BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 2881011 · Received December 14, 2012

    Report

    Report Number
    1627487-2012-13233
    Event Type
    Injury
    Date Received
    December 14, 2012
    Date of Event
    November 20, 2012
    Report Date
    November 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
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IPG WAS INCLUDED IN A 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 2 OF 2. REFERENCE MFR REPORT: 1627487-2012-13232. IT WAS REPORTED THE PT EXPERIENCED HEATING AT THE IPG SITE WHILE RECHARGING HER SCS SYSTEM. THE PT WAS ADVISED TO CHARGE MORE FREQUENTLY FOR LESS TIME. SHE ALSO REPORTED OBSERVING A "CALL SJM" INDICATOR LIGHT ON HER CHARGER. F/U STATED THE PT'S CHARGER IS STILL GETTING VERY WARM EVEN THOUGH SHE HAD REDUCED THE CHARGING TIME. ADD'L F/U IS PENDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EON MINI SCS IPG LGW ST. JUDE MEDICAL, NEUROMODULATION 3788 3798923

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention IMPLANT DATE:| SCS ANCHOR: MODEL 1192| SCS LEAD: MODEL 3219| IMPLANT DATE: