BEUDAMED
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    NEFF INFRARENAL AORTOILIAC CATHETER

    FDA Adverse Event
    Injury ·COOK INCORPORATED·Product code LFK·September 9, 1996

    QUINTON CATHETER

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO·Product code LFK·May 17, 2000

    MEDCOMP PD CATH

    FDA Adverse Event
    Malfunction ·MPS MEDICAL PRODUCT SERVICE GMBH·Product code LFK·May 14, 2007

    ICY FEMORAL CATHETER 3893

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code LFK·January 25, 2013

    UNIVERSAL CAVH CATHETER

    FDA Adverse Event
    Injury ·MEDCOMP·Product code LFK·April 29, 1999

    CARDIOVASCULAR CATHETER

    FDA Adverse Event
    Death ·CR BARD, INC.·Product code LFK·June 23, 1992

    FEMORAL CATHETER

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code LFK·March 7, 2003

    CATHETER

    FDA Adverse Event
    Injury ·VAS-CATH OF CANADA, LTD.·Product code LFK·March 14, 1995

    VOLUMEVIEW FEMORAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code LFK·July 7, 2023

    QUINTON PERMCATH INSERTION KIT

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO·Product code LFK·July 23, 1997

    HOWES LARGE BORE MULTI-LUMEN CENTRAL VEIN CATHETERIZATION KT

    FDA Adverse Event
    ARROW INTERNATIONAL, INC.·Product code LFK·November 7, 1994

    CATHETER, FEMORAL

    FDA Adverse Event
    Injury ·Product code LFK·July 21, 2020

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    FDA Adverse Event
    Death ·ARROW INTL., INC.·Product code LFK·May 14, 1997

    FEM-FLEX FEMORAL CANNULA

    FDA Adverse Event
    Malfunction ·RESEARCH MEDICAL, INC.·Product code LFK·May 12, 1997

    QUINTON

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO·Product code LFK·June 17, 1997

    THIRD PARTY CONMED VCARE

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code LFK·August 12, 2023

    12 FR 3 LUMEN 16 CM CATHETER

    FDA Adverse Event
    Injury ·ARROW·Product code LFK·May 5, 1995

    FEMORAL CATHETER

    FDA Adverse Event
    Injury ·MEDCOMP MEDICAL COMPONENTS, INC.·Product code LFK·November 9, 2001

    FEMORAL CATHETER

    FDA Adverse Event
    Injury ·MEDCOMP MEDICAL COMPONENTS, INC.·Product code LFK·November 9, 2001

    HEMOTECH MCFK60

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code LFK·February 28, 1997