Alcon recalls specific ClearCut Slit Full Handle 2.75mm Ang Dua ophthalmic knives due to sharpness complaints. Affected models include 8065992747 with lot numbers 1636Y0 through 16AV0E.
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 Slit Full Handle 2.75mm Ang Dua ophthalmic knives because they have been reported to be too sharp. This could lead to injury if used improperly during eye surgery.
The knives have been reported to be too sharp, which could cause injury during eye surgery. This sharpness issue arises from the specific design and manufacturing of the knives, leading to potential cuts or lacerations.
Ophthalmic surgeons and medical professionals who use these specific ClearCut knives for eye procedures are most at risk. Patients undergoing surgery with these knives may also be affected.
Check for the model number 8065992747 on the knife. Lot numbers 1636Y0, 164RX6, 166E81, 166E82, 16ALX5, 16DNMV, 1618V6, and 16AM3U are also affected.
Look for the model number 8065992747 on the knife's packaging or label.
Reach out to Alcon Research LLC for further assistance or to confirm if your knife is affected.
Alcon has detected an increase in complaints about the knives being too sharp, which could lead to injury during eye surgery.
The affected model number is 8065992747 with lot numbers 1636Y0, 164RX6, 166E81, 166E82, 16ALX5, 16DNMV, 1618V6, and 16AM3U.
The recall does not require immediate discontinuation; however, you should check if your knife is affected and contact Alcon for guidance.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2667-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2667-2024 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.
