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    Filters Status: Malfunction ×

    CARDICA, INC PASPORT PROXIMAL ANASTAMOSIS SYSTEM

    FDA Adverse Event
    Malfunction ·CARDICA, INC·Product code FZP·August 8, 2016

    C-PORT XA DISTAL ANASTOMOSIS SYSTEM

    FDA Adverse Event
    Malfunction ·CARDICA, INC.·Product code FZP·June 30, 2010

    PAS-PORT

    FDA Adverse Event
    Malfunction ·CARDICA, INC.·Product code FZP·August 21, 2015

    PAS-PORT

    FDA Adverse Event
    Malfunction ·CARDICA, INC·Product code FZP·April 21, 2009

    PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM

    FDA Adverse Event
    Malfunction ·CARDICA, INC.·Product code FZP·September 9, 2011

    C-PORT XA DISTAL ANASTOMOSIS SYSTEM

    FDA Adverse Event
    Malfunction ·CARDICA, INC.·Product code FZP·January 29, 2009

    CARDIAC PACEMAKERS, INC

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC.·Product code LWS·September 16, 1997

    CARDIAC PACEMAKERS, INC.

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC.·Product code DXY·December 5, 1994

    CARDIAC PACEMAKER, INC.

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC.·Product code DXY·November 18, 1996

    CARDIAC PACEMAKERS, INC

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC./ELI LILLY AND CO.·Product code DXY·March 9, 1998

    PATHFINDER 20, 2-6-2, 135

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DRF·January 29, 2004

    VUEPORT, AMPLATZ, 90CM

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DQY·November 25, 2003

    PATHFINDER 020, 6, 2-5-2, 135

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DRF·December 16, 2003

    PATHFINDER 16, 2-6-2, 135

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DRF·November 25, 2003

    *

    FDA Adverse Event
    Malfunction ·CARDIMA, INC·Product code DQO·July 26, 2003

    PATHFINDER

    FDA Adverse Event
    Malfunction ·CARDIMA INC.·Product code DRF·November 22, 2008

    PATHFINDER 16

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DRF·May 15, 2009

    VENAPORT, MP, 90

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DQY·July 31, 2002

    VENAPORT

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DQY·November 26, 2001

    VENAPORT,MP,90

    FDA Adverse Event
    Malfunction ·CARDIMA, INC.·Product code DQY·December 18, 2001