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Apixaban Recalled Following Complaints of Dose-Packaging Mismatch

June 13, 2017

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FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

March 24, 2017

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FDA Warns of Cybersecurity Holes in Certain Cardiac Devices and Monitoring System

Yael L. Maxwell

January 09, 2017

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