Philips Respironics, Inc. recalls Aeris EVO. Model Number: VT2110X24B. Intended for invasive
Recalled Product
Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Hazard / Issue
Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.
Issued by
FDA
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