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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

July 26, 2023

Penumbra’s JET 7 Recall: A Kick Start to Change?

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Penumbra’s JET 7 Recall: A Kick Start to Change?

December 01, 2021

TCTMD’s Top 10 Most Popular Stories for April 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

May 03, 2021

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

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Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

July 21, 2017

News Daily News

FDA: ROCKET AF Results Not Affected by Faulty INR Testing in Warfarin Arm

Michael O'Riordan

October 11, 2016

News Daily News

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

March 24, 2016

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ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

February 04, 2016

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

July 20, 2011

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