FDANovember 5, 2018device

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual correction of aphakia in adult patients in whom the cataractous lens has been removed. The lens is intended for placement in the capsular bag.

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

The hazard

Cosmetic imperfections on the surface of some lenses.

What to do

FDA enforcement status: Terminated

Brands named

bausch lomb surgicalbauschbausch lomb

Recall history

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

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