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 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
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The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.
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Risk Disclaimer
The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.
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