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Some Mitral TEER Patients Slipping Through the Cracks in the First Month

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Some Mitral TEER Patients Slipping Through the Cracks in the First Month

Michael O'Riordan

March 21, 2025

Repeat Rejection Still a Problem After Pediatric Heart Transplant

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Repeat Rejection Still a Problem After Pediatric Heart Transplant

October 23, 2024

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

June 28, 2024

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

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

August 18, 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

Global Numbers Paint Grim Picture of GDMT Uptake, Costs, and HF Outcomes

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Global Numbers Paint Grim Picture of GDMT Uptake, Costs, and HF Outcomes

Michael O'Riordan

June 23, 2023

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

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Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

June 05, 2023

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

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Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

March 31, 2023

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

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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

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Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

Impella RP Mortality Rate No Longer a Concern, FDA Says

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Impella RP Mortality Rate No Longer a Concern, FDA Says

December 05, 2022

AI Accurately Detects LV Dysfunction Using Single-Lead Apple Watch ECG

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AI Accurately Detects LV Dysfunction Using Single-Lead Apple Watch ECG

November 17, 2022

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

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

Michael O'Riordan

October 17, 2022

FDA: Class I Recall of Cobalt and Crome ICDs and CRT-Ds Due to Reduced-Energy Shock

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FDA: Class I Recall of Cobalt and Crome ICDs and CRT-Ds Due to Reduced-Energy Shock

August 19, 2022

Medtronic Recalls Batteries in Some HeartWare VAD Systems

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Medtronic Recalls Batteries in Some HeartWare VAD Systems

June 23, 2022

DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

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DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

May 05, 2022

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

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Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

April 29, 2022

FDA Investigating Possible Sex Differences in LAAO Outcomes

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FDA Investigating Possible Sex Differences in LAAO Outcomes

September 27, 2021

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

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FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

June 03, 2021

FDA: Another Class I Recall for HeartWare VAD

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FDA: Another Class I Recall for HeartWare VAD

April 16, 2021

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