Philips Respironics, Inc.

Frequent Recalls

8

Recalls

0

Units Recalled

0

Injuries

0

Deaths

1 category · 2026-04-01 to 2026-04-08

Date	Source	Product	Brand	Severity	Units
2026-04-08	FDA Device	FDA Recall: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi	Philips Respironics, Inc.	Class I	N/A
2026-04-08	FDA Device	FDA Recall: Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilat	Philips Respironics, Inc.	Class I	N/A
2026-04-08	FDA Device	FDA Recall: Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator devic	Philips Respironics, Inc.	Class I	N/A
2026-04-08	FDA Device	FDA Recall: Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.	Philips Respironics, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.	Philips Respironics, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilat	Philips Respironics, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator devic	Philips Respironics, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi	Philips Respironics, Inc.	Class I	N/A

Philips Respironics, Inc. Recalls | WatchRecall