Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artix MT Thrombectomy Device Recalled by Inari Medical - Oak Canyon Due to Thrombectomy device specifies vessel range of 2.5-6 mm...
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 Inari Medical - Oak Canyon directly.
Affected Products
Artix MT Thrombectomy Device, REF: 32-102
Quantity: 45
Why Was This Recalled?
Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Inari Medical - Oak Canyon
Inari Medical - Oak Canyon has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report