Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for Recalled by Cordis Corporation Due to The product in the packaging is larger (both...
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
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Quantity: 680 units
Why Was This Recalled?
The product in the packaging is larger (both inner and outer diameter) than the labeling indicates.
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