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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall OASIS Medical Vidaurri LASIK Flap Irrigator Ophthalmic Devices Oasis Medical Inc 1 United States USFDA
Device Recall AQuify Ophthalmic Devices Ciba Vision Corporation 2 United States USFDA
Device Recall BD Ophthalmic Ophthalmic Devices BD Opthalmic Systems 1 United States USFDA
Device Recall Circle Lens, Europa, Pacifica, Gothika and Water Color. Ophthalmic Devices Hebron International, Inc. 2 United States USFDA
Device Recall Focus DAILIES Ophthalmic Devices Ciba Vision Corporation 2 United States USFDA
Device Recall OASIS Medical SOFT PLUG Ophthalmic Devices Oasis Medical Inc Unclassified United States USFDA
Device Recall Bausch & Lomb Lightning High Speed Vitrectomy Cutter Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall Bausch & Lomb Millennium 20 Ga. High Speed Posterior Vitrectomy Pack Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
Device Recall AcrySof ReSTOR Intraocular Lens Ophthalmic Devices Alcon Laboratories, Inc 3 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall BD Beaver Ophthalmic Devices Becton Dickinson and Company 1 United States USFDA
Device Recall OOptix (lotrafilcon B) Soft Contact Lenses Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
Device Recall Alcon Trocar Cannula Replacement Plug Ophthalmic Devices Alcon Research, Ltd 1 United States USFDA
Device Recall CustomPak Surgical Packs Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA