BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EON MINI

    MDR report key: 3182381 · Received June 14, 2013

    Report

    Report Number
    1627487-2013-13917
    Event Type
    Malfunction
    Date Received
    June 14, 2013
    Date of Event
    April 20, 2013
    Report Date
    May 20, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-12192011-003-R
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY. 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 PATIENT COULD NOT COMMUNICATE WITH HIS IPG USING EXTERNAL DEVICES. A SJM REPRESENTATIVE MET WITH THE PATIENT AND CONFIRMED THE EVENT. THE PATIENT STATED HE HAS NOT CHARGED HIS IPG FOR THE LAST THREE MONTHS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271363 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3213640

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR SCS ANCHOR: MODEL 1192 (2)| IMPLANT:| IMPLANT:| SCS LEAD: MODEL 3186 (2)