Alcon recalls specific ClearCut HP2 DB SLIT 3.2MM ANGCE ophthalmic knives due to sharpness complaints. Affected models have catalog number 8065983265 and lot numbers 16JV6H, 16DFL3.
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 HP2 DB SLIT 3.2MM ANGCE ophthalmic knives after reports of sharpness issues. This could lead to injury if the knife is used improperly.
The knives have been reported to be too sharp, which could cause injury if mishandled during surgical procedures. This sharpness issue is related to the specific model and lot numbers.
Ophthalmic surgeons and medical professionals who use the ClearCut HP2 DB SLIT 3.2MM ANGCE knives. Those with the specific catalog number 8065983265 and lot numbers 16JV6H or 16DFL3 are most at risk.
Check for the catalog number 8065983265 and lot numbers 16JV6H or 16DFL3 on the product label. The product is an ophthalmic knife used in eye surgery.
Look for the catalog number 8065983265 and lot numbers 16JV6H or 16DFL3 on the knife's label.
The specific model number is CLEARCUT HP2 DB SLIT 3.2MM ANGCE with catalog number 8065983265.
Lot numbers 16JV6H and 16DFL3 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2660-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2660-2024 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.
