Class II — Beaver Visitec International, Inc.
| Recalling firm | Beaver-Visitec International, Inc. |
|---|---|
| Registered facility | Beaver-Visitec International, Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | One lot of Part Number 373025, Xstar® Kojo Safety Slit Knife 2.5mm 45® bevel up, incorrectly contains a bevel down blade instead of a bevel up blade. |
| Product | Xstar Kojo Safety Slit Knife, 2.5mm 45® Bevel Up, Part Number 373025 |
| Quantity | 2160 units |
| Distribution | International Distribution to Japan. |
| Initiated | 2023-10-10 |
| Classified | 2024-01-04 |
| Recall number | Z-0633-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Beaver Visitec International, Inc. (Z-0633-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93555/
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