Alcon recalls specific ClearCut Safety Intrepid DB2.2 ophthalmic knives due to reported sharpness issues. Affected models include 8065772265 with lot numbers 15P7RH, 15P7RK, 15TFMJ, 15V034.
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 specific ClearCut Safety Intrepid DB2.2 ophthalmic knives because they have been reported to be too sharp. This could cause injury during eye surgery procedures if not handled carefully.
The knives have been reported to be too sharp, which could lead to injury during eye surgery procedures. This sharpness issue may occur if the knife is not properly handled or maintained.
Ophthalmologists and eye care professionals who use the recalled ClearCut Safety Intrepid DB2.2 ophthalmic knives are affected. Those with the specific model and lot numbers listed are most at risk.
Check for the model number 8065772265 on the knife. Affected lot numbers include 15P7RH, 15P7RK, 15TFMJ, and 15V034. The product is an ophthalmic knife used in eye surgery.
Verify the model number and lot numbers listed in the recall notice to confirm if your knife is affected.
Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Safety Intrepid DB2.2 ophthalmic knives.
The affected model number is 8065772265 with lot numbers 15P7RH, 15P7RK, 15TFMJ, and 15V034.
The recall does not require immediate stop use; however, affected users should check the product details to confirm if their knife is affected.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2651-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2651-2024 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.
