FDAJune 14, 2023device

Impella CP intravascular micro axial blood pump, Product Number 0048-0032

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

abiomed

UPCs

00813502011388

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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