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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

June 28, 2024

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

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Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

March 21, 2024

Medtronic Recalls Batteries in Some HeartWare VAD Systems

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Medtronic Recalls Batteries in Some HeartWare VAD Systems

June 23, 2022

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

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Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

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FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

June 03, 2021

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

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CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

July 01, 2020

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HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

May 23, 2018

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HeartMate II Left Ventricular Assist System Under Recall Due to Controller Exchange Problems

May 24, 2017

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