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FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

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FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

July 27, 2023

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

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Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

June 05, 2023

SCAI Updates Position on Doing PCI Without Surgical Backup

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SCAI Updates Position on Doing PCI Without Surgical Backup

Michael O'Riordan

February 20, 2023

Impella RP Mortality Rate No Longer a Concern, FDA Says

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Impella RP Mortality Rate No Longer a Concern, FDA Says

December 05, 2022

FDA: Class I Recall for CentriMag Circulatory Support System Motor

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FDA: Class I Recall for CentriMag Circulatory Support System Motor

November 07, 2019

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ICD and Pacemaker Needs After Open Heart Surgery: Series Provides a Benchmark

October 21, 2016

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