Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VTI BAYONET DOPPLER 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
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.
Quantity: 25
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