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Health product recall

OmniLab V.12.0 - Laboratory Information System

Starting date:: February 10, 2017
Posting date:: February 28, 2017
Type of communication:: Medical Device Recall
Subcategory:: Medical Device
Hazard classification:: Type II
Source of recall:: Health Canada
Issue:: Medical Devices
Audience:: General Public, Healthcare Professionals, Hospitals
Identification number:: RA-62420

Reason
Affected products

Reason

While investigating a problem reported by a client, the Omnitech Labs team discovered that a combination of configurations prevents microbiology cases with a status of "preliminary amendment" and "preliminary comment" from appearing on the lists of cases awaiting processing. In short, the problem affects clients whose systems are configured for the use of validation by a microbiologist and the "confirmation" button that is found on the "identification" tab.

Affected products