Alcon recalls specific ClearCut SatinSlit Full Handle ophthalmic knives due to reported sharpness issues. Affected models include 8065993045 with lot numbers 164RXE and 16F1PX. Consumers should check their product details and contact Alcon for guidance.
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 SatinSlit Full Handle ophthalmic knives (model 8065993045) because they have been reported to be too sharp, which could cause injury during use. This recall affects ophthalmic surgeons and medical professionals who use these knives in eye procedures.
The knives have been reported to be too sharp, which could lead to injury if mishandled during eye surgery. This sharpness issue is a concern because ophthalmic knives are used in delicate procedures where precision is critical.
Ophthalmic surgeons and medical professionals who use these specific ClearCut SatinSlit Full Handle ophthalmic knives for eye procedures are most at risk. The recall applies to models with lot numbers 164RXE and 16F1PX.
Check for the model number 8065993045 on the product. Lot numbers 164RXE and 16F1PX are associated with this recall. The product is an ophthalmic knife used in eye surgery.
Identify the model number (8065993045) and lot numbers (164RXE, 16F1PX) to confirm if your knife is affected.
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.
Check the model number and lot numbers to see if your knife is affected. If it is, contact Alcon for guidance.
The recall record does not mention a specific remedy or fix for this issue.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2669-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2669-2024 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.
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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.
