Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX Recalled by Micro Therapeutics, Inc. Due to Due to incorrect size and configuration labeling of...
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 Micro Therapeutics, Inc. directly.
Affected Products
AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;
Quantity: 96 systems
Why Was This Recalled?
Due to incorrect size and configuration labeling of the detachable coil system.
Where Was This Sold?
International distribution in the countries of China and Republic of Korea.
About Micro Therapeutics, Inc.
Micro Therapeutics, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report