Product Wiki · Recalls · Health Canada — Medical Devices

Interface De Resultats Sortants XML — recall 56727

Health Canada — Medical Devices · Canada · 2017-05-02 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
56727
Date of alert
2017-05-02
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: 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.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/interface-resultats-sortants-x

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