medical Class I Updated 2023-07-26

Abiomed, Inc. recalls Impella CP with SmartAssist intravascular micro axial blood

Recalled Product

Impella CP with SmartAssist intravascular micro axial blood pump, Product Numbers 0048-0024, 0048-0045, 1000080


Hazard / Issue

There is a potential risk for unintentional interaction of the Impella motor housing with the distal stent of a transcatheter aortic valve replacement (TAVR) resulting in destruction of the impeller blades. This has resulted in low flow from the damaged Impella system. Systemic embolization of the fractured impeller material is a possibility.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00813502011371, 00813502011876, 00813502012279;
View official government recall

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