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Interface De Resultats Sortants XML
- Starting date:
- March 29, 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-63126
Reason
A client reported a problem with sending requests to an outgoing results interface informed by XML format Omnitech interface files owing to the presence of a number of alternative identifiers for a single patient (i.e., ID #1, which was the file number for most patients). The duplicate identifiers are related to the deactivation of a patient identifier in the client's ADT system in the Omni-Lab patient information field or the Omni-Lab grouping module.
Affected products
Interface De Resultats Sortants XML
Lot or serial number
Not Applicable
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