BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCTRODE

    MDR report key: 2980007 · Received February 22, 2013

    Report

    Report Number
    1627487-2013-01191
    Event Type
    Injury
    Date Received
    February 22, 2013
    Date of Event
    October 31, 2008
    Report Date
    January 28, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    METHOD: THE DEVICE HISTORY AND STERILIZATION RECORDS WERE REVIEWED. RESULTS: THE DEVICE HISTORY AND STERILIZATION RECORDS REVIEWED WERE FOUND TO MEET SPECIFICATIONS AND NO ANOMALIES RELATED TO THIS EVENT WERE FOUND. CONCLUSION: THE CAUSE OF THE REPORTED COMPLAINT COULD NOT BE DETERMINED FROM THE REVIEW OF THE DHR AND STERILIZATION RECORDS. 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 3 OF 3. REFERENCE MFR REPORT: 1627487-2013-1189. REFERENCE MFR REPORT: 1627487-2013-1190. IT WAS REPORTED THE PATIENT'S ENTIRE SCS SYSTEM WAS REMOVED APPROXIMATELY 6 WEEKS AFTER IMPLANT DUE TO A PSEUDOMONAS INFECTION. IT IS UNKNOWN WHERE THE INFECTION SITE WAS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    78877 OCTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3186 116490

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Required Intervention