FDAMay 28, 2025device

CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit

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

The hazard

Due to an error in assembly of the thermistor within some units, the affected probes will experience inaccuracy in measured shunt sensor temperature. Additionally, following changes in patient temperature without an in vivo recalibration, affected probes may experience inaccuracy in other measured parameters, including pCO2, pO2, pH, Potassium and calculated parameters, including BE, Bicarbonate, Arterial Oxygen Saturation, Delivered Oxygen, Area Under of the Curve of Delivered Oxygen, Oxygen Consumption, and Oxygen Extraction Ratio, which utilize temperature as an input. Inaccurate data may lead to inappropriate user response.

What to do

FDA enforcement status: Ongoing

Brands named

terumo cardiovascular systemsterumoterumo cardiovascular

UPCs

00886799001889

Recall history

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

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