BEUDAMED
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    INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB INCORPORATED·Product code HQL·June 5, 2025

    MILLENIUM MICROSURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB SURGICAL, INC·Product code HQE·February 9, 2007

    BAUSCH & LOMB, INC.

    FDA Adverse Event
    Injury ·*·Product code LPL·June 3, 2013

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQC·February 7, 2008

    CAPSULORHEXIS FORCEPS AND FORCEPS, OPHTHALMIC

    FDA Adverse Event
    Other ·BAUSCH & LOMB·Product code HNR·February 6, 2025

    Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient

    FDA Enforcement
    Class II ·Terminated·Bausch & Lomb, Inc.·January 18, 2017

    BAUSCH AND LOMB PUR VISION LENSES

    FDA Adverse Event
    Other ·BAUSCH & LOMB·Product code LPL·October 25, 2012

    Boston ES Rigid Gas Permeable Contact lens manufactured with Fluoro Silicone Acrylate Rigid Gas Permeable Contact Lens Material. Bausch & Lomb, Inc. Wilmington, MA 01887. Indicated for daily wear for the correction of refractive ametropia in aphakic and/or not-aphakic persons with non-diseased eyes.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQD·April 20, 2010

    Adapt AO, Akreos Advanced Optics Aspheric Lens. Bausch & Lomb Incorporated, Rochester, NY. Manufactured by Bausch & Lomb Incorporated, Clearwater, FL.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQL·December 8, 2008

    Bausch & Lomb Stellaris Basic Vacuum Phaco Pack, Ref: BL5111, packaged 6 units/case, RX, Sterile. Bausch & Lomb Incorporated, Rochester, NY For use with the Bausch & Lomb Stellaris Vision Enhancement System for the phacoemulsification of an opacified crystalline lens during anterior segment surgery

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQC·July 27, 2011

    Bausch & Lomb Stellaris Optimized Stability Vacuum Pack, Ref: BL5112, packaged 6 units/case, RX, Sterile. Bausch & Lomb Incorporated, Rochester, NY For use with the Bausch & Lomb Stellaris Vision Enhancement System for the phacoemulsification of an opacified crystalline lens during anterior segment surgery

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQC·July 27, 2011

    Bausch & Lomb Stellaris Premium Vacuum Phaco Pack, Ref: BL5110, packaged 6 units/case, RX, Sterile. Bausch & Lomb Incorporated, Rochester, NY For use with the Bausch & Lomb Stellaris Vision Enhancement System for the phacoemulsification of an opacified crystalline lens during anterior segment surgery.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQC·July 27, 2011

    Bausch & Lomb Stellaris 1.8mm Premium Vacuum Phaco Pack with MICS Needle, Ref: BL5114, packaged 6 units/case, RX, Sterile. Bausch & Lomb Incorporated, Rochester, NY For use with the Bausch & Lomb Stellaris Vision Enhancement System for the phacoemulsification of an opacified crystalline lens during anterior segment surgery

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQC·July 27, 2011

    Bausch & Lomb SoFlex SE Foldable Intraocular Lens. UPC 4001404, Rx Only, STERILE. Manufactured by: Bausch & Lomb Incorporated, 21 Park Place Boulevard, Clearwater, FL 33759. Intraocular lens indicated for primary implantation for visual correction in adult patients where the cataractous lens has been removed by phacoemulsification. The lens is intended for placement in the capsular bag.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code HQL·November 19, 2009

    CRYSTALENS

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code NAA·February 25, 2011

    ACUVUE CONTACT LENSES-SPECIFIC BRAND UNKNOWN

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 8, 2010

    Amvisc Sodium Hyaluronate 0.8 mL. Bausch & Lomb, Inc., Rochester, NY Product Numbr: 59081

    FDA Recall
    Terminated ·Anika Therapeutics, Inc.·Product code LZP·July 14, 2005

    Amvisc Sodium Hyaluronate 0.5 mL. Bausch & Lomb, Inc., Rochester, NY Product Number: 59051

    FDA Recall
    Terminated ·Anika Therapeutics, Inc.·Product code LZP·July 14, 2005

    Amvisc Plus Sodium Hyaluronate 0.8 mL. Bausch & Lomb, Inc., Rochester, NY Product Number: 60081

    FDA Recall
    Terminated ·Anika Therapeutics, Inc.·Product code LZP·July 14, 2005

    Amvisc Plus Sodium Hyaluronate 0.5 mL. Bausch & Lomb, Inc., Rochester, NY Product Number: 60051

    FDA Recall
    Terminated ·Anika Therapeutics, Inc.·Product code LZP·July 14, 2005