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Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

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Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

October 29, 2021

FDA Investigating Possible Sex Differences in LAAO Outcomes

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FDA Investigating Possible Sex Differences in LAAO Outcomes

September 27, 2021

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

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FDA: Class I Recall of Precise PRO Rx Carotid Stent System

April 23, 2021

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