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 | Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product |
| Product | BVI Custom Eyes® Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584671 Ophthalmic surgical kits |
| Quantity | 214 kits |
| Distribution | Nationwide Distribution including KY, GA, MI, and NJ. |
| Initiated | 2015-05-01 |
| Classified | 2015-06-15 |
| Terminated | 2021-01-28 |
| Recall number | Z-1805-2015 |
| 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-1805-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71293/
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