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 | Terminated |
| Reason | Products were packaged with incorrect labeling, |
| Product | Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549 |
| Quantity | 1025 |
| Distribution | US Nationwide and Canada |
| Initiated | 2018-02-26 |
| Classified | 2018-05-10 |
| Terminated | 2019-10-30 |
| Recall number | Z-1801-2018 |
| 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 International Inc. (Z-1801-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79915/
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