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    ALCON LABORATORIES

    FDA Adverse Event
    Injury ·ALCON LABORATORIES·Product code HQC·October 29, 2003

    ALCON LABORATORIES

    FDA Adverse Event
    Injury ·ALCON MANUFACTURING, LTD.·Product code HQC·December 16, 2005

    ALCON LABORATORIES

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code MFK·May 22, 2008

    ALCON LABORATORIES

    FDA Adverse Event
    Malfunction ·ALCON LABS INC.·Product code HQL·July 9, 2010

    ALCON LABORATORIES, INC.

    FDA Adverse Event
    Malfunction ·ALCON·Product code HQL·March 26, 2012

    ALCON LABORATORIES, INC.

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·August 25, 2000

    ALCON LABORATORIES, INC.

    FDA Adverse Event
    Injury ·*·Product code HQL·August 23, 2004

    ALCON LABORATORIES, INC.

    FDA Adverse Event
    Injury ·Product code HQL·November 8, 2007

    ALCON LABORATORIES, INC

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES·Product code HQL·June 17, 2004

    ALCON LABORATORIES INC, ACRYSOFIQ

    FDA Adverse Event
    Injury ·ALCON LAB, INC·Product code HQL·March 16, 2009

    DUOVISC

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES INC.·Product code LZP·December 8, 2017

    PROVISC

    FDA Adverse Event
    Injury ·ALCON LABORATORIES·Product code LZP·May 19, 2004

    ALCON INJECTOR MONARCH III D CARTRIDGE

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES·Product code KYB·December 22, 2009

    ALCON ACRYSOF IOL IMPLANT

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code HQL·March 14, 2001

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES·Product code HQE·August 12, 1997

    *

    FDA Adverse Event
    Malfunction ·ALCON LABS·Product code HOY·March 18, 2002

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·December 22, 1997

    CONSTELLATION

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD.·Product code HQC·April 12, 2013

    ALCON EYE SPEARS-CELLULOSE SPONGES- 10/PK

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code HOZ·September 15, 2009

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·October 16, 1997