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Alden Optical recalls NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated fo
Recalled March 21, 2018 · FDA recall Z-0981-2018 · Alden Optical
Hazard
Contact lenses lack sterility assurance. · FDA Class II
Units
3
Sold at
Worldwide Distribution - US Nationwide in the states:of CA, FL, GA, ID, IL, IN, KS, KY, MD, MI, MO, MS, NC, NJ, NM, NV, NY, OH, OR, PA, TX, VA, WI, WY and the country of Canada.
Description
Contact lenses lack sterility assurance.
Product
NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia) in aphakic and not aphakic persons with otherwise nondiseased eyes. The lens may be worn by persons who exhibit refractive astigmatism of 1.50 diopters or less where the astigmatism does not interfere with visual acuity.
Manufacturer(s)
Alden Optical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →