Vascular Technology, Inc.: Medical Device Recall in 2018 - (Recall #: Z-3026-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.

Product Classification:

Class II

Date Initiated: June 19, 2018

Date Posted: September 19, 2018

Recall Number: Z-3026-2018

Event ID: 80527

Reason for Recall:

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

Status: Terminated

Product Quantity: 10 units

Code Information:

Serial Numbers: 14329-001, 14329-002, 14329-003, 14329-004, 14329-005, 14329-006, 14329-007, 14329-008, 14329-009, and 14329-010.

Distribution Pattern:

US Distribution to state of: CA.

Voluntary or Mandated:

Voluntary: Firm initiated