BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMITRODE TRIPOLE 16C

    MDR report key: 3820869 · Received May 13, 2014

    Report

    Report Number
    1627487-2014-15361
    Event Type
    Injury
    Date Received
    May 13, 2014
    Date of Event
    April 22, 2014
    Report Date
    April 22, 2014
    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 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 2 OF 2. REFERENCE MFR REPORT: 1627487-2014-15360. IT WAS REPORTED, THE PATIENT EXPERIENCES DISCOMFORT AT THE IPG SITE WHEN HE SITS AND IS NOT RECEIVING THE LEVEL OF RELIEF HE NEEDS FROM THE STIMULATION. SURGICAL INTERVENTION WAS UNDERTAKEN ON (B)(6) 2014 AND THE IPG WAS EXPLANTED. THE LEAD REMAINED IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    286621 LAMITRODE TRIPOLE 16C SCS LEAD GZB ST. JUDE MEDICAL - NEUROMODULATION 3214 3499377

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Other