Alcon recalls specific ClearCut Sideport Knives due to sharpness complaints. Affected models may cause injury if used improperly. Contact Alcon for details.
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.
Alcon is recalling certain ClearCut Sideport Knives because users have reported sharpness issues that could lead to injury. This recall affects specific model numbers and requires customers to check if their knife is affected.
The knives have been reported to be too sharp, which could cause injury if mishandled during surgical procedures. This sharpness issue is linked to complaints from medical professionals using the product.
Ophthalmic surgeons and medical professionals who use the ClearCut Sideport Knife Dual Bevel 1.2mm Angled model are most at risk. The recall applies to specific model numbers sold between 2023 and 2024.
Check for the model number 8065982465 on the knife. The recall applies to knives sold with lot number 169L42 between 2023 and 2024.
Look for the model number 8065982465 on the knife's packaging or blade.
Reach out to Alcon Research LLC for assistance with the recall process.
The recall is due to sharpness complaints, but the knives are not inherently dangerous. Medical professionals report issues with the sharpness that could lead to injury if mishandled.
Check for the model number 8065982465 and lot number 169L42 on the knife. The recall applies to specific models sold between 2023 and 2024.
Contact Alcon Research LLC directly for guidance on the recall process. They will provide instructions based on your specific model.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2658-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2658-2024 from Alcon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
