FDAJune 26, 2018device

Monitor with one Blood Parameter Module and one HSat Probe; 500AHCT Monitor with two Blood Parameter modules and one HSat Probe; 500AVHCT Product Usage: The CDI System 500 provides continuous, on-line monitoring of the extracorporeal partial pressure of oxygen and carbon dioxide, pH, potassium, o...

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

The hazard

H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat population, which has resulted in an increase of Hybrids failing the H/Sat Color Chip Test which is an automated self-test when the device is powered on. This will not result in device inaccuracy, only Color Chip Test Failure which disables the H/Sat module.

What to do

FDA enforcement status: Terminated

Brands named

terumo cardiovascular systemsterumoterumo cardiovascular

Recall history

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

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