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

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

December 17, 2019

FDA: New Concerns Surface With Endologix Grafts for AAA

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FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

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

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

Michael O'Riordan

August 22, 2019

FDA Expands TAVR Indication to Low-Risk Patients

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FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

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

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

Marcus A. Banks

July 24, 2019

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

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

July 22, 2019

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

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

July 02, 2019

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

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

May 30, 2019

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

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

February 04, 2019

TCTMD’s Top 10 Most Popular Stories for January 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for January 2019

January 31, 2019

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