Uroskop Omnia, Uroskop Omnia Max (2019-02-07)

Recall Summary Uroskop Omnia and Uroskop Omnia Max medical devices are being recalled across Canada due to a safety or performance issue. This recall affects all users of these devices in Canada. The devices are classified as a Class I recall, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-02-22

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/36dc1d54-0ce2-4e5d-90a0-0b746853e981