Philips Azurion Systems
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Philips Azurion systems. [Device]. Model: Module name: Azurion 7 M20. Affected: Product number: 722079
- Reason
- The manufacturer has identified that, in certain Azurion systems, one or more of these power supplies can fail due to energy peaks (surge voltages) during start or restart of the system. When a power supply failure occurs during a start or restart, the Power Distribution Unit does not provide the required direct current power to essential system components. As a result, the system does not successfully complete the (re-)start, imaging functionality is unavailable, and the system remains unavailable for clinical use.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-11-04
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/d41cdbcb-7432-440a-9d31-13e8c0c2ab23