FDASeptember 4, 2019device

lmpella CP with Smart Assist, Model Number: 0048-0003. Left heart support blood pump, for Use During Cardiogenic Shock and High-Risk PCI

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

The hazard

This one pump shipped with incorrect pump programming, the initial production working version of the program. The pump would have immediately run at P9 for all selected P-levels, rather than a 10 second ramp up period. The pump may have migrated out of position and possibly caused injury. The positioning and suction alarms were also disabled.

What to do

FDA enforcement status: Terminated

Brands named

abiomed

UPCs

00813502011371

Recall history

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

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lmpella CP with Smart Assist, Model Number: 0048-0003. Left heart support blood pump, for Use During Cardiogenic Shock and High-Risk PCI — Recall Details · AllClear