BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMITRODE S8

    MDR report key: 2861085 · Received December 4, 2012

    Report

    Report Number
    1627487-2012-12711
    Event Type
    Injury
    Date Received
    December 4, 2012
    Date of Event
    September 21, 2012
    Report Date
    November 13, 2012
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Adverse Event
    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 PT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 2 OF 3. REFERENCE MFR REPORT #1627487-2012-12710, 12712. IT WAS REPORTED THE PT DEVELOPED A NEW PAIN PATTERN THAT COULD NOT BE CAPTURED WITH CURRENT LEAD PLACEMENT. THE PHYSICIAN OFFERED TO ADD ANOTHER LEAD TO CAPTURE THE NEW PAIN. REPORTEDLY THE PT OPTED TO HAVE COMPLETE SYSTEM EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LAMITRODE S8 SCS LEAD GZB ST. JUDE MEDICAL - NEUROMODULATION 3286 3456429

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention SCS ANCHOR: MODEL 1192| IMPLANT DATE: