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News Daily News

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

L.A. McKeown

June 03, 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

Caitlin E. Cox

May 03, 2021

News Daily News

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

Caitlin E. Cox

April 23, 2021

News Daily News

FDA: Another Class I Recall for HeartWare VAD

Shelley Wood

April 16, 2021

News Daily News

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

Yael L. Maxwell

April 12, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood

February 17, 2021

News Daily News

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

News Daily News

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Shelley Wood

December 16, 2020

News Daily News

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

L.A. McKeown

December 04, 2020

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

News Daily News

Recall for Mislabeled Cartons of Amiodarone, Tranexamic Acid Injections: FDA

Shelley Wood

September 01, 2020

News Daily News

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale

July 01, 2020

News Daily News

Cardiology Societies Unite to Condemn Racism and Health Inequality

L.A. McKeown

June 01, 2020

News Daily News

Medtronic Recalls Parts of Its HeartWare VAD System

Todd Neale

May 29, 2020

News Features

Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies

Shelley Wood

May 20, 2020

News Daily News

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

Shelley Wood

May 06, 2020

News Daily News

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

L.A. McKeown

May 01, 2020

News Daily News

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

L.A. McKeown

April 07, 2020

News Conference News

ACC, EHRA Cancel 2020 Meetings Over COVID-19

Michael O'Riordan

March 09, 2020

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FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

TCTMD’s Top 10 Most Popular Stories for April 2021

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

FDA: Another Class I Recall for HeartWare VAD

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

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Recall for Mislabeled Cartons of Amiodarone, Tranexamic Acid Injections: FDA

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Cardiology Societies Unite to Condemn Racism and Health Inequality

Medtronic Recalls Parts of Its HeartWare VAD System

Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

ACC, EHRA Cancel 2020 Meetings Over COVID-19

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