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FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

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FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

October 02, 2017

IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

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IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

September 06, 2017

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FDA: Class I Recall for Venture Catheters

June 21, 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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Abbott to Issue Urgent Recall of Certain Lots of Vascular Closure System

February 10, 2017

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FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

January 31, 2017

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Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’

January 11, 2017

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