Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2649-2024 — Product Desc: Product Name: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

U.S. FDA — Device Enforcement · United States · 2024-07-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2649-2024
Date of alert
2024-07-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Alcon Research LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
8065771541
Reported risk: Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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