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Displaying 21 - 40 of 81
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Impella RP Mortality Rate No Longer a Concern, FDA Says
News Daily News

Impella RP Mortality Rate No Longer a Concern, FDA Says

Caitlin E. Cox
Caitlin E. Cox
December 05, 2022
A Simple Nudge Moves the Needle on Statin Prescribing
News Daily News

A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan
Michael O'Riordan
December 02, 2022
FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs
News Daily News

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

Michael O'Riordan
Michael O'Riordan
October 17, 2022
LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support
News Daily News

LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support

L.A. McKeown
L.A. McKeown
September 30, 2022
Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect
News Daily News

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

L.A. McKeown
L.A. McKeown
April 29, 2022
HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage
News Daily News

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

L.A. McKeown
L.A. McKeown
January 21, 2022
Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF
News Conference News AHA 2021

Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF

Michael O'Riordan
Michael O'Riordan
November 19, 2021
FDA Investigating Possible Sex Differences in LAAO Outcomes
News Daily News

FDA Investigating Possible Sex Differences in LAAO Outcomes

Todd Neale
Todd Neale
September 27, 2021
Uptick in ‘Implausible’ Cancers Reported After ARB Recalls
News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown
L.A. McKeown
August 20, 2021
News Industry News

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

July 21, 2021
FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD
News Daily News

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

L.A. McKeown
L.A. McKeown
June 03, 2021
FDA: Class I Recall of Precise PRO Rx Carotid Stent System
News Daily News

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

Caitlin E. Cox
Caitlin E. Cox
April 23, 2021
FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds
News Daily News

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

Yael L. Maxwell
Yael L. Maxwell
April 12, 2021
FDA: Class I Recall for HeartWare VAD Pump Implant Kit
News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood
Shelley Wood
March 01, 2021
FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures
News Daily News

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

Michael O'Riordan
Michael O'Riordan
February 12, 2021
Lotus Edge TAVR Device Recalled and Discontinued Worldwide
News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan
Michael O'Riordan
November 18, 2020
CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair
News Daily News

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale
Todd Neale
July 01, 2020
 Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies
News Features

Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies

Shelley Wood
Shelley Wood
May 20, 2020
Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts
News Daily News

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

Shelley Wood
Shelley Wood
May 06, 2020
News Conference News

ACC, EHRA Cancel 2020 Meetings Over COVID-19

Michael O'Riordan
Michael O'Riordan
March 09, 2020

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