BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SPRINT QUATTRO SECURE

    MDR report key: 2203495 · Received August 11, 2011

    Report

    Report Number
    2649622-2011-12349
    Event Type
    Malfunction
    Date Received
    August 11, 2011
    Date of Event
    April 13, 2011
    Manufacturer
    MEDTRONIC PUERTO RICO, INC.
    Product Code
    LWS
    PMA / PMN Number
    P920015/S24
    Removal / Correction Number
    Z-0475-2011
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS EVENT OCCURRED OUTSIDE THE U.S. 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 FULL LEAD WAS RETURNED AND ANALYZED. THE DISTAL CONDUCTOR WAS FOUND TO BE DISTORTED. THE INNER TUBING APPEARED KINKED/BUCKLED, AND THE LEAD APPEARED TO HAVE BEEN DAMAGED AT IMPLANT. THE HELIX COULD NOT EXTEND OR RETRACT DUE TO DISTAL CONDUCTOR DISTORTION WITHIN THE CONNECTOR.

    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 FULL LEAD WAS RETURNED AND ANALYZED. THE DISTAL CONDUCTOR WAS FOUND TO BE FRACTURED. THE INNER TUBING APPEARED KINKED/BUCKLED, AND THE LEAD APPEARED TO HAVE BEEN DAMAGED AT IMPLANT. THE HELIX COULD NOT EXTEND OR RETRACT DUE TO DISTAL CONDUCTOR DISTORTION WITHIN THE CONNECTOR.

    Description of Event or Problem · 1

    ASKU

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PHYSICIAN ATTEMPTED TO IMPLANT THE LEAD MULTIPLE TIMES IN THE RIGHT VENTRICLE, BUT THE HELIX WAS NOT WORKING PROPERLY. THE LEAD WAS NOT USED, AND A NEW LEAD WAS IMPLANTED. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SPRINT QUATTRO SECURE IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6947 ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Other