Z-1614-2026

Class I · Ongoing

Recalling firm
Philips Respironics, Inc.
Classification
Class I
Status
Ongoing
Initiated
20260302
Firm location
Murrysville, PA, United States

Product description

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

Reason for recall

Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.

Data sourced from openFDA. This site is unofficial and independent of the FDA.