Device recall
Z-1615-2026: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous…
FDA device recall · Class I · Philips Respironics, Inc.
Key facts
| Recall number (Z-number) | Z-1615-2026 |
|---|---|
| Recall event | 98537 |
| Product | Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device. |
| Product code | CBK |
| Recalling firm | Philips Respironics, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2518422 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database