Vascular Technology, Inc. recalls 07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and tr

Recalled July 16, 2014 · FDA recall Z-1998-2014 · Vascular Technology

Hazard

Report of the product penetrating the sterile barrier; this could render the product unsterile. · FDA Class II

Units

164

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

07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 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 →