Medtronic Recall of Heartware HVAD Equipment Is Class I, Says FDA Medtronic Recall of Heartware HVAD Equipment Is Class I, Says FDA

Twelve deaths have been reported in association with ' wear and tear ' issues involving cable connections and other components of the company ' s Heartware Ventricular Assist Device.News Alerts

Source: Medscape Cardiology Headlines - April 16, 2021 Category: Cardiology Tags: Cardiology News Alert Source Type: news