FDA Device recall Z-3026-2018
VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref
- FDA Device
- Class II
- terminated
- Published 2018-09-19
On 2018-09-19 the FDA classified a Class II recall of VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref by Vascular Technology, citing device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3026-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-19 |
| Published | 2018-09-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Vascular Technology |
| Distribution | CA |
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
Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
Identifiers
| code_info | Serial Numbers: 14329-001, 14329-002, 14329-003, 14329-004, 14329-005, 14329-006, 14329-007, 14329-008, 14329-009, and 14329-010. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3026-2018%22
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