Alcon recalls specific ophthalmic knives due to sharpness complaints. Affected models include A-OK SATINSLIT FULL HANDLE2.75MM ANG SG with catalog number 8065992761. 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 ophthalmic knives that have been reported as too sharp. This could lead to injury if used improperly. Affected products include the A-OK SATINSLIT FULL HANDLE2.75MM ANG SG model with catalog number 8065992761.
The knives have been reported as too sharp, which could cause injury if mishandled during surgical procedures. This sharpness issue may lead to cuts or lacerations if the knife is not used with proper care.
Ophthalmic surgeons and medical professionals who use the recalled knives. Those with the specific model and catalog number are most at risk.
Check for the model name 'A-OK SATINSLIT FULL HANDLE2.75MM ANG SG' and catalog number 8065992761. The product was sold with lot numbers 1636XM, 16EV4H, 1618VR, 167PWV, or 16J7VA.
Identify the model name and catalog number to confirm if your knife is affected.
Reach out to Alcon for further guidance on the recall and potential remedies.
The affected model is A-OK SATINSLIT FULL HANDLE2.75MM ANG SG with catalog number 8065992761.
Check for the model name and catalog number 8065992761, and verify the lot numbers 1636XM, 16EV4H, 1618VR, 167PWV, or 16J7VA.
Contact Alcon for guidance on the recall and potential next steps.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2668-2024 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2668-2024 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.
