FDA Class I Recall for HeartMate 3 Left Ventricular Assist System FDA Class I Recall for HeartMate 3 Left Ventricular Assist System

The FDA issued a Class I recall for the left ventricular assist system because of a potential malfunction that may lead to graft occlusion.Medscape Medical News

Source: Medscape Medical News Headlines - May 22, 2018 Category: Consumer Health News Tags: Cardiology News Alert Source Type: news