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FDA Drops REMS Requirement for Antihypertensive Aprocitentan

Michael O'Riordan

April 09, 2025

News Conference News ACC 2025

DETECT-AS: Alert System Increases AV Replacement in Eligible Patients

Michael O'Riordan

April 04, 2025

News Daily News

Biden White House Delays Decision on Menthol Ban

Michael O'Riordan

December 07, 2023

News Daily News

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

Michael O'Riordan

September 15, 2023

News Daily News

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

Michael O'Riordan

August 10, 2023

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

News Daily News

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Michael O'Riordan

March 28, 2023

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

News Daily News

A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan

December 02, 2022

News Daily News

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

Michael O'Riordan

October 17, 2022

News Conference News AHA 2021

Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF

Michael O'Riordan

November 19, 2021

News Daily News

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Michael O'Riordan

September 23, 2021

News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

News Daily News

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

News Conference News

ACC, EHRA Cancel 2020 Meetings Over COVID-19

Michael O'Riordan

March 09, 2020

News Daily News

European Regulators Approve First Transcatheter MV Replacement Device

Michael O'Riordan

January 30, 2020

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 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

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FDA Drops REMS Requirement for Antihypertensive Aprocitentan

DETECT-AS: Alert System Increases AV Replacement in Eligible Patients

Biden White House Delays Decision on Menthol Ban

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

A Simple Nudge Moves the Needle on Statin Prescribing

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

ACC, EHRA Cancel 2020 Meetings Over COVID-19

European Regulators Approve First Transcatheter MV Replacement Device

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

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

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