Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
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 Alcon Research LLC directly.
Affected Products
Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYSTEM, UV w/BLUE LIGHT FILTER. 13.0mm. LENGTH, 6.0mm ANTERIOR ASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
Quantity: 84 units
Why Was This Recalled?
Incorrect IOL diopter
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alcon Research LLC
Alcon Research LLC has 59 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report