Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: Recalled by Alcon Research LLC Due to Alcon has detected an increase in complaint reports...
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
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Quantity: 19,867 units
Why Was This Recalled?
Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance Ophthalmic knives.
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