FDAAugust 18, 2017device

Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when non-invasive indicators warrant such.

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

The hazard

Intermittent communication between the host system and the FlexCardio

What to do

FDA enforcement status: Terminated

Brands named

invivo

UPCs

4535642419014535642419114535644833214535644833319898031856019898031930191

Recall history

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

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