Class II — Vascular Technology, Inc.
| Recalling firm | VASCULAR TECHNOLOGY INCORPORATED |
|---|---|
| Registered facility | VASCULAR TECHNOLOGY INCORPORATED (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Report of the product penetrating the sterile barrier; this could render the product unsterile. |
| Product | VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow. |
| Quantity | 25 |
| Distribution | Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan. |
| Initiated | 2014-05-28 |
| Classified | 2014-07-07 |
| Terminated | 2016-02-11 |
| Recall number | Z-2001-2014 |
| 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 — Vascular Technology, Inc. (Z-2001-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68512/
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