BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RIATA ST ACTIVE FIXATION LEAD

    MDR report key: 3890377 · Received January 13, 2014

    Report

    Report Number
    2938836-2014-03613
    Event Type
    Injury
    Date Received
    January 13, 2014
    Date of Event
    November 20, 2012
    Manufacturer
    ST. JUDE MEDICAL INC., CRMD
    Product Code
    LWS
    PMA / PMN Number
    P950022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. THIS HISTORICAL COMPLAINT IS BEING FILED AS PART OF A RETROSPECTIVE REVIEW OF COMPLAINT FILES IN RESPONSE TO A RECENT FDA INSPECTION. THERE IS NO CHANGE TO THE ACTUAL PERFORMANCE OF THE PRODUCT AND THIS REPORT ONLY REPRESENTS AN ENHANCEMENT OT THE REPORTING CRITERIA GOING FORWARD. A PARTIAL MODEL 7000 LEAD WAS RETURNED CUT IN TWO SEGMENTS FOR ANALYSIS. THE CONNECTOR PORTION MEASURE 13.4CM AND THE DISTAL PORTION MEASURE 46.8CM. APPROXIMATELY 4.8CM OF INSULATION FROM THE DISTAL PORTION WAS NOT RETURNED. ANALYSIS WAS NORMAL. NO ANOMALY WAS FOUND.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE LEAD WAS REPLACED DUE TO NOISE AND POSSIBLE INAPPROPRIATE THERAPIES DURING INTERROGATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30405 RIATA ST ACTIVE FIXATION LEAD DEFIBRILLATION LEAD LWS ST. JUDE MEDICAL INC., CRMD 7000/65

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Required Intervention