Product Wiki · Recalls · Health Canada — Medical Devices

COBAS IT MIDDLEWARE (2016-08-18) — recall 44352

Health Canada — Medical Devices · Canada · 2016-08-26 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
44352
Date of alert
2016-08-26
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: During the investigation of an issue from a customer complaint, it was found by the manufacturer that the daily cleanup sample can fail in deleting samples which are older than the configured retention period in the cobas IT middleware. Some samples which have been ordered from the lis and remain with open tests may not be deleted. Open tests are those for which results did not complete the processing cycle, including transmission to lis.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cobas-it-middleware-2016-08-18

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