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FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

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FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

October 16, 2018

FDA Warns of Deaths, Stroke With Latest-Generation Total Artificial Heart

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FDA Warns of Deaths, Stroke Due to Power System Problems With Total Artificial Heart System

August 17, 2018

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

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FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

June 19, 2018

FDA: Clarithromycin Risks Persist in Patients With CAD

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FDA: Clarithromycin Risks Persist in Patients With CAD

February 26, 2018

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