Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MultiLab Series II REVO non-invasive vascular diagnostic device Recalled by Unetixs Vascular, Inc. Due to The current luer fittings and adaptors allow for...
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 Unetixs Vascular, Inc. directly.
Affected Products
MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01
Quantity: 984 units
Why Was This Recalled?
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Unetixs Vascular, Inc.
Unetixs Vascular, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report