Medtronic Recalls Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds) Due to Risk of Shortened Battery Life

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Medtronic Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds)

Models: Full List of Affected Devices below

Serial Numbers: Full List of Affected Devices below

Distribution Dates: August 31, 2012 to May 9, 2018

Devices Recalled in the U.S.: 239,171

Date Initiated by Firm: February 3, 2021

USA-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-evera-viva-brava-claria-amplia-compia-and-visia-implantable-cardioverter