Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis Corporation Due to Inability to deploy the stent or partial stent...
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 Cordis Corporation directly.
Affected Products
Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)
Quantity: 4,400 units in US and 3,100 units in Foreign Countries
Why Was This Recalled?
Inability to deploy the stent or partial stent deployment.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cordis Corporation
Cordis Corporation has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report