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Displaying 21 - 28 of 28
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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 for CentriMag Circulatory Support System Motor
News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox
Caitlin E. Cox
November 07, 2019
New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure
News Daily News

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

Marcus A. Banks
Marcus A. Banks
July 24, 2019
FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting
News Daily News

FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

Todd Neale
Todd Neale
May 21, 2019
FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP
News Daily News

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

Caitlin E. Cox
Caitlin E. Cox
February 04, 2019
New Battery, Malfunction Issues Hit Beleaguered IABPs
News Daily News

New Battery, Malfunction Issues Hit Beleaguered IABPs

Todd Neale
Todd Neale
November 01, 2018
News Daily News

HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

Todd Neale
Todd Neale
May 23, 2018
News Daily News

FDA Classifies Latest HeartWare VAD Recalls as Class I

Michael O'Riordan
Michael O'Riordan
October 24, 2016

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