Manufacturer Correction: Philips Respironics

About the Recall

Medical Device correction, for Trilogy Evo 02, Trilogy Evo Universal, Trilogy EV300, and Trilogy Evo ventilators

Affected Products:

Model: DS2000X118
Description:Trilogy Evo Universal Ventilator
UDI:606959052000

Model:DS2100X11B
Description:Trilogy Evo, 02, USA
UDI:606959051997

Model:DS2110X11B
Description:Trilogy Evo, USA
UDI:606959051942

Model:DS2200X11B
Description:Trilogy Evo, 02, USA EV300
UDI:606959052017

Model:IN2100X15B
Description:Trilogy Evo, 02, International
UDI:606959054059

Model:IN2110X15B
Description:Trilogy Evo, International
UDI:606959051959

Model:IN2200X15B
Description:Trilogy Evo, 02, INTL EV300
UDI:606959056497

Manufacturer Notice/Web Site:

medical-device-correction-philips-respironics-2023-CC-SRC-003-us.pdf

Actions to be taken by customer/Patient:

Contact your home medical equipment provider to arrange for a service technician to complete the necessary mitigation actions for your device.

You may also contact Philips Respironics Customer Service directly at 800-345-6443.