Devices

Allura Xper R8.2 and UNIQ R1.0 X-Ray Systems (diagnostic, fluoroscopic x-ray system)

Model / Serial
Allura Xper R8.2 and UNIQ R1.0 X-Ray Systems (diagnostic, fluoroscopic x-ray system)All Allura Xper R8.2 systems are affected and the following have been identified in Australia:Allura Xper FD10, 722026Allura Xper FD10/10, 722027Allura Xper FD20, 722028Allura Xper FD20 OR Table, 722035Allura Xper FD20/20 biplane OR Table, 722039Allura Xper FD20/15, 722058ARTG Number: 175708
Product Classification
Radiology Devices
Manufacturer
Philips Electronics Australia Ltd
1 Event
- Recall of Allura Xper R8.2 and UNIQ R1.0 X-Ray Systems (diagnostic, fluoroscopic x-ray system)

Manufacturer

Philips Electronics Australia Ltd

Manufacturer Parent Company (2017)
Philips
Source
DHTGA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)