BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3052838 · Received April 2, 2013

    Report

    Report Number
    1627487-2013-12427
    Event Type
    Injury
    Date Received
    April 2, 2013
    Date of Event
    June 20, 2012
    Report Date
    March 8, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-07262012-001-C
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IPG MODEL NUMBER WAS INCLUDED IN A FIELD CORRECTION. 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 1 OF 2. REF MFR REPORT #1627487-2013-12428. IT WAS REPORTED THE PT EXPERIENCES HEATING AT THE IPG POCKET SITE WHILE CHARGING SINCE THE IMPLANT DATE. PT ALSO REPORTED DISCOMFORT AT THE IPG POCKET SITE UNRELATED TO CHARGING. PT HAS BEEN UNABLE TO GET TO THE PHYSICIAN'S OFFICE TO RECEIVE A NEW CHARGER. ON (B)(4) 2012. ST. JUDE MEDICAL, NEUROMODULATION DIVISION, 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
    135373 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3710514

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Required Intervention IMPLANT DATE:| SCS LEAD, MODEL 3586| IMPLANT DATE:| SCS LEAD, MODEL 3186