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ViziShot 2 Flex — recall 77960

Health Canada — Medical Devices · Canada · 2026-02-04 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 77960
Date of alert: 2026-02-04
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: General and plastic surgery
Product type: Medical devices

Reported risk: 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).

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vizishot-2-flex

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ViziShot 2 Flex — recall 77960

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