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Coronary CTA Reimbursement for US Hospitals to Double in 2025

News Daily News

Coronary CTA Reimbursement for US Hospitals to Double in 2025

Yael L. Maxwell

November 08, 2024

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

May 08, 2024

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

News Daily News

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

Michael O'Riordan

September 15, 2023

Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

News Daily News

Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

August 17, 2023

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

News Daily News

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

Michael O'Riordan

August 10, 2023

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

March 31, 2023

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

News Daily News

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

January 25, 2023

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

A Simple Nudge Moves the Needle on Statin Prescribing

News Daily News

A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan

December 02, 2022

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

News Daily News

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

Michael O'Riordan

October 17, 2022

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

News Daily News

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

December 22, 2021

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

March 01, 2021

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

News Daily News

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

May 06, 2020

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

News Daily News

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

May 01, 2020

News Daily News

FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

January 13, 2020

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

News Daily News

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

News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

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

News Daily News

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

March 04, 2019

More INR Test Strips Recalled Due to Inaccurately High Results

News Daily News

More INR Test Strips Recalled Due to Inaccurately High Results

December 21, 2018

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