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FDA Warns of Deaths, Stroke With Latest-Generation Total Artificial Heart

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FDA Warns of Deaths, Stroke Due to Power System Problems With Total Artificial Heart System

August 17, 2018

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

News Daily News

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan

July 20, 2018

FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

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FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

Michael O'Riordan

July 16, 2018

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

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FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

June 19, 2018

Class I Recall for Medtronic’s HeartWare HVAD System

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Class I Recall for Medtronic’s HeartWare HVAD System

Michael O'Riordan

June 04, 2018

News Daily News

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

May 23, 2018

‘Think Big, But Act Small’: Specialized A-fib Clinic Cuts Mortality

News Conference News HRS 2018

‘Think Big, But Act Small’: Specialized A-fib Clinic Cuts Mortality

May 18, 2018

Implantable Cardiac Monitor for High-Risk ACS Patients Wins FDA Approval

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Implantable Cardiac Monitor for High-Risk ACS Patients Wins FDA Approval

Michael O'Riordan

May 08, 2018

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

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FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

April 20, 2018

FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

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FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

April 17, 2018

Abciximab in ‘Short Supply’ Worldwide

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Abciximab in ‘Short Supply’ Worldwide

April 13, 2018

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

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Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

February 27, 2018

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

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Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

Michael O'Riordan

February 27, 2018

FDA: Clarithromycin Risks Persist in Patients With CAD

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FDA: Clarithromycin Risks Persist in Patients With CAD

February 26, 2018

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

Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

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Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

January 11, 2018

Biotin Supplements Can Interfere With Cardiac Troponin Tests: FDA

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Biotin Supplements Can Interfere With Cardiac Troponin Tests: FDA

Michael O'Riordan

November 28, 2017

TCTMD’s Top 10 Most Popular Stories for October 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for October 2017

October 29, 2017

Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early

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Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early

October 09, 2017

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

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FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

October 02, 2017

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