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News Daily News

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

L.A. McKeown

December 17, 2019

News Daily News

VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

Todd Neale

November 20, 2019

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown

October 28, 2019

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 IntraClude Intra-Aortic Occlusion Device

Shelley Wood

July 02, 2019

News Daily News

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

Yael L. Maxwell

June 18, 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

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

L.A. McKeown

May 30, 2019

News Daily News

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

Todd Neale

May 21, 2019

News Daily News

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 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

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

VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

FDA: Class I Recall for CentriMag Circulatory Support System Motor

FDA: New Concerns Surface With Endologix Grafts for AAA

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 IntraClude Intra-Aortic Occlusion Device

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

TCTMD’s Top 10 Most Popular Stories for May 2019

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

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

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

TCTMD’s Top 10 Most Popular Stories for April 2019

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