VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref — Class II medical device recall Z-3026-2018
Terminated recall by Vascular Technology, Inc., reported 2018-09-19, distributed in CA. Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
| Recall number | Z-3026-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vascular Technology, Inc., Nashua, NH, United States |
| Recall initiated | 2018-06-19 |
| Classified | 2018-09-12 |
| Reported by FDA | 2018-09-19 |
| Terminated | 2020-01-30 |
| Distributed | CA |
| Quantity | 10 units |
| Reason classes | labeling |
| Serial numbers | 14329-001, 14329-002, 14329-003, 14329-004, 14329-005, 14329-006, 14329-007, 14329-008, 14329-009, 14329-010 |
| Model numbers | 108910 |
Product
VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.
Reason for recall
Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3026-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.