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Health Canada Medical devices

Philips Allura XPER, Allura Centron and Azurion Systems

Issued January 19, 2024
Issue
Philips has become aware of issues with three (3) components in certain PCs used with the Philips Allura XPER, Allura Centron and/or Azurion systems that may result in a loss of system functionality. Three (3) components of the PCs may not perform as intended due to manufacturing issues. The PCs within your system may have one (or more) of the impacted components. 1. Dimms (dual in-line memory modules): system may stop functioning and imaging may not be possible. 2. Disk bay: System may stop functioning and imaging may not be possible (eg. unresponsive, frozen images). 3. Framegrabber card: Flexvision monitor may show no viewports, or one or more viewports may show no image, a distorted image, or a frozen image. also, switching between viewports on the flexvision monitor may be possible. Recall start date: January 5, 2024
Hazard description
Performance
Product
Product name
Philips Allura XPER, Allura Centron and Azurion Systems
Reference
ID
RA-74931