BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 2792043 · Received October 12, 2012

    Report

    Report Number
    1627487-2012-02510
    Event Type
    Injury
    Date Received
    October 12, 2012
    Date of Event
    September 20, 2012
    Report Date
    September 20, 2012
    Manufacturer
    ST. JUDE MEDICAL NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-07262012-001-C
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    CORRECTION NUMBERS: 1627487-05242011-002-R AND 1627487-12192011-003-R. THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY AND FIELD CORRECTION. 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

    DEVICE 1 OF 2. REFERENCE MFR REPORT: 1627487-2012-02511. IT WAS REPORTED THE PT FEELS UNCOMFORTABLE HEATING AT THE IPG POCKET AFTER ABOUT 10 MINUTES OF CHARGING. THE PT STATED ADDING EXTRA SPACE HELPS WITH THE HEATING DURING CHARGING BUT IS BOTHERSOME. SHE ALSO REPORTED HER IPG IS MORE SHALLOW AND HER STIMULATION COVERAGE IS APPROPRIATE BUT DOES NOT HELP HER PAIN. IT WAS REPORTED SHE PLANS TO FOLLOW UP WITH HER PHYSICIAN REGARDING THE ISSUES. NO FURTHER INFO IS AVAILABLE AT THIS TIME. ON (B)(6) 2012 ST. JUDE MEDICAL, NEUROMODULATION DIV, SENT FIELD ACTION LETTERS TO PTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PTS. AN INCREASE IN PRIOR NON-REPORTED HEATING WHILE CHARGING EVENTS AND OTHER NON-REPORTED EVENTS WAS EXPECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EON MINI SCS IPG LGW ST. JUDE MEDICAL NEUROMODULATION 3788 176468

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Required Intervention SCS LEAD: MODEL 3219| IMPLANT DATE: