Product Wiki · Recalls · Health Canada — Medical Devices

Omnilab Advanced and BiPAP A40 — recall 64502

Health Canada — Medical Devices · Canada · 2022-08-31 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
64502
Date of alert
2022-08-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Anaesthesiology
Product type
Medical devices
Reported risk: As a result of a supplier notification, Philips determined that certain devices were built with motor assemblies that could contain non-conforming plastic material. If the non-conforming plastic is present in the device motor, it could lead to off-gassing that would not occur in a device within specification. The presence of non conforming plastic could lead to structural failure causing the immediate and sudden failure of the device during use. Recall start date: August 26, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/omnilab-advanced-and-bipap-a40

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