FDAJune 29, 2023device

Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323

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

The hazard

A higher than expected rate of thrombus formation or deposition has been observed. The risk is for thrombus formations or deposits on indwelling central venous lines or cannulas may break free and enter into the Impella RP Flex, resulting in reduced flow, loss of support, or hemolysis

What to do

FDA enforcement status: Ongoing

Brands named

abiomed

UPCs

00813502012811

Recall history

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

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Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323 — Recall Details · AllClear