Product Wiki · Recalls · Health Canada — Medical Devices

Oxylog 3000 (2018-07-24) — recall 58358

Health Canada — Medical Devices · Canada · 2018-09-07 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58358
Date of alert
2018-09-07
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: A new software is now available with immediate effect for the Oxylog 3000. The new SW version 1.24 resolves a programming defect in the currently available SW version 1.23; The error resulted in the following three user advisory messages no longer being reported: 21 % by vol. Oxygen Self-test O.K. Setting not confirmed The new SW version 1.24 ensures that all user advisory messages are correctly displayed again. Other Oxylog ventilators, including the Oxylog 3000 plus, do not show this defective response.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/oxylog-3000-2018-07-24

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