BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EONC

    MDR report key: 2820141 · Received November 2, 2012

    Report

    Report Number
    1627487-2012-01985
    Event Type
    Injury
    Date Received
    November 2, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFORMATION 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 2. REFERENCE MFR REPORT: 1627487-2012-01984. IT WAS REPORTED THE PT IS EXPERIENCING AN UNCOMFORTABLE "PULLING' SENSATION AT HER LEAD SITE AND TENDERNESS AT THE IPG SITE. X-RAYS HAVE BEEN ORDERED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EONC SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3688 3613593

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Required Intervention