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News Daily News

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

L.A. McKeown

July 12, 2023

News Daily News

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

L.A. McKeown

July 11, 2023

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

News Daily News

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

L.A. McKeown

December 06, 2022

News Daily News

Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

L.A. McKeown

April 26, 2022

News Daily News

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

L.A. McKeown

January 21, 2022

News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

L.A. McKeown

January 13, 2022

News Daily News

FDA Investigating Possible Sex Differences in LAAO Outcomes

Todd Neale

September 27, 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: Class I Recall for Cook Medical’s CrossCath Support Catheters

L.A. McKeown

December 17, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

News Daily News

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

L.A. McKeown

March 15, 2019

News Daily News

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

L.A. McKeown

February 19, 2019

News Daily News

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

Michael O'Riordan

November 06, 2018

News Daily News

INR Test Strips Recalled Due to Inaccurate Measurements

Todd Neale

November 02, 2018

News Daily News

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

Michael O'Riordan

January 17, 2018

News Daily News

FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts

Michael O'Riordan

August 17, 2017

News Daily News

Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High

Todd Neale

July 12, 2017

News Daily News

Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data

L.A. McKeown

December 13, 2016

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CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

FDA Safety Communication Updates Stance on Endologix AAA Grafts

FDA Investigating Possible Sex Differences in LAAO Outcomes

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

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

FDA Expands TAVR Indication to Low-Risk Patients

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

INR Test Strips Recalled Due to Inaccurate Measurements

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts

Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High

Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data

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