Omnilab V.12.0 - Laboratory Information System

OmniLab V.12.0 Laboratory Information System Recall OmniLab V.12.0, a laboratory information system, is being recalled across Canada due to issues classified as a Class I medical device concern. The recall affects users of this software system that is used in laboratory settings.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-05-02
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6001d61e-364c-4886-b46c-e08803a8cc89