Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cordis MAXI LD PTA Dilatation Catheter Recalled by Cordis Corporation Due to Product was manufactured utilizing an expired inner body.
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 MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Quantity: 21 units
Why Was This Recalled?
Product was manufactured utilizing an expired inner body.
Where Was This Sold?
This product was distributed to 5 states: AL, AZ, FL, MN, MO
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