Product Wiki · Recalls · Health Canada — Medical Devices

Artis Zee Multi-Purpose, Artis Q (2019-04-22) — recall 59152

Health Canada — Medical Devices · Canada · 2019-05-24 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
59152
Date of alert
2019-05-24
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Siemens is providing a SW update VD11D patch 4 to equalize the SW in the field and reduce the number of SW-versions within the installed base. The new SW also provides a change in regards to the GRA board firmware and fixes the issue of corrupted images in Plane b.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/artis-zee-multi-purpose-artis-

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