BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PENTA

    MDR report key: 3182139 · Received June 14, 2013

    Report

    Report Number
    1627487-2013-06476
    Event Type
    Injury
    Date Received
    June 14, 2013
    Date of Event
    May 2, 2013
    Report Date
    May 21, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    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 INFO 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

    IT WAS REPORTED THE PT IS NOT RECEIVING EFFECTIVE PAIN RELIEF. THE PT HAS BEEN REPROGRAMMED MULTIPLE TIMES UNSUCCESSFULLY. THE PT'S PHYSICIAN BELIEVES THE SYSTEM IS HELPING THE PT. THE PT WAS REPROGRAMMED AND WILL CONTINUE TO USE HIS SYSTEM AND EVALUATED WHETHER HE WANTS TO HAVE IT REMOVED IN THE FUTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    270995 PENTA SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3228 3593621

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Other SCS IPG: MODEL 3788| IMPLANTED: