Philips Allura Xper Fd Angiographic X-ray
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Philips Allura Xper FD Angiographic X-Ray. [Device]. Model: Philips Allura Xper R8.1.x and R8.2.x systems with FlexVision monitor
- Reason
- The manufacturer has identified a software issue that may cause the FlexVision software application to become unresponsive during clinical use. When this occurs, the FlexVision monitor may either:, � turn blank and no longer display live images or other information shown on the FlexVision monitor; or, � freeze on the last displayed screen and no longer update live images or other information shown on the FlexVision Monitor., A cold system restart is required to restore normal FlexVision display functionality.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-10-21
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/34a8f67f-2671-4838-a904-f6d14994d85a