# FDA recall Z-3026-2018

> **Vascular Technology, Inc.** · Class II · device recall initiated 2018-06-19.

## 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

## Distribution

US Distribution to state of: CA.

## Key facts

- **Recall number:** Z-3026-2018
- **Recalling firm:** Vascular Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-19
- **Report date:** 2018-09-19
- **Termination date:** 2020-01-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nashua, NH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3026-2018

## Citation

> AI Analytics. FDA recall Z-3026-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-3026-2018. Source: US FDA. Licensed CC0.

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