FDA Class I Recall for Medtronic HeartWare VAD FDA Class I Recall for Medtronic HeartWare VAD

The recall, affecting more than 200,000 devices, is due to the possibility of interruption in the electrical connection between the system ' s power source and the HVAD controller.News Alerts

Source: Medscape Medical News Headlines - June 1, 2018 Category: Consumer Health News Tags: Cardiology News Alert Source Type: news