14, 2011
    Report Date
    February 14, 2011
    Manufacturer
    ST JUDE MEDICAL - NEUROMODULATION DIVISION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, 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 2. REFERENCE MANUFACTURER REPORT: 1627487-2011-01252. THE PATIENT RECEIVED AN SCS SYSTEM, INCLUDING AN IPG AND THREE PERCUTANEOUS LEADS (FROM TWO SEPARATE LOTS), ON (B)(6) 2008. IT WAS REPORTED THAT THE LEADS WERE IMPLANTED AT T10 AND T11 DUE TO THE PATIENT'S PAIN PATTERN. THE PATIENT STATED HE FELT UNCOMFORTABLE STIMULATION IN THE ABDOMEN AND RIBS AT ALL ELECTRODE LOCATIONS. THE PHYSICIAN EXPLANTED THE PATIENT'S SYSTEM ON (B)(6) 2011. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OCTRODE PERCUTANEOUS LEAD SPINAL CORD STIMULATION LEAD LGW ST JUDE MEDICAL - NEUROMODULATION DIVISION 3186 173576

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Required Intervention