martes, 5 de marzo de 2019

Medical Device Recalls > RVO 2.0, Inc. Recalls Raindrop Near Vision Inlay Due to Risk of Increased Risk of Corneal Haze

Medical Device Recalls > RVO 2.0, Inc. Recalls Raindrop Near Vision Inlay Due to Risk of Increased Risk of Corneal Haze

U.S. Food and Drug Administration

RVO 2.0, Inc. Recalls Raindrop Near Vision Inlay Due to Risk of Increased Risk of Corneal Haze
RVO 2.0 is recalling the Raindrop Near Vision Inlay because data from the post-approval study showed an increased risk of corneal haze (a type of cloudiness in the cornea due to inflammation) associated with the device. The device is now owned by RVO 2.0, doing business as Optics Medical.

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