Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28108 |
| Brand Name: | Trilogy EVO |
| Model: | Trilogy Evo O2 devices with software versions 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01 and 1.06.02 |
| Affected: | |
| 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 identified two software issues related to pressure increase. The first issue is described as Infant/Pediatric EFS Calibration Pressure Increase and the second issue is described as Pressure Drift (Continuous Usage). |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/7/2021 |
