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AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Recalled August 27, 2014 · FDA recall Z-2274-2014 · AMO Puerto Rico Manufacturing
Hazard
Units may be labeled with the incorrect diopter power. · FDA Class II
Units
77,055 IOLs in total
Sold at
Worldwide Distribution - Nationwide (USA and Puerto Rico), and foreign: Latin America, Asia Pacific, Canada, Europe, Africa and Middle East, and Japan.
Description
Units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 12.0 and 12.5 Product Usage: AMO TECNIS CL monofocal foldable IOLs with OptiEdge design are ultraviolet-absorbing posterior chamber intraocular lenses which compensate for corneal spherical aberrations. TECNIS CL Silicone Intraocular Lenses are indicated for primary implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction or phacoemulsification. These devices are intended to be placed in the capsular bag.
Manufacturer(s)
AMO Puerto Rico Manufacturing, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →