Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25788 |
| Brand Name: | Expression Series Patient Monitors |
| Model: | |
| Affected: | Software Revisions: 01.03.00, 01.04.00, 01.05.00 and 01.07.00 |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Invivo, a division of Philips Medical Systems |
| Issue: | For MR400 devices with software revisions 01.03.00, 01.04.00, 01.05.00 and 01.07.00, the menu selections for users to access the O2 sensor calibration were changed. These changes were not incorporated into the device's Instructions for Use. As a result, the instructions for performing the O2 sensor calibration are incorrect for customers performing this task with an MR400 device with these software revisions. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 6/3/2020 |
