Official recall record
ViziShot 2 Flex
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-08-21
- Last updated (per notice)
- 2026-02-04
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Olympus is removing all unexpired ViziShot 2 Flex (19g) devices due to a potential patient safety issue. Customers should not use any of the affected devices listed in the medical device recall letter and should return any affected products. Olympus is also reinforcing existing warnings in the Instructions for Use (IFU).
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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