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 | Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver |
| Product | VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular. |
| Quantity | 10 units |
| Distribution | US Distribution to state of: CA. |
| Initiated | 2018-06-19 |
| Classified | 2018-09-12 |
| Terminated | 2020-01-30 |
| Recall number | Z-3026-2018 |
| 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 — Vascular Technology, Inc. (Z-3026-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80527/
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