BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE

    MDR report key: 3032306 · Received March 29, 2013

    Report

    Report Number
    1627487-2013-01371
    Event Type
    Injury
    Date Received
    March 29, 2013
    Date of Event
    March 8, 2013
    Report Date
    March 8, 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 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

    IT WAS REPORTED DURING A PERMANENT IMPLANT PROCEDURE, ONE LEAD SHOWED IMPEDANCE ISSUES. THE PHYSICIAN REPLACED THE LEAD WITH A NEW ONE. THE PROCEDURE WAS EXTENDED 30 MINUTES. THE PT IS RECEIVING EFFECTIVE STIMULATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    130108 OCTRODE SCS LEAD LGW ST JUDE MEDICAL - NEUROMODULATION 3186 3918814

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Required Intervention