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 recalls76since 2016
Last 12 months9reported
Class I6282% of total
Ongoing56latest 8 Apr 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 62 82%Class II 14 18%Class III 0 0%
Why philips respironics is recalled
Product types
By year
Ongoing philips respironics recalls
56 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Trilogy Evo recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy EV300 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo Universal recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo O2 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo O2 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
All philips respironics recalls, newest first
76 totalAbout 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.