Class III — Beaver Visitec
| Recalling firm | Beaver-Visitec International, Inc. |
|---|---|
| Registered facility | Beaver-Visitec International, Inc (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | The product contains a misprinted expiration date on the peel pack. Both were printed as "180615", which is the lot number. The Lot number is correct. |
| Product | Micro Knife 5.0mm 30®, Part Number 0001522 The Beaver® Micro Knife 5.0mm 30® is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. . |
| Quantity | 97 boxes (10units/box) |
| Distribution | US Nationwide Distribution to states of : AL, AZ, CA, FL, ID, MN, MO, NY, OH, PA, and TX; and internationally to: Ireland and UK. |
| Initiated | 2019-02-19 |
| Classified | 2019-04-04 |
| Terminated | 2020-07-21 |
| Recall number | Z-1088-2019 |
| 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 III recall — Beaver Visitec (Z-1088-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82248/
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