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Class I Recall for 350,000 Medtronic Defibrillators: FDA

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Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

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FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

Yael L. Maxwell

April 12, 2021

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

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FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

March 15, 2019

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