Official recall record

Radiography 7000 M

Health Canada — Medical Devices · 2026-10-01 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2026-10-01
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

Philips has become aware of a potential safety issue impacting the Radiography 7000 M system (Model 712010) where the drive function may fail immediately after an exposure, causing the system to remain stationary. The issue may occur with the Radiography 7000 M system immediately after an exposure, causing the drive function to fail and preventing repositioning of the system. The system may remain stationary instead of driving upon activation of the handlebar. The issue is intermittent and has been observed during routine mobile radiography use.

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 2026-10-12.

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