FDA: Guidewires for Rotablator Atherectomy Catheter Recalled FDA: Guidewires for Rotablator Atherectomy Catheter Recalled

After receiving three serious adverse-event reports, including one patient death, from the wires fracturing and separating from the system, the company has recalled 600 units in the US. News Alerts

Source: theHeart.org - December 1, 2015 Category: Cardiology Tags: Cardiology News Alert Source Type: news