Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact lenses lack sterility assurance.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Alden Optical directly.
Affected Products
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.
Quantity: 3
Why Was This Recalled?
Contact lenses lack sterility assurance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alden Optical
Alden Optical has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report