BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3141457 · Received May 24, 2013

    Report

    Report Number
    1627487-2013-13807
    Event Type
    Injury
    Date Received
    May 24, 2013
    Date of Event
    May 11, 2012
    Report Date
    May 6, 2013
    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
    IA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    RECALL NUMBERS - 1627487-12192011-003-R AND 1627487-07262012-002-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: 1627487-2013-13808. THE PT REPORTED SHE HAD EXPERIENCED A BURN WHILE RECHARGING HER IPG ON (B)(6) 2012. THE PT STATED SHE STOPPED CHARGING AND USING HER SCS SYSTEM SINCE RECEIVING THE BURN. THE BURN WAS TREATED BY THE PT'S PHYSICIAN. A NEW CHARGER WAS SENT TO THE PT. 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
    231688 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3677 2834054

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention IMPLANTED:| SCS LEAD: MODEL 3219