FDADecember 16, 2014device

CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for human use, SENSATION and SENSATION PLUS IABC demonstration units. Part Number 0998-00-0800-xx; 0998-00-3023-xx; 0998-UC-0800-xx; 0998-UC-3023-xx An electromechanical system used to inflate and defl...

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

The hazard

Ferrule Cap was not removed on some fiber-optic Sensation and Sensation Plus IABC demonstration units. If fiber-optic connector is inserted into the Maquet CS300 or CARDIOSAVE IABP, cap will prevent connection of unit and may become dislodged and remain in IABPs fiber-optic receptacle.

What to do

FDA enforcement status: Terminated

Brands named

maquet datascope corp cardiac assist divisionmaquetmaquet datascope

Recall history

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

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