Philips Respironics, Inc. recalls
All Philips Respironics, Inc. recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (22).
22 recalls published between November 20, 2024 and April 8, 2026. 21 were FDA Class I, the most serious level.
- Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy EV300, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy Evo, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy EV300, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00… recall
- Philips Respironics Trilogy Evo, Software Version 1.05.15.00… recall
- SimplyGo Mini, Standard Battery Kit recall
- DreamStation Auto recall
- DreamStation Auto BiPAP. Non-Continuous Ventilator recall
- DreamStation Auto CPAP. Non-Continuous Ventilator recall
- BiPAP A40 Ventilator recall
- BiPAP A30 Ventilators recall
- BiPAP V30 Auto Ventilator recall
- LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and… recall
- Garbin Evo recall
- Aeris EVO. Model Number: VT2110X24B. Intended for invasive and… recall
- Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B… recall
- Trilogy Evo Universal Ventilator recall
- Trilogy Evo recall
- Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B… recall