Product Wiki · Recalls · Health Canada — Medical Devices

OmniLab V.12.0 - Laboratory Information System — recall 56174

Health Canada — Medical Devices · Canada · 2017-02-28 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
56174
Date of alert
2017-02-28
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: While investigating a problem reported by a client, the Omnitech Labs team discovered that a combination of configurations prevents microbiology cases with a status of "preliminary amendment" and "preliminary comment" from appearing on the lists of cases awaiting processing. In short, the problem affects clients whose systems are configured for the use of validation by a microbiologist and the "confirmation" button that is found on the "identification" tab.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/omnilab-v120-laboratory-inform

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