Artis Zee Multi-Purpose and Artis Q (2019-04-22)

Starting date:

April 22, 2019

Posting date:

May 17, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69950

Last updated: 2019-05-17

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  Reason
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  Affected products

Affected Products

A. Artis Zee Multi-Purpose

B. Artis Q

Reason

Siemens is providing a SW update VD11E patch 5 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.

Affected products