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FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

Todd Neale

December 05, 2025

News Conference News ACC 2025

By 2 Years, Tricuspid TEER Reduces Hospitalizations for HF: TRILUMINATE

Michael O'Riordan

March 31, 2025

News Conference News AHA 2024

Novel AI-Based, Noninvasive Sensor Can Accurately Measure PCWP in HFrEF

Yael L. Maxwell

November 25, 2024

News Daily News

FDA Approves Dropping Aspirin for HeartMate 3 LVAD Patients

L.A. McKeown

August 21, 2024

News Daily News

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Todd Neale

June 28, 2024

News Daily News

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

L.A. McKeown

May 15, 2024

News Conference News ESC Heart Failure 2024

SEQUOIA-HCM: Aficamten Boosts Exercise Capacity in Obstructive HCM

Michael O'Riordan

May 13, 2024

News Daily News

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

Caitlin E. Cox

April 22, 2024

News Conference News ACC 2024

Most HFrEF Patients Eligible for Quadruple Therapy, but Few Get It

Michael O'Riordan

March 27, 2024

News Conference News THT 2024

Small Study Hints at Potential for HF Bone Marrow Cell Therapy: CardiAMP-HF

Michael O'Riordan

March 08, 2024

News Conference News THT 2024

Debating the Role of T-TEER in the Sickest Patients

Michael O'Riordan

March 05, 2024

News Daily News

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

Caitlin E. Cox

August 18, 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

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox

July 27, 2023

News Features

Myriad Novel Devices Aim to Boost Decongestion in Acute HF

Todd Neale

April 10, 2023

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

Second Recall in Less Than 2 Months for Cardiosave IABPs

L.A. McKeown

March 17, 2023

News Daily News

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

Shelley Wood

January 25, 2023

News Daily News

FDA Advisors Recommend Against Approval of Omecamtiv Mecarbil

Michael O'Riordan

December 14, 2022

News Daily News

Medtronic Recalls Batteries in Some HeartWare VAD Systems

L.A. McKeown

June 23, 2022

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FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

By 2 Years, Tricuspid TEER Reduces Hospitalizations for HF: TRILUMINATE

Novel AI-Based, Noninvasive Sensor Can Accurately Measure PCWP in HFrEF

FDA Approves Dropping Aspirin for HeartMate 3 LVAD Patients

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

SEQUOIA-HCM: Aficamten Boosts Exercise Capacity in Obstructive HCM

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

Most HFrEF Patients Eligible for Quadruple Therapy, but Few Get It

Small Study Hints at Potential for HF Bone Marrow Cell Therapy: CardiAMP-HF

Debating the Role of T-TEER in the Sickest Patients

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

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

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Myriad Novel Devices Aim to Boost Decongestion in Acute HF

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Second Recall in Less Than 2 Months for Cardiosave IABPs

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

FDA Advisors Recommend Against Approval of Omecamtiv Mecarbil

Medtronic Recalls Batteries in Some HeartWare VAD Systems

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