Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alcon LenSx Ophthalmic Laser Recalled by Alcon LenSx, Inc. Due to Alcon LenSx received reports of unexpected downward motion...
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 LenSx, Inc. directly.
Affected Products
Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation.
Quantity: 75
Why Was This Recalled?
Alcon LenSx received reports of unexpected downward motion of the gantry.
Where Was This Sold?
Worldwide Distribution.
About Alcon LenSx, Inc.
Alcon LenSx, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report