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FDA Classifies HeartWare(TM) HVAD(TM) Systems Unexpected Power Source Switching as Class I Recall

June 04, 2018

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Voluntary Recall of Fetch™ 2 Aspiration Catheter

April 11, 2016

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Voluntary Recall of Chariot™ Guiding Sheath

December 09, 2015

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Vascular Solutions, Inc. Issues Recall of Langston® Dual Lumen Catheters

July 03, 2014

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Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

May 12, 2014

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Boston Scientific Announces Voluntary Recall of iCross™ Coronary Imaging Catheters

May 27, 2011

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