Class II — Beaver Visitec
| Recalling firm | Beaver-Visitec International, Inc. |
|---|---|
| Registered facility | Beaver-Visitec International, Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Blades are loose in handles and may fall out due to non cured epoxy |
| Product | Safety Sideport Knife 1.0mm 45®, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery |
| Quantity | 1354 units |
| Distribution | US Nationwide in the states of CA, IA, CO, HI, IA, MD & TX |
| Initiated | 2018-05-14 |
| Classified | 2018-07-02 |
| Terminated | 2021-06-08 |
| Recall number | Z-2342-2018 |
| 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 (Z-2342-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80311/
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