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Philips Respironics recalls - full list & free alerts

9 official U.S. recalls involving Philips Respironics in the last 12 months, most recently on 2026-04-08.

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Full list (9)

Philips Respironics, Inc.: Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-08 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-08 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-08 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-08 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-01 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-01 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-01 · Class I
Philips Respironics, Inc.: Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Medical DevicesFDA (device) · 2026-04-01 · Class I
Philips Respironics, Inc.: SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: Si
Medical DevicesFDA (device) · 2025-11-19 · Class II