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Vascular Technology, Inc. recalls 07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and
Recalled July 16, 2014 · FDA recall Z-2000-2014 · Vascular Technology
Hazard
Report of the product penetrating the sterile barrier; this could render the product unsterile. · FDA Class II
Units
34
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
07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 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 →