Beaver Visitec recalls Xstar Safety Slit Knives with incorrect blade bevel configuration that could cause improper use. Affected kits include CustomEye Numbers 584562, 5800109. No remedy specified in recall notice.
The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).
Beaver Visitec is recalling Xstar Safety Slit Knives with a wrong blade configuration that could lead to improper use. This recall is for specific CustomEye Kits with model numbers 584562 and 5800109. The issue does not pose a safety risk that requires immediate action.
The blade's bevel was installed backward in the package (bevel down instead of bevel up). This could lead to improper use if the knife is not configured correctly for the intended purpose. However, the recall does not indicate any actual injury risk.
Users of CustomEye Kits with model numbers 584562 and 5800109 are likely affected. The risk is minimal as the issue is a manufacturing error rather than a safety hazard.
Check for Xstar Safety Slit Knives with model number 378227 in CustomEye Kits numbered 584562, 5800109. The kit lot numbers are 6068524, 6068025, and 6068285.
Verify the model number on the knife and kit lot numbers to confirm if it's affected.
The recall states the blade configuration is wrong but does not indicate any safety risk requiring immediate action.
The recall does not specify a remedy, so no action is required beyond checking if you have the affected model.
CustomEye Kits with model numbers 584562 and 5800109 are affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2162-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2162-2024 from Beaver Visitec. 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.
