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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall ORA System with VerifEye Ophthalmic Devices Alcon Research, Ltd. 1 United States USFDA
Device Recall Pentacam AXL Ophthalmic Devices Oculus Optikgeraete GMBH 2 United States USFDA
Device Recall Alcon 25 TOT ALPLUS Vitrectomv Pak Ophthalmic Devices Alcon Research, LTD. 2 United States USFDA
Device Recall Custom Pak (Custom Pak in which Alcon 25 TOTALPLUS Vitrectomy Pak is a component.) Ophthalmic Devices Alcon Research, LTD. 2 United States USFDA
Device Recall The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser Ophthalmic Devices SIE AG, Surgical Instrument Engineering 2 United States USFDA
Device Recall NovaKone Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall NovaKone Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden Classic 38 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 HP59 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 Classic 55 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Alden HP59 Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall ASTERA Ophthalmic Devices Alden Optical 2 United States USFDA
Device Recall Widefield OCT software Ophthalmic Devices Heidelberg Engineering 2 United States USFDA
Device Recall AUTO REF/KERATOMETER ARK1s Ophthalmic Devices Nidek Inc. 1 United States USFDA
Device Recall Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) Ophthalmic Devices Reliance Medical Products Inc 1 United States USFDA
Device Recall clariti 1 day/Fresh Day 90 pack Ophthalmic Devices CooperVision Inc. 2 United States USFDA
Device Recall clariti 1 day (1.25) 90 pack Ophthalmic Devices CooperVision Inc. 2 United States USFDA
Device Recall 56 1 Day Silicone Hydrogel (10 pack) Ophthalmic Devices CooperVision Inc. 2 United States USFDA
Device Recall 56 1 Day Silicone Hydrogel (10 pack) Ophthalmic Devices CooperVision Inc. 2 United States USFDA
Device Recall HYPA C7 Ophthalmic Devices My Cosmetics Inc 2 United States USFDA
Device Recall SKBM Microkeratome Ophthalmic Devices Alcon Laboratories, Inc 1 United States USFDA