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OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM (2016-08-11)
- Starting date:
- August 11, 2016
- Posting date:
- August 26, 2016
- 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-60008
Affected Products
OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM
Reason
When OMNI Lab publishes a report by fax, if the electronic facsimile-transmission system (fax machine or third-party software) is not available or not responding, OMNI Lab will populate an error code ("pcl") after several unsuccessful attempts. The report will then have to be re-published by a user via OMNI Lab's publishing option or published manually by Omnitech Labs's team.
Affected products
OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM
Lot or serial number
Not applicable
Model or catalog number
Not applicable
Companies
- Manufacturer
-
Omnitech Labs Inc.
Suite 1305, 215 Boul. Du Seminaire Sud
SAINT-JEAN-SUR-RICHELIEU, Quebec
J3B 8W1
CANADA