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Medline Recalls Valve Pack Kits With Expired Cannulas

Yael L. Maxwell

September 16, 2025

News Daily News

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

Todd Neale

August 06, 2025

News Daily News

FDA Drops REMS Requirement for Antihypertensive Aprocitentan

Michael O'Riordan

April 09, 2025

News Daily News

Coronary CTA Reimbursement for US Hospitals to Double in 2025

Yael L. Maxwell

November 08, 2024

News Daily News

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

Caitlin E. Cox

March 21, 2024

News Daily News

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

Caitlin E. Cox

October 17, 2023

News Daily News

GLP-1 Meds Linked to 265 Reports to FDA of Suicidal Ideation: Reuters

Shelley Wood

September 28, 2023

News Daily News

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

L.A. McKeown

September 18, 2023

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 Daily News

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

L.A. McKeown

July 12, 2023

News Daily News

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

Todd Neale

February 27, 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

Medtronic Recalls Batteries in Some HeartWare VAD Systems

L.A. McKeown

June 23, 2022

News Daily News

Medtronic Recalls TurboHawk Plus Atherectomy System

Todd Neale

March 09, 2022

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood

February 17, 2021

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Medline Recalls Valve Pack Kits With Expired Cannulas

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

FDA Drops REMS Requirement for Antihypertensive Aprocitentan

Coronary CTA Reimbursement for US Hospitals to Double in 2025

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

GLP-1 Meds Linked to 265 Reports to FDA of Suicidal Ideation: Reuters

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

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

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

A Simple Nudge Moves the Needle on Statin Prescribing

Medtronic Recalls Batteries in Some HeartWare VAD Systems

Medtronic Recalls TurboHawk Plus Atherectomy System

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

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