|Articles|August 4, 2004
FDA recalls one lot of Carl Zeiss Meditec medical device
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.
Advertisement
Newsletter
Don’t miss out—get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.
Advertisement
Latest CME
Advertisement
Advertisement
Trending on Ophthalmology Times - Clinical Insights for Eye Specialists
1
Metformin use associated with reduced incidence of intermediate AMD
2
Ocumetics reports first-in-human data investigational accommodating IOL in severe vision loss
3
EnVision Summit 2026: Ultimate gathering place for ophthalmic education
4
Sandoz Canada launches aflibercept biosimilar, Enzeevum
5
























