BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IDENTITY ADX XL

    MDR report key: 4191851 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-04136
    Event Type
    Injury
    Date Received
    January 13, 2014
    Date of Event
    September 20, 2012
    Manufacturer
    ST. JUDE MEDICAL, CRMD
    Product Code
    LWP
    PMA / PMN Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFO WAS PROVIDED BY MFR, 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 TO THE REPORTING CRITERIA GOING FORWARD. EVAL DESCRIPTION: ANALYSIS WAS NORMAL. NO ANOMALY WAS FOUND.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHEN THE LEAD WAS CONNECTED TO PULSE GENERATOR THERE WAS AN INCREASE IN THRESHOLD AND A DECREASE IN IMPEDANCE. THE DEVICE WAS PLACED OVER THE PT AND NO CAPTURE WAS NOTED, THE DEVICE WAS EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    29610 IDENTITY ADX XL IMPLANTABLE PACEMAKER PULSE GENERATOR LWP ST. JUDE MEDICAL, CRMD 5286

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention