Medical device recalls High risk

GE Healthcare, LLC recalls Airway Gas Option N-CAiO

Recall date
September 27, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0760-2020
FDA classification
Class I
Brand / firm
GE Healthcare, LLC
Sold / distributed
US OUS: Australia, Austria, Belgium, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Czech Republic, Finland, France, Germany, Hong Kong, India, Indonesia, Ireland, Italy, Japan, Korea (Republic of), Malaysia, Mexico, Myanmar, Netherlands, New Zealand, Peru, Poland, Republic of Serbia,…

Why it was recalled

Displayed End Tidal Oxygen (EtO2) and Fraction of Inspired Oxygen (FiO2) values may be incorrect which could cause up to 50% measurement error in the EtO2/FiO2 values.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Airway Gas Option N-CAiO

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