ProductGuru Recalls

Official recall record

Azurion 7 Systems (ref 82841)

Health Canada — Medical Devices · 2026-10-21 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2026-10-21
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Philips Azurion systems use solid-state drives (SSDs) in various PCs to store the operating system and image data and to support system functionality. Philips has identified that, during certain repair or service actions, SSDs that are not specified in the medical device file may have been installed. These SSDs may have different performance characteristics, which may include reduced reliability over time. When an SSD does not perform as intended, the symptoms depend on the PC in which the SSD is installed and the function being used. this may result in loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-10-31.

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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.