Uroskop Omnia & Uroskop Omnia Max (2020-09-11)

Recall Summary Uroskop Omnia and Uroskop Omnia Max medical devices are being recalled across Canada due to safety or effectiveness concerns. This Class I recall indicates a serious issue with the devices. The recall affects all Uroskop Omnia and Uroskop Omnia Max devices distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-10-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8ea0bee4-ede4-4fc4-8d58-83af10e3acb5