Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26120 |
| Brand Name: | Anaesthetic Gas Module |
| Model: | IntelliVue G7m Anesthesia Gas Module |
| 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: | Philips Medizin Systeme Boblingen GmbH |
| Issue: | The 866173 IntelliVue G7m Anesthesia Gas Module may experience an interruption of gas measurement as a result of a firmware issue. This firmware issue may cause the device to erroneously detect a premature failure of the pump (a key component of the device), even though the pump neither has reached its end of life nor is at risk for failure. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/6/2020 |
