This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Omnilab Version 12 (2014-03-06)
- Starting date:
- March 6, 2014
- Posting date:
- April 4, 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-38661
Recalled products
- Omnilab Version 12
Reason
In the main "order entry" screen and in the "analyzing" screen of the core lab module, users can delete the priority for a test and leave the field empty, or press the spacebar to only insert a blank space.
Affected products
A. Omnilab Version 12
Lot or serial number
More than 10 numbers, contact manufacturer
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