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Displaying 1 - 19 of 19
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FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems
News Daily News

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

Todd Neale
Todd Neale
August 06, 2025
Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA
News Daily News

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Yael L. Maxwell
Yael L. Maxwell
April 03, 2024
Asundexian’s Lack of Efficacy Sinks OCEANIC-AF
News Daily News

Asundexian’s Lack of Efficacy Sinks OCEANIC-AF

L.A. McKeown
L.A. McKeown
November 20, 2023
‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF
News Daily News

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

L.A. McKeown
L.A. McKeown
September 18, 2023
Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath
News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood
Shelley Wood
July 26, 2023
Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis
News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan
Michael O'Riordan
June 17, 2021
FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters
News Daily News

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

Shelley Wood
Shelley Wood
February 24, 2020
FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter
News Daily News

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

Michael O'Riordan
Michael O'Riordan
October 09, 2019
FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device
News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

Shelley Wood
Shelley Wood
July 02, 2019
Two Pediatric Cardiac Catheters Recalled for Defective Balloons
News Daily News

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

L.A. McKeown
L.A. McKeown
April 26, 2019
Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early
News Daily News

Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early

Todd Neale
Todd Neale
October 09, 2017
Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High
News Daily News

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

Todd Neale
Todd Neale
July 12, 2017
News Daily News

FDA: Class I Recall for Venture Catheters

L.A. McKeown
L.A. McKeown
June 21, 2017
News Daily News

Apixaban Recalled Following Complaints of Dose-Packaging Mismatch

Shelley Wood
Shelley Wood
June 13, 2017
News Daily News

Abbott Vascular Recalls Three Coronary Catheters Because of Possible Sheath Removal Problems

Todd Neale
Todd Neale
May 16, 2017
News Daily News

Vascular Solutions Recalls Twin-Pass Dual-Access Catheters

Michael O'Riordan
Michael O'Riordan
October 06, 2016
News Daily News

Vascular Solutions Retira los Catéteres Gemelos de Doble Vía

Michael O'Riordan
Michael O'Riordan
October 06, 2016
News Daily News

FDA: No More Chances for Embattled Coagulation Monitoring System

Todd Neale
Todd Neale
July 13, 2016
News Daily News

FDA: No Más Oportunidades para el Acosado Sistema para Monitorizar la Coagulación

Todd Neale
Todd Neale
July 13, 2016
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