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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall FreshLook ColorBlends Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
Device Recall FreshLook Colors Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
Device Recall FreshLook Enhancers Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
Device Recall FreshLook Toric Ophthalmic Devices Ciba Vision Corporation 3 United States USFDA
MicroSTAAR Injector w/ Foam Tip Plunger, Model MSI-PF Ophthalmic Devices Staar Surgical Co Inc 1 United States USFDA
Device Recall AMO Prestige Pack Ophthalmic Devices Allergan Medical Optics Inc 2 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Stylus Brand Angled Knives Ophthalmic Devices Surgical Specialties Puerto Rico, Inc. 1 United States USFDA
Device Recall Private Eyes Ophthalmic Devices The Contact Lens Store, Inc. 2 United States USFDA
Battery-operated Cautery || Low Temperature, fine/elongated Tip Ophthalmic Devices Aaron Medical Industries, Inc. 2 United States USFDA
Battery-operated Cautery || High Temperature, fine/Loop/ Vasectomy Tip Ophthalmic Devices Aaron Medical Industries, Inc. 2 United States USFDA
Device Recall Soft Contact Lens Ophthalmic Devices Ocular Sciences, Inc. 2 United States USFDA
SofLens 66 Toric Visibility Tinted Contact Lenses for Daily Wear, sold in cartons containing 6 lenses each. Cartons/blister packs are labeled with -3.25 DS, || -1.25DC, 170 degree Axis. Firm on label: Manufactured by Bausch & Lomb, Waterford, Ireland. Ophthalmic Devices Bausch & Lomb Inc 2 United States USFDA
CLARIS Cleaning and Soaking Solution, 4 fl. oz. Ophthalmic Devices Advanced Medical Optics, Inc. 2 United States USFDA
Device Recall STAAR Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Device Recall Cytosol Opthalmics Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Device Recall Bausch & Lomb Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Device Recall Bausch & Lomb Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Device Recall Bausch & Lomb Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Device Recall Bausch & Lomb Ophthalmic Devices Anika Therapeutics, Inc. 3 United States USFDA
Staarvisic II || Sodium Hyaluronate, 0.8 mL Ophthalmic Devices Staar Surgical Co Inc 3 United States USFDA