BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE

    MDR report key: 2921948 · Received January 4, 2013

    Report

    Report Number
    1627487-2013-05054
    Event Type
    Injury
    Date Received
    January 4, 2013
    Date of Event
    December 10, 2012
    Report Date
    December 11, 2012
    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 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

    THE PATIENT UNDERWENT A TRIAL PROCEDURE ON (B)(6) 2012. DURING THE PROCEDURE, THE DOCTOR EXPERIENCED DIFFICULTY PLACING THE LEAD DUE TO THE PATIENT HAVING SCOLIOSIS. POST-OP, THE PATIENT WAS UNABLE TO RECEIVE ADEQUATE COVERAGE. REPROGRAMMING WAS UNSUCCESSFUL. X-RAYS REVEALED THE LEAD HAD MIGRATED. AS A RESULT, THE DOCTOR REMOVED THE LEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    5440 OCTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3086 3832203

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention