Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Recalled by Us Endovascular Due to Product may kink during use rendering the product...
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 Us Endovascular directly.
Affected Products
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Quantity: 843 catheters
Why Was This Recalled?
Product may kink during use rendering the product unusable.
Where Was This Sold?
This product was distributed to 10 states: AR, CA, FL, LA, MI, MS, MO, NY, TN, TX
About Us Endovascular
Us Endovascular has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report