BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FINELINE II

    MDR report key: 1043425 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33226
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 6, 2008
    Report Date
    February 6, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DTB
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FINELINE II IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4473 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR Required Intervention THE DEVICE 1290/805567 WAS IMPLANTED 22-JAN-2008| THE DEVICE 4456/454123 WAS IMPLANTED 07-FEB-2008| THE DEVICE 4472/420556 WAS IMPLANTED 22-JAN-2008| THE DEVICE 4473/452608 WAS IMPLANTED 06-FEB-2008