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Lotus Edge TAVR Device Recalled and Discontinued Worldwide

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Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

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Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

May 06, 2020

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

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FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

May 01, 2020

News Daily News

FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

January 13, 2020

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