Bausch & Lomb Surgical, Inc.: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Bausch & Lomb Surgical, Inc. in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary implantation in the capsular bag of the eye in adult patients for visual correction of aphakia and corneal astigmatism following removal of a cataractous lens for improved uncorrected distance vision.
MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is intended for placement in the capsular bag.