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Health product recall

OMNI-Lab - Laboratory Information System (2014-06-16)

Starting date:
June 16, 2014
Posting date:
July 15, 2014
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-40509

Recalled Products

  1. OMNI-Lab - Laboratory Information System 

Reason

The result of an examination for parasites may be transferred to a microbiology requisition (culture). In other words, if a user selects a culture result for a parasitology requisition at the "identification" tab, then clicks in the "requisition number" field of the basic tab of the main screen of the microbiology module, and then enters a microbiology requisition number (or scans a requisition label using a barcode reader), the result of the parasitology requisition on the screen is in the microbiology requisition called to the screen. The microbiology requisition result is replaced with a parasitology result.

Affected products

A. OMNI-Lab - Laboratory Information System 

Lot or serial number
  • Version 12.10.0.129
  • Version 12.10.0.130
Model or catalog number

Not applicable

Companies
Manufacturer
Omnitech Labs Inc.
215, Boul. Du Seminaire Sud, Suite 1305
Saint-jean-sur-richelieu
J3B 8W1
Quebec
CANADA