Beaver Visitec recalls 2.6mm 45-degree bevel slit knives (model 373726) due to mislabeling in shipments. Affected units may have incorrect lot numbers on individual packages.
Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly labeled shelf carton.
Beaver Visitec is recalling a specific ophthalmic surgery knife model due to mislabeling in shipments. This means some packages have the wrong lot numbers, but the product itself is safe to use if labeled correctly.
The product has a mislabeling issue where some individual packages show the wrong lot numbers (374891 Lot 6001701 instead of 373726 Lot 6001700) within the correct shelf carton. This could lead to confusion during product identification but does not affect the knife's safety or function.
Ophthalmic surgeons and medical professionals who use this knife model are likely affected. Those who received the product with incorrect lot numbers on individual packages are at slightly higher risk.
Check for the model number 373726 on the shelf carton. Individual packages may show lot number 6001701 instead of 6001700. The product is for ophthalmic surgery use only.
Verify the model number on the shelf carton and individual package lot numbers.
No, the mislabeling does not affect the knife's safety or function. The product is safe to use if labeled correctly.
Check the model number and lot numbers on the shelf carton and individual packages. If they match the correct labels, no action is needed.
Look for model number 373726 on the shelf carton. Individual packages may show lot number 6001701 instead of 6001700.
We’ve drafted a message you can send Beaver Visite: 2.6mm Slit Knife to request your refund or repair — edit it as you like.
Subject: Recall Z-2740-2018 — Beaver Visite: 2.6mm Slit Knife Beaver Visite: 2.6mm Slit Knife Hello, I own a Beaver Visite: 2.6mm Slit Knife that is covered by recall Z-2740-2018 from Beaver Visite: 2.6mm Slit Knife. 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.
