Official recall record
Portable X-Ray Unit FDR Xair
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-03-05
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
The residual risk information of the XD2000 provided was not sufficient. There is the potential defectiveness for users to be exposed to unnecessary radiation by unintended handheld use. The users should understand the notification letter issued by FujiFilm and operate the XD2000 in accordance with the revised operation manual. Recall Start Date: February 26, 2025
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 2026-05-31.
Record last checked against the registry on 2026-05-31.
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