Alcon recalls 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU models with catalog number 8065000095 due to reported sharpness issues. Affected units may have increased risk of injury during ophthalmic procedures.
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 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU ophthalmic knives with model number 8065000095 because they have been reported to be too sharp. This could lead to injury during eye surgery procedures if not handled carefully.
The recalled ophthalmic knives have been reported to be too sharp, which could cause injury during eye surgery. This sharpness issue may lead to cuts or other injuries if the knives are not handled with extreme care.
Ophthalmic surgeons and medical professionals using the recalled knives for eye procedures are most at risk. Patients undergoing surgery with these knives may also face injury risks.
Check for model number 8065000095 on the product. The affected units were sold with lot numbers 16D1KR through 16HYE1. This recall applies to 25+ specific ophthalmic knives.
Look for model number 8065000095 on the knife packaging or label.
Reach out to Alcon Research LLC for guidance on handling the recalled product.
The recall indicates reported sharpness issues, so they may pose a risk during eye surgery. Use with caution until Alcon provides further instructions.
Check for model number 8065000095 and lot numbers 16D1KR through 16HYE1 on the product label.
Contact Alcon Research LLC directly for specific instructions on handling the product.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2671-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2671-2024 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.
