FDADecember 12, 2024device

Impella RP Flex with SmartAssist; Product Number: 1000323;

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

The hazard

Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR) alarm and loss of Central Venous (CV) Placement Signal, Pulmonary Artery (PA) Placement Signal & Pulmonary Artery Pulse Index (PAPi) metrics. Abiomed is reinforcing that there is a risk of potential interaction between the tip of guidewires, indwelling central venous lines or devices and inlet of the Impella pumps listed above during the insertion, manipulation, and removal of those devices. The interaction may result in optical sensor damage, temporary pump stop, or permanent pump stop.

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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