|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
Iolyx Therapeutics and Laboratoires Théa enter into agreement over ILYX-002 for the treatment of OSD
2
PainReform launches development plan for OcuRing-K, readies phase 2 trial
3
Avisi Technologies treats first patient in SAPPHIRE trial for glaucoma
4
Phase 1 trial findings confirm safety and tolerability of Huons’ dry eye therapy
5











































.png)


