Alcon Research, Ltd.: Medical Device Recalls in 2017

According to to data from the FDA, there were 5 medical device recalls made by Alcon Research, Ltd. in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery
• Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal
• ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
• Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical professionals for specific procedures. The Patient Care kits are configured with customer-specific components
• LX3 Floor Stand for LuxOR Ophthalmic Microscope; Endure LuxOR Q-VUE Ophthalmic Microscope. LX3 Microscope Floor Stands are not stand-alone medical devices, but are used in combination with the LuxOR Ophthalmic Microscope and the LuxOR Ophthalmic Microscope with Q-VUE 3-D Assistant Visualization. These microscopes are used for low magnification visualization during cataract, retina, and cornea surgeries