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News Daily News

FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

Yael L. Maxwell

October 25, 2019

News Daily News

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

Michael O'Riordan

October 09, 2019

News Daily News

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

Michael O'Riordan

August 22, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

News Daily News

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

Shelley Wood

August 05, 2019

News Daily News

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

Marcus A. Banks

July 24, 2019

News Daily News

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

Shelley Wood

July 22, 2019

News Daily News

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

Yael L. Maxwell

June 18, 2019

News Daily News

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

L.A. McKeown

May 30, 2019

News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

Todd Neale

April 25, 2019

News Daily News

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

L.A. McKeown

March 15, 2019

News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

Todd Neale

February 27, 2019

News Daily News

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

Caitlin E. Cox

February 04, 2019

News Conference News ISET 2019

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

Caitlin E. Cox

January 28, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2018

Shelley Wood

November 30, 2018

News Daily News

FDA Touts Increased Oversight of Medical Device Makers

Michael O'Riordan

November 22, 2018

News Daily News

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

Michael O'Riordan

November 06, 2018

News Daily News

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

L.A. McKeown

October 16, 2018

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FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

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

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

FDA Expands TAVR Indication to Low-Risk Patients

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

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

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

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

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

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

TCTMD’s Top 10 Most Popular Stories for April 2019

FDA Warns Against Off-label Use of Wingspan Stent System

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

TCTMD’s Top 10 Most Popular Stories for November 2018

FDA Touts Increased Oversight of Medical Device Makers

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

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