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December 16, 2024

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

Caitlin E. Cox

July 27, 2023

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Class I Recall for 350,000 Medtronic Defibrillators: FDA

July 19, 2023

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FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

July 11, 2023

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

Caitlin E. Cox

June 05, 2023

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

January 25, 2023

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

August 19, 2022

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Medtronic Recalls Batteries in Some HeartWare VAD Systems

June 23, 2022

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Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

Todd Neale

December 22, 2021

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FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

Yael L. Maxwell

April 12, 2021

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FDA: Class I Recall for HeartWare VAD Pump Implant Kit

March 01, 2021

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FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

February 12, 2021

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CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale

July 01, 2020

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FDA Expands TAVR Indication to Low-Risk Patients

August 16, 2019

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FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

August 05, 2019

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FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

May 07, 2019

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TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 2019

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FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

March 22, 2019

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FDA Touts Increased Oversight of Medical Device Makers