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    Filters Status: Malfunction ×

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·May 1, 2009

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·May 1, 2009

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·May 7, 2009

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·August 12, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·December 10, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·January 25, 2016

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·March 4, 2016

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·February 19, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·February 11, 2015

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·February 20, 2015

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIP·April 1, 2015

    COMPLETE SE SFA-IDE

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·March 11, 2009

    COMPLETE SE SFA - IDE

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIO·June 13, 2012

    COMPLETE SE SFA - IDE

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIO·June 13, 2012

    COMPLETE SE SFA - IDE

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIO·June 13, 2012

    COMPLETE SE SFA STENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·July 15, 2009

    A SPIRE

    FDA Adverse Event
    Malfunction ·VASCULAR ARCHITECTS, INC.·Product code JCT·February 13, 2004

    CONFIANZA PRO 12

    FDA Adverse Event
    Malfunction ·ASAHI INTECC·Product code DQX·August 3, 2022

    ASPIRE

    FDA Adverse Event
    Malfunction ·VASCULAR ARCHITECTS·Product code NIP·June 12, 2003

    SMART 120 150, SFA - 6X150MM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code FGE·November 8, 2017