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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall AcrySof ReSTOR Intraocular Lens Ophthalmic Devices Alcon Laboratories, Inc 3 United States USFDA
Device Recall AcrySof ReSTOR Intraocular Lens Ophthalmic Devices Alcon Laboratories, Inc 3 United States USFDA
Device Recall ACUVUE ADVANCE Brand Contact Lens Ophthalmic Devices Johnson & Johnson Vision Care, Inc. 2 United States USFDA
Device Recall ACUVUE OASYS BRAND CONTACT LENSES for ASTIGMATISM with HYDRACLEAR Plus (senofilcon A) Ophthalmic Devices Vistakon 3 United States USFDA
Device Recall Alcon Ophthalmic Devices Ellex Medical Pty Ltd 2 United States USFDA
Device Recall Alcon 23G NonValved Trocar Cannula and Infusion Cannula Ophthalmic Devices Alcon Research, LTD. 1 United States USFDA
Device Recall Alcon 25 TOT ALPLUS Vitrectomv Pak Ophthalmic Devices Alcon Research, LTD. 2 United States USFDA
Device Recall Alcon Accurus Standalone Vitreous Probe Paks Ophthalmic Devices Alcon Research, Ltd. 2 United States USFDA
Device Recall Alcon/Grieshaber Morris ILM Forceps, Direct Action Ophthalmic Devices Alcon Research, Ltd 1 United States USFDA
Device Recall Alcon Ladarwave Ophthalmic Devices Alcon Laboratories, Inc. United States USFDA
Device Recall Alcon Trocar Cannula Replacement Plug Ophthalmic Devices Alcon Research, Ltd 1 United States USFDA
Device Recall Alden Classic 38 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden Classic 55 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP49 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP49 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP54 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP54 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP59 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP59 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall AMO brand WaveScan WaveFront System Ophthalmic Devices AMO Manufacturing USA, LLC 3 United States USFDA
Device Recall AMO Prestige Pack Ophthalmic Devices Allergan Medical Optics Inc 2 United States USFDA
Device Recall AMO VISX STAR Excimer Laser System Ophthalmic Devices VISX INCORPORATED, A SUBSIDIARY OF AMO INC 3 United States USFDA
Device Recall AMO Vitrectomy Cutter Ophthalmic Devices Abbott Medical Optics Inc. (AMO) 2 United States USFDA
Device Recall AMO WaveScan WaveFront System v3.65 Ophthalmic Devices VISX INCORPORATED, A SUBSIDIARY OF AMO INC 3 United States USFDA
Device Recall AMO WaveScan WaveFront System Version 3.90/3.901 Ophthalmic Devices VISX INCORPORATED, A SUBSIDIARY OF AMO INC 3 United States USFDA