Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cordis Recalled by Cordis US Corp Due to product mix-up; Vascular stent labeled as one size...
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 US Corp directly.
Affected Products
Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only
Quantity: 1 unit
Why Was This Recalled?
product mix-up; Vascular stent labeled as one size but contains a different size.
Where Was This Sold?
This product was distributed to 5 states: AZ, AR, FL, NJ, TN
About Cordis US Corp
Cordis US Corp has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report