FDA Slaps Class I Recall on Sapien 3 Ultra for TAVR FDA Slaps Class I Recall on Sapien 3 Ultra for TAVR

The class I recall of the transcatheter aortic valve replacement (TAVR) device follows an urgent field warning about burst balloons issued last month by device maker, Edwards Lifesciences.News Alerts
Source: Medscape Cardiology Headlines - Category: Cardiology Tags: Cardiology News Alert Source Type: news