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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

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

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

Yael L. Maxwell

June 18, 2019

TCTMD’s Top 10 Most Popular Stories for May 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for May 2019

May 31, 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 Provides Update on Poorer Survival With Impella RP in Postmarket Setting

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

May 21, 2019

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

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FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

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FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

TCTMD’s Top 10 Most Popular Stories for April 2019

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TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 2019

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

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Two Pediatric Cardiac Catheters Recalled for Defective Balloons

April 26, 2019

FDA Warns Against Off-label Use of Wingspan Stent System

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FDA Warns Against Off-label Use of Wingspan Stent System

April 25, 2019

FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

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FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

Michael O'Riordan

March 22, 2019

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

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FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

March 21, 2019

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

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

March 15, 2019

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

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FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

March 04, 2019

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

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Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

February 27, 2019

FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

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FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

February 22, 2019

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

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Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

February 19, 2019

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

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Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

February 15, 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

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