BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICRONY II SR+

    MDR report key: 4121568 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-07709
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    September 3, 2012
    Manufacturer
    ST. JUDE MEDICAL, INC., CRMD
    Product Code
    LWP
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    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 REPRESENTS AN ENHANCEMENT TO THE REPORTING CRITERIA GOING FORWARD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A DEVICE INTERROGATED NORMALLY THEN DISPLAYED AN ERROR MESSAGE FORCING THE PROGRAMMER TO BE REBOOTED. FOLLOWING THE REBOOT, THE DEVICE COULD NOT BE INTERROGATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    32293 MICRONY II SR+ IMPLANTABLE PACEMAKER PULSE GENERATOR, LWP LWP ST. JUDE MEDICAL, INC., CRMD 2525T

    Patients

    Seq Age Sex Outcome Treatment
    1