BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIA VDD

    MDR report key: 2123198 · Received June 14, 2011

    Report

    Report Number
    6000094-2011-00713
    Event Type
    Injury
    Date Received
    June 14, 2011
    Date of Event
    February 18, 2011
    Manufacturer
    MEDTRONIC S.A.
    Product Code
    NVZ
    PMA / PMN Number
    P980035/S097
    Removal / Correction Number
    ASKU
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PL
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. EVALUATION SUMMARY (B)(4) THE DEVICE WAS RETURNED AND ANALYZED. NO ANOMALIES WERE FOUND.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING FOLLOW-UP THE DAY AFTER IMPLANT THERE WAS ATRIAL UNDERSENSING. WHEN THE IMPLANTABLE PULSE GENERATOR (IPG) AND LEAD REVISION WAS SCHEDULED THERE WAS BLOOD FOUND IN THE CONNECTOR BLOCK OF THE IPG. IT WAS DECIDED TO EXPLANT AND REPLACE THE IPG. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RELIA VDD IMPLANTABLE PULSE GENERATOR NVZ MEDTRONIC S.A. REVDD01 ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R