Alcon recalls specific ClearCut Sideport Knife Dual Bevel models due to increased reports of sharpness issues. Affected units have model numbers starting with 8065921541 and were sold in 2015-2016. Consumers should check their product details.
Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance Ophthalmic knives.
Alcon is recalling specific models of ClearCut Sideport Knife Dual Bevel ophthalmic knives after receiving more complaints about sharpness. This could lead to injury during medical procedures if the knife is too sharp.
The knives have been reported to be too sharp, which could cause injury during eye surgery procedures. Sharpness issues might lead to accidental cuts or other complications if the knife is used improperly.
Ophthalmologists and eye care professionals who use the recalled ClearCut Sideport Knife Dual Bevel models. Those with the specific model numbers listed in the recall are most at risk.
Check if your knife has the model number starting with 8065921541. The product was sold between 2015 and 2016, and the specific lot/batch numbers are listed in the recall notice.
Look for the model number starting with 8065921541 on the knife or its packaging.
Alcon has detected an increase in complaints about the knife being too sharp, which could lead to injury during eye surgery.
The affected models have a model number starting with 8065921541 and specific lot/batch numbers listed in the recall notice.
No, the recall does not require stopping use immediately. However, you should check if your knife is affected and contact Alcon if needed.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-1923-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-1923-2024 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.
