Philips Respironics recalls
Philips Respironics has 76 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 8 Apr 2026. 56 are still ongoing. 9 were reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls 76 since 2016
Last 12 months 9 reported
Class I 62 82% of total
Ongoing 56 latest 8 Apr 2026
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 62 82% Class II 14 18% Class III 0 0%
Why philips respironics is recalled
Ongoing philips respironics recalls 56 active
All philips respironics recalls, newest first 76 total
Reported Class Recall Company Reason Where 8 Apr 2026 Device CLASS I Trilogy Evo recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 8 Apr 2026 Device CLASS I Trilogy EV300 recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 8 Apr 2026 Device CLASS I Trilogy Evo Universal recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 8 Apr 2026 Device CLASS I Trilogy Evo O2 recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 1 Apr 2026 Device CLASS I Trilogy Evo recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 1 Apr 2026 Device CLASS I Trilogy Evo O2 recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 1 Apr 2026 Device CLASS I Trilogy EV300 recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 1 Apr 2026 Device CLASS I Trilogy Evo Universal recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 19 Nov 2025 Device CLASS II SimplyGo Mini, Standard Battery Kit recalled by Philips Respironics Philips Respironics Temperature Abuse Nationwide 20 Aug 2025 Device CLASS I DreamStation Auto CPAP recalled by Philips Respironics Philips Respironics Other Nationwide 20 Aug 2025 Device CLASS I DreamStation Auto recalled by Philips Respironics Philips Respironics Other Nationwide 20 Aug 2025 Device CLASS I DreamStation Auto BiPAP recalled by Philips Respironics Philips Respironics Other Nationwide 20 Nov 2024 Device CLASS I Trilogy Evo recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I Trilogy Evo O2 recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I LifeVent EVO2 recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I Garbin Evo recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I Aeris EVO recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I Trilogy EV300 recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 20 Nov 2024 Device CLASS I Trilogy Evo Universal Ventilator recalled by Philips Respironics Philips Respironics Labeling Errors Nationwide 24 Apr 2024 Device CLASS I Trilogy Evo, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I Garbin EVO, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I Trilogy EV300, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I Trilogy Evo O2, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I Aeris EVO, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I LifeVentEVO2, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 24 Apr 2024 Device CLASS I Trilogy Evo Universal Ventilator, all recalled by Philips Respironics Philips Respironics Device Malfunction Nationwide 10 Jan 2024 Device CLASS II Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B recalled Philips Respironics Other Nationwide 4 Oct 2023 Device CLASS I V60/V60 Plus Ventilator, PCBA recalled by Philips Respironics Philips Respironics Device Malfunction 4 states 12 Jul 2023 Device CLASS II Trilogy Evo, Evo Clinical Korean (1137823) recalled Philips Respironics Other PA 12 Apr 2023 Device CLASS I Philips DreamStation Auto BiPAP and CPAP recalled by Philips Respironics Philips Respironics Other Nationwide
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About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.