FDAJanuary 27, 2026device

Impella RP with SmartAssist. Product Code: 0046-0035.

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

The hazard

Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.

What to do

FDA enforcement status: Ongoing

Brands named

abiomed

UPCs

00813502011869

Recall history

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

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