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Bausch & Lomb Surgical, Inc. recalls enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary
Recalled July 22, 2020 · FDA recall Z-2552-2020 · Bausch & Lomb Surgical
Hazard
The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens. · FDA Class II
Units
5
Sold at
U.S. Nationwide distribution including in the states of IN, SC, CT, NV, and NC.
Description
The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens.
Product
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.
Manufacturer(s)
Bausch & Lomb Surgical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →