Search - tctmd.com

Displaying 41 - 60 of 123

Sort: Relevancy | Date

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

Yael L. Maxwell

April 12, 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

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

News Daily News

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale

July 01, 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 Conference News

ACC, EHRA Cancel 2020 Meetings Over COVID-19

Michael O'Riordan

March 09, 2020

News Daily News

FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns

Shelley Wood

February 14, 2020

News Daily News

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

Shelley Wood

January 14, 2020

News Daily News

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

L.A. McKeown

December 17, 2019

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown

October 28, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

News Daily News

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

Shelley Wood

July 22, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for May 2019

Caitlin E. Cox

May 31, 2019

News Daily News

FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

Todd Neale

May 21, 2019

Advertisement

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

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

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

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

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

ACC, EHRA Cancel 2020 Meetings Over COVID-19

FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

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

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

FDA: New Concerns Surface With Endologix Grafts for AAA

FDA Expands TAVR Indication to Low-Risk Patients

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

TCTMD’s Top 10 Most Popular Stories for May 2019

FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

Advertisement

Advertisement

Sign In

Forgot Your Password?

Search TCTMD

CME TITLE

Sign up for our newsletter

Search TCTMD

Submit an Event

Become a PREMIUM MEMBER or LOG IN to view exclusive content

REGISTER for free or LOG IN to view this content