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News Daily News

IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

L.A. McKeown

September 06, 2017

News Daily News

FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts

Michael O'Riordan

August 17, 2017

Studies Supporting Device Modifications Weak, Often Based on Surrogate Endpoints

News Daily News

FDA Clearance of Modified Devices Relies Heavily on Weak Studies, Surrogate Endpoints

Michael O'Riordan

August 16, 2017

News Daily News

FDA Deems ‘Field Action’ for Faulty IABPs a Class I Recall

Shelley Wood

August 07, 2017

News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Todd Neale

July 21, 2017

News Daily News

TCTMD’s Top 10 Most Popular Stories for June 2017

Shelley Wood

July 03, 2017

News Daily News

FDA: Class I Recall for Venture Catheters

L.A. McKeown

June 21, 2017

News Conference News TVT 2017

Reacting to REPRISE III: Enthusiasm, Explanations, and Caveats for the Lotus Pivotal TAVR Trial

Shelley Wood

June 16, 2017

News Daily News

Apixaban Recalled Following Complaints of Dose-Packaging Mismatch

Shelley Wood

June 13, 2017

News Industry News

AstraZeneca Initiates Voluntary Nationwide Recall of One Lot of BRILINTA 90mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle from That Lot

May 26, 2017

News Daily News

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

Todd Neale

May 24, 2017

News Daily News

Abbott Vascular Recalls Three Coronary Catheters Because of Possible Sheath Removal Problems

Todd Neale

May 16, 2017

REPRISE III: Lotus Valve Matches CoreValve in First Head-to-Head TAVR Trial

News Conference News EuroPCR 2017

REPRISE III: Lotus Valve Matches CoreValve in First, Large Head-to-Head TAVR Trial

Shelley Wood

May 16, 2017

News Daily News

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

L.A. McKeown

March 24, 2017

News Conference News ACC 2017

Live From Washington: ACC 2017, Day Three

Shelley Wood

March 19, 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for February 2017

Shelley Wood

March 01, 2017

News Daily News

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

L.A. McKeown

January 31, 2017

News Daily News

Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’

L.A. McKeown

January 11, 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular News and Features for 2016

Shelley Wood

December 29, 2016

News Daily News

FDA: Class I Recall for FindrWIRZ Guidewire System

Shelley Wood

November 22, 2016

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IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts

FDA Clearance of Modified Devices Relies Heavily on Weak Studies, Surrogate Endpoints

FDA Deems ‘Field Action’ for Faulty IABPs a Class I Recall

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

TCTMD’s Top 10 Most Popular Stories for June 2017

FDA: Class I Recall for Venture Catheters

Reacting to REPRISE III: Enthusiasm, Explanations, and Caveats for the Lotus Pivotal TAVR Trial

Apixaban Recalled Following Complaints of Dose-Packaging Mismatch

AstraZeneca Initiates Voluntary Nationwide Recall of One Lot of BRILINTA 90mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle from That Lot

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

Abbott Vascular Recalls Three Coronary Catheters Because of Possible Sheath Removal Problems

REPRISE III: Lotus Valve Matches CoreValve in First, Large Head-to-Head TAVR Trial

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

Live From Washington: ACC 2017, Day Three

TCTMD’s Top 10 Most Popular Stories for February 2017

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’

TCTMD’s Top 10 Most Popular News and Features for 2016

FDA: Class I Recall for FindrWIRZ Guidewire System

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