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FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

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FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

August 05, 2019

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

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Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

July 22, 2019

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

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FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

July 02, 2019

TCTMD’s Top 10 Most Popular Stories for April 2019

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TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 2019

FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

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FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

February 22, 2019

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