⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Is Philips Respironics recalled?

Philips Respironics recalls - full list & free alerts

Official U.S. agency records list 9 recalls involving Philips Respironics in the last 12 months, most recently on 2026-04-08. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (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
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