HomeMedical Device recalls
High severity

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

SourceFDA Device Enforcement
CategoryMedical Device
SeverityHigh
Statusongoing
Recall dateMarch 02, 2026
ReportedApril 08, 2026
Recalling firmPhilips Respironics, Inc.
Country / regionUnited States PA

Hazard

In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.

Affected products

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