Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
07-150-12 MIZUHO Recalled by Vascular Technology, Inc. Due to Report of the product penetrating the sterile barrier;...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Vascular Technology, Inc. directly.
Affected Products
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.
Quantity: 34
Why Was This Recalled?
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Where Was This Sold?
Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.
About Vascular Technology, Inc.
Vascular Technology, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report