4,343 results
·
77ms
·
Sources: EU EUDAMED, US FDA
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