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Rayner Intraocular Lenses Limited recalls C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the capsu
Recalled October 10, 2018 · FDA recall Z-3282-2018 · Rayner Intraocular Lenses
Hazard
Firm become aware of reports of post-operative refractive errors following implantation of lenses. · FDA Class II
Units
49
Sold at
US in the states of MO
Description
Firm become aware of reports of post-operative refractive errors following implantation of lenses.
Product
C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the capsular bag of the human eye as a replacement for the crystalline lens following phacoemulsification
Manufacturer(s)
Rayner Intraocular Lenses Limited
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →