Home / Recalls / Medical Devices
Us Endovascular recalls USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO
Recalled April 20, 2016 · FDA recall Z-1362-2016 · Us Endovascular
Hazard
Product may kink during use rendering the product unusable. · FDA Class II
Units
843 catheters
Sold at
US Distribution to the states of : AR, CA, FL, LA, MO, MI, MS, NY, TN, and TX.
Description
Product may kink during use rendering the product unusable.
Product
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Manufacturer(s)
Us Endovascular
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →