BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PY2 PACING LEAD

    MDR report key: 3841146 · Received February 26, 2014

    Report

    Report Number
    1035166-2014-00008
    Event Type
    Malfunction
    Date Received
    February 26, 2014
    Date of Event
    November 1, 2013
    Report Date
    February 25, 2014
    Manufacturer
    OSCOR INC.
    Product Code
    DTB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE LEAD WAS CAPPED, THEREFORE IT WILL NOT BE RETURNED FOR ANALYSIS. AS A RESULT, THE ALLEGATIONS AGAINST THIS LEAD CANNOT BE CONFIRMED. NO SUBSEQUENT DEVICE OR CLINICAL ADVERSE EVENTS HAVE BEEN REPORTED. THE EVENT WILL BE RE-EVALUATED IF ADD'L INFO BECOMES AVAILABLE. THE DEVICE HISTORY RECORDS AND THE COMPLAINT FILES OF THE LEAD MODEL WERE REVIEWED. NO TREND OF THE SAME OR SIMILAR TYPE WAS FOUND OR INDICATED.

    Description of Event or Problem · 1

    ON (B)(6) 2014, THE CUSTOMER REPORTED ACCORDING TO THE SALES REPRESENTATIVE THIS LEAD WAS CAPPED ON (B)(6) 2013 DUE TO FAILURE TO CAPTURE. THERE WERE NO OTHER ADVERSE PATIENT EVENTS REPORTED. HE LEAD WAS ACTIVELY IMPLANTED FOR APPROXIMATELY 6 YEARS, 7 MONTHS. UPDATED INFO REC'D FROM THE CUSTOMER ON (B)(6) 2014 THE CUSTOMER REPORTED ACCORDING TO THE SALES REPRESENTATIVE THIS LEAD WAS CAPPED ON (B)(6) 2013 DUE TO FAILURE TO CAPTURE. NO SUBSEQUENT DEVICE OR CLINICAL ADVERSE EVENTS HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    118763 PY2 PACING LEAD RETRACTABLE SCREW-IN PACING LEAD DTB OSCOR INC. ELAFIX P2P 752 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR