BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PENTA

    MDR report key: 3949248 · Received June 25, 2014

    Report

    Report Number
    1627487-2014-08080
    Event Type
    Injury
    Date Received
    June 25, 2014
    Date of Event
    June 5, 2014
    Report Date
    June 5, 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

    IT WAS REPORTED THE PT WAS NOT FEELING RELIEF FROM HIS SCS SYSTEM BUT INSTEAD ONLY FEELS AN UNCOMFORTABLE "ZAPPING" SENSATION UP ON THE RIBS. THE PT IS TO FOLLOW UP WITH HIS PHYSICIAN FOR X-RAYS AND EVAL TO DETERMINE THE NEXT STEPS TO ADDRESS THE ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    369650 PENTA SCS LEAD GZB ST. JUDE MEDICAL ¿ NEUROMODULATION 3228 3872102

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Other IMPLANT DATE| SCS EXTENSION, MODEL 3383 (X2)| SCS IPG, MODEL 3788| IMPLANT DATE