FDAJune 9, 2020device

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 uncor...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens.

What to do

FDA enforcement status: Terminated

Brands named

bausch lomb surgicalbauschbausch lomb

UPCs

10757770555199

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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