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News Conference News ACC 2025

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

Michael O'Riordan

April 04, 2025

News Daily News

Coronary CTA Reimbursement for US Hospitals to Double in 2025

Yael L. Maxwell

November 08, 2024

News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

Todd Neale

May 08, 2024

News Daily News

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

Michael O'Riordan

September 15, 2023

News Daily News

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

Caitlin E. Cox

August 17, 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

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

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

Shelley Wood

January 25, 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 Daily News

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

Todd Neale

December 22, 2021

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 Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

Caitlin E. Cox

May 03, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

News Daily News

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

Shelley Wood

May 06, 2020

News Daily News

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

L.A. McKeown

May 01, 2020

News Daily News

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

Todd Neale

January 13, 2020

News Daily News

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

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

Coronary CTA Reimbursement for US Hospitals to Double in 2025

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

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

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

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

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

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

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

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

TCTMD’s Top 10 Most Popular Stories for April 2021

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

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

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

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

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

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