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FDA Said Medtronic Conducted Recall of Heartware Ventricular Assist Device System to Inform Health Care Providers, Patients of Battery Performance Issues; Provided Information About HVAD System's Battery Electrical Faults Caused by Interaction Between Bat

FDA Said Medtronic Conducted Recall of Heartware Ventricular Assist Device System to Inform Health Care Providers, Patients of Battery Performance Issues; Provided Information About HVAD System's Battery Electrical Faults Caused by Interaction Between Bat

FDA表示，美敦力召回了心脏辅助装置系统，以告知医护人员和患者电池性能问题；提供了BAT之间相互作用导致的HVAD系统电池电气故障的信息
Benzinga Real-time News ·  2022/07/01 03:45

FDA Said Medtronic Conducted Recall of Heartware Ventricular Assist Device System to Inform Health Care Providers, Patients of Battery Performance Issues; Provided Information About HVAD System's Battery Electrical Faults Caused by Interaction Between Battery Software and Internal Component

FDA表示，美敦力召回了心脏辅助装置系统，以告知医护人员和患者电池性能问题；提供了由于电池软件和内部组件相互作用而导致的HVAD系统电池电气故障的信息

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