Omnilab V.12.0 - Laboratory Information System (2016-08-11)

Recall Summary OmniLab V.12.0, a laboratory information system software, has been recalled across Canada due to being classified as a medical device with safety concerns. The recall affects all users of this 2016 software version in Canada. No additional details about the specific safety issue are provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2894c0f9-f3d0-49e8-a022-fa537c9958f2