Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36575 |
| Brand Name: | Trilogy EVO |
| Model: | Trilogy Evo, Trilogy Evo O2 |
| Affected: | Update to latest software version 1.06.15.00. |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Respironics Inc |
| Brand Name: | Trilogy EV300 |
| Model: | Trilogy EV300 |
| Affected: | Update to latest software version 1.06.15.00. |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Respironics Inc |
| Issue: | The manufacturer has become aware of a potential problem when using in-line nebulisers in certain configurations with Trilogy Evo, Trilogy Evo O2, and Trilogy EV300 devices. The use of in-line nebulisers placed in certain locations can result in aerosol deposits accumulating over time on the device's internal flow sensor. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/2/2026 |





