Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27305 |
| Brand Name: | EverFlo Oxygen Concentrator |
| Model: | All Philips EverFlo OPI |
| 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: | A problem has been identified with a limited number of Philips EverFlo OPI, Australia (PN 1020010) devices. Due to a manufacturing error, these devices may have been built with the incorrect power cord. As a result, these devices do not have required insulation on active and neutral pins of the plug. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/2/2021 |
