Safety Communications > Increased Risk of Corneal Haze Associated with the Raindrop Near Vision Inlay: FDA Safety Communication

Safety Communications > Increased Risk of Corneal Haze Associated with the Raindrop Near Vision Inlay: FDA Safety Communication

Increased Risk of Corneal Haze Associated with the Raindrop Near Vision Inlay: FDA Safety Communication

This notice is to alert eye care providers and patients already implanted with the Raindrop Near Vision Inlay of the increased risk of corneal haze (a type of cloudiness in the cornea due to inflammation) associated with the device. The FDA is advising that eye care providers not implant Raindrop inlays and is working with Optics Medical to have all remaining product on the market recalled. Raindrop Inlays are no longer being distributed in the U.S. Continue reading.