Official recall record
VISERA™ Imaging System
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-10
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of MAJ-210 and MAJ-1218. Olympus is highlighting the importance of strictly adhering to the IFU. Olympus will share an updated customer notification by mid-2026.
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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