Philips Azurion And Allura Systems
Philips Medical Systems is recalling Azurion and Allura Systems in New Zealand. These are medical imaging devices used in hospitals and laboratories that need to be modified. This is classified as a Class I recall, which indicates a serious issue.
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Philips Azurion and Allura Systems. [Device]. Model: Allura Xper FD20, Azurion 7 B20, Azurion 7 M12, Azurion 7 M20
- Reason
- The manufacturer has identified that Hard Disk Drives HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Problems with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-05-12
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/ca9fc4b5-989c-44b3-a572-5d79d1e49fd5