Home / Recalls / Medical Devices
Alden Optical recalls Alden HP54 Sphere Daily Wear Soft contact; Catalog Number: AOHPS54 Product Usage: The ALDEN SPHERE LENS for daily we
Recalled March 21, 2018 · FDA recall Z-0985-2018 · Alden Optical
Hazard
Contact lenses lack sterility assurance. · FDA Class II
Units
2
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
Alden HP54 Sphere Daily Wear Soft contact; Catalog Number: AOHPS54 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia). 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 →