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News Daily News

FDA: Another Class I Recall for HeartWare VAD

Shelley Wood

April 16, 2021

News Daily News

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

Yael L. Maxwell

April 12, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

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

Michael O'Riordan

February 12, 2021

News Daily News

Medtronic Recalls Parts of Its HeartWare VAD System

Todd Neale

May 29, 2020

News Daily News

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

L.A. McKeown

May 01, 2020

News Daily News

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

L.A. McKeown

April 07, 2020

News Daily News

FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology

Caitlin E. Cox

March 31, 2020

News Daily News

FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

Shelley Wood

February 24, 2020

News Daily News

FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

Todd Neale

January 13, 2020

News Features

TCTMD Looks Back on 5 Years of Its Kahn Journalism Fellowship

L.A. McKeown

December 26, 2019

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

L.A. McKeown

December 17, 2019

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown

October 28, 2019

News Daily News

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for August 2019

Shelley Wood

August 30, 2019

News Daily News

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

Todd Neale

August 28, 2019

News Daily News

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

News Features

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

Marcus A. Banks

August 15, 2019

News Daily News

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

Shelley Wood

August 05, 2019

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FDA: Another Class I Recall for HeartWare VAD

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

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

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

Medtronic Recalls Parts of Its HeartWare VAD System

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology

FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

TCTMD Looks Back on 5 Years of Its Kahn Journalism Fellowship

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

FDA: Class I Recall for CentriMag Circulatory Support System Motor

FDA: New Concerns Surface With Endologix Grafts for AAA

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

TCTMD’s Top 10 Most Popular Stories for August 2019

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

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

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