FDAAugust 15, 2017device

EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1

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

The hazard

The CO/CO2 sensor cable harness may have lower electromagnetic shielding, which might have resulted in a non-compliance with the IEC 60601-1-2 standard. As a consequence of a lower electromagnetic shielding provided by the cable harness, the CO/CO2 sensor could have been influenced by high frequencies emitted by very close devices.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1 — Recall Details · AllClear