Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: Recalled by Vascular Technology, Inc. Due to Mislabeling

Date: June 19, 2018
Company: Vascular Technology, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Vascular Technology, Inc. directly.

Affected Products

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

Why Was This Recalled?

Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver

Where Was This Sold?

This product was distributed to 1 state: CA

Affected (1 state)Not affected

About Vascular Technology, Inc.

Vascular Technology, Inc. has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report