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OmniLab V.12.0 - Laboratory Information System
- Starting date:
- March 23, 2017
- Posting date:
- May 2, 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-63106
Reason
A client reported that some reports were not being published. Omnitech found out on March 17th that the publishing of certain reports was not performed due to a stored procedure that failed between February 28th to March 17th, 2017.
Affected products
OmniLab V.12.0 - Laboratory Information System
Lot or serial number
Not Applicable
Model or catalog number
12.10.0.119
Companies
- Manufacturer
-
Omnitech Labs Inc.
Suite 1305, 215 Boul. Du Seminaire Sud
SAINT-JEAN-SUR-RICHELIEU, Quebec
J3B 8W1
CANADA