FDA Issues Class I Recall of Zilver® PTX® Drug-Eluting Stent

Today the U.S. Food and Drug Administration issued a Class I recall of the Zilver PTX Drug-Eluting Peripheral Stent. One month ago, Cook Medical, the device manufacturer, issued its own voluntary recall. It was not immediately clear as to why the FDA has now issued its own recall.
Source: News from Angioplasty.Org - Category: Cardiology Source Type: news