Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cordis Angiographic Catheter Extensions. Used to transport fluid from the Recalled by Cordis US Corp Due to There is a potential for separation at the...
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 Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Quantity: 16,950 units (2,915 US and 14,000 OUS)
Why Was This Recalled?
There is a potential for separation at the male connector.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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