Alcon recalls specific ophthalmic knives due to reported sharpness issues. Affected models include 25+ CMB PAK 7.5CPM,V,STD 0.9 with catalog number 8065751767. Consumers should check lot numbers for affected items.
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 ophthalmic knives that have been reported to be too sharp. This could pose a risk of injury during use by eye care professionals. Affected models include the 25+ CMB PAK 7.5CPM,V,STD 0.9 with catalog number 8065751767.
The knives have been reported to be too sharp, which could lead to injury if mishandled during eye procedures. This sharpness issue is specific to certain models and lot numbers.
Eye care professionals using the specific ophthalmic knives with catalog number 8065751767 are most at risk. The recall affects models sold with lot numbers 16C9ND, 16C9NE, 16C9NF, 16HE5R, and 16HYDK.
Check for the model name '25+ CMB PAK 7.5CPM,V,STD 0.9' and catalog number 8065751767. Affected items have lot numbers 16C9ND, 16C9NE, 16C9NF, 16HE5R, or 16HYDK.
Identify the model number and lot numbers 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 use.
The affected models are the 25+ CMB PAK 7.5CPM,V,STD 0.9 with catalog number 8065751767.
Check for the model name '25+ CMB PAK 7.5CPM,V,STD 0.9', catalog number 8065751767, and lot numbers 16C9ND, 16C9NE, 16C9NF, 16HE5R, or 16HYDK.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2675-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2675-2024 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.
