Iom Luminos Drf System - Main Unit And Uroskop Omnia (2013-09-02)

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2013-10-16
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1c22ac43-5d54-42bd-b409-235fab113d90