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FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

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FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

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FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

FDA Expands TAVR Indication to Low-Risk Patients

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FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

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FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

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FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

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FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

Michael O'Riordan

March 22, 2019

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

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FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

Michael O'Riordan

January 17, 2019

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