Article
Carl Zeiss Meditec, upon notification from the FDA, recalled one lot of its Visulink 532/U surgical laser instruments because of a possible defective mirror coating. No other lots of the Visulink 532/U or any other Carl Zeiss Meditec devices were involved in the action.
Don’t miss out—get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.