Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is Recalled by MICROVENTION INC. Due to Due to inadvertently shipping to U.S. customers with...
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 MICROVENTION INC. directly.
Affected Products
VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
Quantity: N/A
Why Was This Recalled?
Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MICROVENTION INC.
MICROVENTION INC. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report