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December 17, 2019

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VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

Todd Neale

November 20, 2019

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FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

November 14, 2019

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FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

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FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

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FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

Yael L. Maxwell

October 25, 2019

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

October 09, 2019

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

August 22, 2019

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FDA Expands TAVR Indication to Low-Risk Patients

August 16, 2019

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

August 05, 2019

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

Marcus A. Banks

July 24, 2019

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

July 22, 2019

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

July 02, 2019

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

Yael L. Maxwell

June 18, 2019

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

May 30, 2019

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

Todd Neale

May 21, 2019

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FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

May 08, 2019

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FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

May 07, 2019

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TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 2019

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Two Pediatric Cardiac Catheters Recalled for Defective Balloons