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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

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

News Daily News

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

August 18, 2023

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: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

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FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

Yael L. Maxwell

April 12, 2021

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FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

January 13, 2020

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

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FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

Michael O'Riordan

January 17, 2018

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FDA Expands Indications for Two Endovascular Stroke Therapies

September 06, 2016

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FDA:凝血监测系统四面楚歌、境况堪忧

July 13, 2016

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FDA: No More Chances for Embattled Coagulation Monitoring System

July 13, 2016

News Daily News

FDA: No Más Oportunidades para el Acosado Sistema para Monitorizar la Coagulación

July 13, 2016

News Daily News

Los Episodios Cardíacos Serios, incluida la Muerte se asocian a un Abuso del Fármaco Antidiarréico Lorepamida

Michael O'Riordan

June 08, 2016

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