Circulatory Assist Unit FDA Alerts
FDA Alerts
Class 1 Recall: Medtronic HeartWare HVAD System Recalled Due to Unintended Intermittent Electrical Disconnection between The Power Source and The Controller
Fri Jun 08 2018read article
FDA Alerts
Class 1 Recall: HeartWare Recalls Ventricular Assist Device Controllers Due to Loose Connectors which may Prevent Alarm from Sounding and Pump Stops
Mon Oct 31 2016read article
FDA Alerts
Class 1 Recall: HeartWare Recalls Ventricular Assist Device Pumps Due to Contamination Causing Electrical Issues
Tue Oct 25 2016read article
FDA Alerts
Class 1 Recall: Serious Adverse Events with Implantable Left Ventricular Assist Devices (LVADs): FDA Safety Communication
Mon Aug 10 2015read article
FDA Alerts
Class 1 Recall: HeartWare Ventricular Assist System – Updated with Multiple Reasons for Recalls
Mon Jun 29 2015read article