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Health product recall

INTERFACE DE RESULTATS SORTANTS XML (2015-06-05)

Starting date:
June 5, 2015
Posting date:
June 26, 2015
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-53916

Recalled Product

A.INTERFACE DE RESULTATS SORTANTS XML
 

Reason

A client reports that the results interpretation tables were not sent through the interface with the DSQ (Dossier de santé du Québec). The patient reports are published with the interpretation tables in the Omni-Lab system; however, in the XML format data extraction that feeds the DSQ file and the interfaces that feed from that same XML file, these requests were potentially send to the interface engine without the interpretation tables. The "getbio testshierarchy" component, revision 3 and 4, is involved.

Affected products

A.INTERFACE DE RESULTATS SORTANTS XML

Lot or serial number

Version 1.0.0.7

Model or catalog number

Version 1.0.0.7

Companies
Manufacturer
Omnitech Labs Inc.
Suite 1305, 215 Boul. Du Seminaire Sud
SAINT-JEAN-SUR-RICHELIEU, Quebec
J3B 8W1
CANADA