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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Sterile BioEye Hydroxyapatite Orbital Implant and Conformer Ophthalmic Devices Integrated Orbital Implants Inc 2 United States USFDA
Device Recall Molteno3 Glaucoma Implants GSeries Ophthalmic Devices Innovative Ophthalmic Products, Inc 2 United States USFDA
Device Recall Venus Eye Sphere 10 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 12 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 14 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 16 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 18 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 20 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Venus Eye Sphere 22 mm (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Small (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Medium (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Large (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Small with holes (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Medium with holes (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall Conformer Medium with holes (sterile) Ophthalmic Devices Gulden Ophthalmics 2 United States USFDA
Device Recall MEDPOR Surgical Implant, Catalog 6317, 20mm Sphere Ophthalmic Devices Porex Surgical, Inc. 2 United States USFDA
Device Recall BioEye Ophthalmic Devices Integrated Orbital Implants Inc 2 United States USFDA
Device Recall Ocular Motility Peg system Ophthalmic Devices Integrated Orbital Implants Inc 2 United States USFDA
Krupin Eye Valve Ophthalmic Devices Eagle Vision Inc 2 United States USFDA
Glaucoma Aqueous Shunt, 209 mm, valved Ophthalmic Devices Eagle Vision Inc 2 United States USFDA
Glaucoma Aqueous Shunt 365 mm, valved Ophthalmic Devices Eagle Vision Inc 2 United States USFDA
ValveEV Glaucoma UltraSmooth Ophthalmic Devices Eagle Vision Inc 2 United States USFDA
Device Recall Coated BioEye Orbital Implant w/Conformer. Ophthalmic Devices Integrated Orbital Implants Inc 2 United States USFDA
Device Recall MEDPOR PLUS Ophthalmic Devices Howmedica Osteonics Corp dba Stryker Craniomaxillofacial 2 United States USFDA
Device Recall Aaren Scientific Intraocular Lens (IOL), Part No. EC3 PAL Ophthalmic Devices Aaren Scientific, Incorporated 3 United States USFDA