Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19578 |
| Brand Name: | Philips IntelliVue Information Centre (PIIC) |
| Model: | 866023 Intellivue Info Center iX, 866117 PIIC Classc Upgrade and 866389 IntelliVue Info Center iX |
| Affected: | all versions |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medical Systems |
| Issue: | Calcualated leads, also referred to as reconstructed ECG leads viewed or printed at the Information Centre iX may misrepresent the ECG waveform in specific leads. Lead combinations that are affected: Lead 1 and Lead 111 are used to derive the aVL Lead (incorrectly derived) Lead 1 and Lead aVR are used to derive the aVL Lead (incorrecty derived)' Lead 111 and Lead aVF are used to derive Lead 11 (incorrecty derived) |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/12/2015 |
