medical Class I Updated 2024-11-20

Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator. Model Number DS2000X11B.

Recalled Product

Trilogy Evo Universal Ventilator. Model Number DS2000X11B. 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

Distribution: Nationwide (United States)
Lot/Code Info: Model Number DS2000X11B, UDI-DI Number: 606959052000. All Serial Numbers.
View official government recall

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