BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI

    MDR report key: 3123520 · Received May 17, 2013

    Report

    Report Number
    1627487-2013-15659
    Event Type
    Injury
    Date Received
    May 17, 2013
    Date of Event
    November 24, 2012
    Report Date
    April 24, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-07262012-001-C 1
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY AND A FIELD ADVISORY AND 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 3. REFERENCE MFR REPORT: 1627487-2013-15658, REFERENCE MFR REPORT: 1627487-2013-15660.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    219644 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3365316

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Required Intervention SCS ANCHOR: MODEL 1192 (2)| IMPLANT:| IMPLANT:| SCS EXTENSION: MODEL 3341