Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 17594 |
| Brand Name: | Philips IntelliVue Patient Monitors |
| Model: | Models: MP5 (M8105A), MP5SC (M8105AS), MP5T (M8105AT), MP5 Upgrades (M8105AU, 866327) |
| Affected: | |
| Software version: | Software revisions J.21.03, J.21.19 |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medizin Systeme Boblingen GmbH |
| Brand Name: | Philips Avalon Fetal Monitors |
| Model: | Models: FM20 (M2702A), FM30 (M2703A), FM50 (M2705A) |
| Affected: | |
| Software version: | Software revision J.30.58 |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medizin Systeme Boblingen GmbH |
| Issue: | In time-synchronized automatic/sequence mode, the non-invasive blood pressure (NBP) automatic measurement series is stopped inadvertently if the repetition interval is increased manually by the user (e.g. from 5 to 15 minutes) in between two consecutive measurements. If the NBP measurement is stopped, and a patient's blood pressure is not being monitored, a delay in treatment could occur. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/10/2014 |
