Recall of the intraocular lens model EC-3 from Ophthalmic Innovations International
2006.09.29
Product group Non-active implants
Reference 02503/06
Ophthalmic Innovations International, Inc. (OII) is conducting a voluntary recall of the intraocular lens model EC-3 because of detected small amounts of water soluble wax on the surface of the lens which was used in the manufacturing process.There have been no reports of any adverse events of implanted patients.