Alcon recalls specific TOTAL PLUS 25+ 10K VALVE STD ophthalmic knives due to reported sharpness issues. Affected models have catalog number 8065752437 and lot numbers 16AUM5 through 16HYDT.
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 TOTAL PLUS 25+ 10K VALVE STD ophthalmic knives because they have been reported to be too sharp. This could cause injury during use by eye care professionals.
The knives have been reported to be too sharp, which could lead to injury during surgical procedures. This sharpness issue is specific to certain models and lot numbers.
Eye care professionals who use the recalled ophthalmic knives for procedures are most at risk. Patients using these knives during surgery may also be affected.
Check for the model catalog number 8065752437 on the knife. Affected items were sold with lot numbers 16AUM5, 16C9RE, 16DDFN, 16HE6A, 16HYDP, 16HYDR, or 16HYDT.
Inspect the knife for signs of excessive sharpness that could cause injury during use.
The recall is for specific ophthalmic knives used in surgery. If you have the recalled model, contact Alcon for guidance.
Check the catalog number on the knife; affected models have 8065752437 and lot numbers 16AUM5 through 16HYDT.
The recall does not specify a remedy, so contact Alcon directly for advice on safe handling or disposal.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2676-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2676-2024 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.
