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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 Daily News

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

Caitlin E. Cox

April 22, 2024

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for March 2024

Shelley Wood

April 03, 2024

News Opinion Off Script

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Sanjay Kaul, MD

March 29, 2024

News Opinion Off Script

My Hopes for Cardiology in 2024: More Honesty, Humility, and Collaboration

Benoy Shah, MBBS, MD(Res)

January 24, 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 Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2023

Shelley Wood

July 31, 2023

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2023

Shelley Wood

July 03, 2023

News Daily News

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

Caitlin E. Cox

June 05, 2023

News Features

Some Rays of Hope for ‘Sorry State’ of Transplant Rejection

Shelley Wood

May 08, 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

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

News Daily News

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

Michael O'Riordan

October 17, 2022

News Daily News

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

L.A. McKeown

August 19, 2022

News Daily News

Medtronic Recalls Batteries in Some HeartWare VAD Systems

L.A. McKeown

June 23, 2022

News Daily News

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

L.A. McKeown

April 29, 2022

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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

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

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

TCTMD’s Top 10 Most Popular Stories for March 2024

Evoque and Patisiran: A Tale of Two Regulatory Journeys

My Hopes for Cardiology in 2024: More Honesty, Humility, and Collaboration

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

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

TCTMD’s Top 10 Most Popular Stories for July 2023

TCTMD’s Top 10 Most Popular Stories for June 2023

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

Some Rays of Hope for ‘Sorry State’ of Transplant Rejection

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

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

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

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

Medtronic Recalls Batteries in Some HeartWare VAD Systems

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

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