FDAFebruary 11, 2016device
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Product may kink during use rendering the product unusable.
What to do
FDA enforcement status: Terminated
Brands named
us endovascular
Recall history
No related federal recalls on record for this brand yet.
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