Vascular Technology, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2001-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Product Classification:

Class II

Date Initiated: May 28, 2014

Date Posted: July 16, 2014

Recall Number: Z-2001-2014

Event ID: 68512

Reason for Recall:

Report of the product penetrating the sterile barrier; this could render the product unsterile.

Status: Terminated

Product Quantity: 25

Code Information:

LOT NUMBER 11786-37683

Distribution Pattern:

Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated