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News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood

July 26, 2023

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

News Daily News

A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan

December 02, 2022

News Daily News

FDA, Abbott Warn of Potential MitraClip Locking Malfunctions

L.A. McKeown

September 09, 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

DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

L.A. McKeown

May 05, 2022

News Daily News

Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

L.A. McKeown

April 26, 2022

News Industry News

Cardiologs Unveils New Solution to Enable Use of Smartwatches for Remote Patient Monitoring

July 21, 2021

News Daily News

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

Caitlin E. Cox

April 23, 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 Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

News Daily News

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Shelley Wood

December 16, 2020

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 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 Conference News

ACC, EHRA Cancel 2020 Meetings Over COVID-19

Michael O'Riordan

March 09, 2020

News Daily News

European Regulators Approve First Transcatheter MV Replacement Device

Michael O'Riordan

January 30, 2020

News Daily News

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

Todd Neale

January 13, 2020

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 Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Class I Recall for 350,000 Medtronic Defibrillators: FDA

A Simple Nudge Moves the Needle on Statin Prescribing

FDA, Abbott Warn of Potential MitraClip Locking Malfunctions

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

DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

Cardiologs Unveils New Solution to Enable Use of Smartwatches for Remote Patient Monitoring

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

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

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

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

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

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

ACC, EHRA Cancel 2020 Meetings Over COVID-19

European Regulators Approve First Transcatheter MV Replacement Device

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

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

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

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