BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINI IMPLANTABLE PULSE GENERATOR

    MDR report key: 2080397 · Received April 22, 2011

    Report

    Report Number
    1627487-2011-02480
    Event Type
    Injury
    Date Received
    April 22, 2011
    Date of Event
    February 1, 2011
    Report Date
    March 25, 2011
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    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 3. REFERENCE MANUFACTURER REPORTS: 1627487-2011-02481 AND 1627487-2011-02482. THE PATIENT RECEIVED AN SCS SYSTEM, INCLUDING AN IPG, TWO PERCUTANEOUS LEADS (OF THE SAME LOT) AND TWO ANCHORS (OF THE SAME LOT), ON (B)(6) 2010. IT WAS REPORTED THE ENTIRE SYSTEM WAS EXPLANTED AND NOT REPLACED DUE TO GENERALIZED DISCOMFORT. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EON MINI IMPLANTABLE PULSE GENERATOR TOTALLY IMPLANTABLE PULSE GENERATOR LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3083988

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Required Intervention