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TCTMD Looks Back on 5 Years of Its Kahn Journalism Fellowship

News Features

TCTMD Looks Back on 5 Years of Its Kahn Journalism Fellowship

December 26, 2019

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

December 17, 2019

FDA: Class I Recall for CentriMag Circulatory Support System Motor

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

November 07, 2019

FDA: New Concerns Surface With Endologix Grafts for AAA

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

News Daily News

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

TCTMD’s Top 10 Most Popular Stories for August 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for August 2019

August 30, 2019

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

News Daily News

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

August 28, 2019

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

News Daily News

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

News Features

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

Marcus A. Banks

August 15, 2019

FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

News Daily News

FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

August 05, 2019

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

News Daily News

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

Marcus A. Banks

July 24, 2019

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

July 02, 2019

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

News Daily News

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell

June 18, 2019

Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

News Daily News

Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

May 30, 2019

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

News Daily News

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

April 26, 2019

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

News Daily News

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

March 04, 2019

TCTMD’s Top 10 Most Popular Stories for February 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for February 2019

March 01, 2019

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

February 27, 2019

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

News Daily News

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

February 15, 2019

No Excuses: Routine, High-Volume Exercise in Men Not Associated With Increased Mortality

News Daily News

No Excuses: Routine, High-Volume Exercise in Men Not Associated With Increased Mortality

Michael O'Riordan

February 01, 2019

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