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FDA: Class I Recall for CentriMag Circulatory Support System Motor

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FDA: Class I Recall for CentriMag Circulatory Support System Motor

November 07, 2019

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

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

February 04, 2019

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FDA Issues Class I Recall for Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits

Michael O'Riordan

March 18, 2016

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