Official recall record
Selenia Dimensions 2D/3D Mammography Systems
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-06-10
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Hologic is initiating this voluntary field safety corrective action because the vertical travel assembly on 3Dimensions and Selenia Dimensions systems may experience internal bolt failure over time. The vertical travel assembly contains eight internal bolts that secure the c-arm to the assembly. Devices with loose, missing or broken bolts may exhibit shaking, vibration or uncommanded c-arm motion.
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 2026-06-21.
Record last checked against the registry on 2026-06-21.
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