BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMITRODE 44 LEAD

    MDR report key: 1604686 · Received February 5, 2010

    Report

    Report Number
    1627487-2010-00003
    Event Type
    Injury
    Date Received
    February 5, 2010
    Date of Event
    January 5, 2010
    Report Date
    January 6, 2010
    Manufacturer
    ADVANCED NEUROMODULATION SYSTEMS, INC.
    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

    DEVICE HISTORY AND STERILIZATION RECORDS WERE REVIEWED. RESULTS: THE DEVICE HISTORY AND STERILIZATION RECORDS REVIEWED WERE FOUND TO MEET SPECIFICATIONS AND NO ANOMALIES WERE FOUND. CONCLUSION: THE CAUSE OF THE REPORTED COMPLIANT COULD NOT BE DETERMINED FROM THE REVIEW OF THE DHR AND STERILIZATION RECORDS. ANS 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. ANS DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED SKIN EROSION AT THE PADDLE IMPLANT SITE. THE PHYSICIAN CLEANED THE WOUND AND SENT THE PATIENT HOME WITH ANTIBIOTIC THERAPY. AS OF (B) (6) 2009 PATIENT IS REPORTED TO BE DOING WELL. SYSTEM WAS NOT EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LAMITRODE 44 LEAD SPINAL CORD STIMULATION LEAD LGW ADVANCED NEUROMODULATION SYSTEMS, INC. 3262 2838254

    Patients

    Seq Age Sex Outcome Treatment
    1 Other