Bausch & Lomb Surgical, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0519-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is intended for placement in the capsular bag.

Product Classification:

Class II

Date Initiated: November 7, 2020

Date Posted: December 9, 2020

Recall Number: Z-0519-2021

Event ID: 86721

Reason for Recall:

Product may be missing toric axis marks.

Status: Terminated

Product Quantity: 31 devices

Code Information:

Lot number: 3043816 Serial numbers: 3043816001 3043816002 3043816003 3043816004 3043816005 3043816006 3043816007 3043816008 3043816009 3043816010 3043816011 3043816012 3043816013 3043816014 3043816015 3043816016 3043816017 3043816018 3043816019 3043816020 3043816023 3043816024 3043816025 3043816026 3043816027 3043816028 3043816029 3043816030 3043816031

Distribution Pattern:

US Nationwide distribution including in the states of FL, CA, MO, MN, TN, TX, MI, WA, UT, NH, and OH.

Voluntary or Mandated:

Voluntary: Firm initiated