Alcon recalls specific ophthalmic knives due to sharpness complaints. Affected models include 25+ CMB PAK 10K CPM,V,WA 0.9 with catalog number 8065752451. Owners should check lot numbers for recall.
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 ophthalmic knives that have been reported to be too sharp. This could cause injury during use by eye care professionals. The recall affects certain models sold with specific lot numbers.
The knives have been reported to be too sharp, which could lead to injury if mishandled during eye procedures. This sharpness issue is a concern for professionals who use these tools regularly.
Eye care professionals using the specific ophthalmic knives with catalog number 8065752451 and lot numbers 16AUN4, 16AUN3, 16C9PX, 16C9PY, or 16C9R0 are most at risk.
Check for the catalog number 8065752451 and lot numbers 16AUN4, 16AUN3, 16C9PX, 16C9PY, or 16C9R0 on the product packaging or label.
Look for the catalog number 8065752451 and lot numbers 16AUN4, 16AUN3, 16C9PX, 16C9PY, or 16C9R0 on the product.
Alcon is recalling specific ophthalmic knives due to reports of sharpness issues that could cause injury.
The affected models have catalog number 8065752451 and lot numbers 16AUN4, 16AUN3, 16C9PX, 16C9PY, or 16C9R0.
The recall record does not specify a remedy, so check with Alcon directly for next steps.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2679-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2679-2024 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.