BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CAPSUREFIX NOVUS

    MDR report key: 3861388 · Received June 10, 2014

    Report

    Report Number
    2649622-2014-07299
    Event Type
    Injury
    Date Received
    June 10, 2014
    Date of Event
    April 23, 2014
    Report Date
    April 23, 2014
    Manufacturer
    MPRI
    Product Code
    DTB
    PMA / PMN Number
    P930039
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. CONCOMITANT PRODUCT: 407458 LEAD, IMPLANTED: (B)(6) 2014. (B)(4).

    Description of Event or Problem · 1

    FURTHER INFORMATION WAS OBTAINED INDICATING THAT A DISLODGEMENT WAS CONFIRMED AND THE LEAD WAS REPOSITIONED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT, ONE DAY POST IMPLANT, THE RIGHT ATRIAL (RA) LEAD WAS NOT CAPTURING AND THE SENSING WAS DIMINISHED. A CHEST X-RAY WAS PERFORMED AND THE LEAD APPEARED TO HAVE DROPPED. THE LEAD REMAINS IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    337971 CAPSUREFIX NOVUS ELECTRODE, PACEMAKER, PERMANENT DTB MPRI 407652

    Patients

    Seq Age Sex Outcome Treatment
    1 00070 YR Hospitalization| R ADDR01 IPG