BEUDAMED
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    ABBOTT MEDICAL OPTICS INC. CARTRIDGE

    FDA Adverse Event
    Injury ·ABBOTT·Product code KYB·September 7, 2017

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·November 6, 2012

    CEEON

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·March 14, 2016

    PHACO MACHINE WHITESTAR SIGNATURE SYSTEM

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code HQC·December 3, 2021

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·March 11, 2016

    Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitrectomy procedure. It is used to remove vitreous from the eye. It has been designed as a disposable (single use)

    FDA Recall
    Terminated ·Johnson & Johnson Surgical Vision Inc·Product code MLZ·September 24, 2018

    Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitrectomy procedure. It is used to remove vitreous from the eye. It has been designed as a disposable (single use)

    FDA Enforcement
    Class II ·Terminated·Johnson & Johnson Surgical Vision Inc·July 10, 2019

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·December 5, 2012

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·November 6, 2012

    Sensar Foldable IOL with OptiEdge. Model number AR40e 21.5 Diopter. The Sensar Foldable IOLs with OptiEdge Design are ultraviolet-absorbing posterior chamber intraocular lenses and are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens are intended to be placed in a capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc (AMO)·Product code HQL·September 20, 2011

    Sensar Foldable IOL with OptiEdge. Model number AR40e, 6.0 Diopter. The Sensar Foldable IOLs with OptiEdge Design are ultraviolet-absorbing posterior chamber intraocular lenses and are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens are intended to be placed in a capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc (AMO)·Product code HQL·September 20, 2011

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·October 17, 2012

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·October 17, 2012

    SENSAR Foldable IOL with OptiEdge Design, Model No. AR40e The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    TECNIS OptiBlue 1-Piece Intraocular Lens (IOL), Model No. ZCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    TECNIS 1-Piece IOL, Model No. ZCB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    SENSAR 1-Piece IOL, Model No. AAB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    TECNIS OptiBlue 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016

    AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model No. Z9002 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.

    FDA Recall
    Terminated ·Abbott Medical Optics Inc. (AMO)·Product code HQL·August 26, 2016