Product Wiki · Recalls · Health Canada — Medical Devices

OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM (2016-08-11) — recall 55993

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

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Agency
Health Canada — Medical Devices
Recall identifier
55993
Date of alert
2016-08-26
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: When OMNI Lab publishes a report by fax, if the electronic facsimile-transmission system (fax machine or third-party software) is not available or not responding, OMNI Lab will populate an error code ("pcl") after several unsuccessful attempts. The report will then have to be re-published by a user via OMNI Lab's publishing option or published manually by Omnitech Labs's team.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/omnilab-v120-laboratory-inform

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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