FDAOctober 4, 2023device

Acumen IQ Sensor with VAMP System, REFs: AIQS6AZ & AIQS6AZ5, STERILEEO, Rx only. For use in intravascular pressure monitoring.

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

The hazard

Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.

What to do

FDA enforcement status: Ongoing

Brands named

edwards lifesciencesedwards

UPCs

0069010320110900690103200980

Recall history

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

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