BEUDAMED
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    POWERFLEX P3 BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·November 30, 2006

    PALMAZ MEDIUM ON POWERFLEX PLUS

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·December 11, 2007

    SLALOM THRILL PTA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·March 26, 2007

    POWERFLEX P3 PTA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·February 26, 2007

    PALMAZ GENESIS OPTA PRO

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·April 23, 2008

    PALMAZ GENESIS AMIIA

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·July 10, 2008

    PALMAZ GENESIS 5 X 12, 80CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·March 7, 2008

    PALMAZ GENESIS OPTA PRO

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·March 18, 2008

    SLALOM THRILL PTA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·March 6, 2007

    SLALOM PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·March 29, 2007

    AMIIA PTA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·October 18, 2007

    POWERFLEX P3 PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·December 14, 2007

    POWERFLEX P3 PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·April 30, 2009

    POWERFLEX P3

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·March 27, 2007

    PALMAZ SCHATZ STENT LONG MED 78MMX8

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·February 26, 2007

    PALMAZ GENESIS 6 X 12, 135CM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·January 5, 2007

    PALMAZ MEDIUM ON POWERFLEX PLUS

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·June 9, 2008

    SLALOM THRILL PTA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LTI·January 25, 2007

    PALMAZ MEDIUM ON POWERFLEX PLUS

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·November 7, 2007

    AVIATOR PLUS PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·February 11, 2008