Home / Recalls / Medical Devices
Vascular Technology, Inc. recalls VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative
Recalled July 16, 2014 · FDA recall Z-2001-2014 · Vascular Technology
Hazard
Report of the product penetrating the sterile barrier; this could render the product unsterile. · FDA Class II
Units
25
Sold at
Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.
Description
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Product
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.
Manufacturer(s)
Vascular Technology, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →