Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch & Lomb Surgical, Inc. Due to Lens was manufactured with incorrect raw material.
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 Bausch & Lomb Surgical, Inc. directly.
Affected Products
Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.
Quantity: 336 IOLs (283 IOLs in the US, 53 IOLs outside the US)
Why Was This Recalled?
Lens was manufactured with incorrect raw material.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bausch & Lomb Surgical, Inc.
Bausch & Lomb Surgical, Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report