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Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

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Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

August 17, 2023

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

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Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

Michael O'Riordan

August 10, 2023

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

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

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Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

March 31, 2023

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

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FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

February 27, 2023

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

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New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

January 25, 2023

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