FDANovember 13, 2018device
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
During a post approval study the firm found there was an increased risk of corneal haze following the implantation of this device.
What to do
FDA enforcement status: Terminated
Brands named
rvo 2 0rvo
Recall history
No related federal recalls on record for this brand yet.
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