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 | Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly labeled shelf carton. |
| Product | Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmic surgery. |
| Quantity | 440 |
| Distribution | Distribution to US states of CA, IL, MD, MN, NJ, OH & PA; and Israel |
| Initiated | 2018-06-18 |
| Classified | 2018-08-09 |
| Terminated | 2019-10-30 |
| Recall number | Z-2740-2018 |
| 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-2740-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80565/
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