Artis Q (2019-04-04)

Starting date:

April 4, 2019

Posting date:

April 29, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69748

Last updated: 2019-04-30

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  Reason
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  Affected products

Affected Products

Artis Q

Reason

Siemens is informing users of Artis systems equipped with a certain motor control unit, about a software error delivered starting May 2018. In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement. Usually activation of a collision sensor blocks all system movement but the floating tabletop, which is still possible to move. However, in the affected Artis systems movement of the floating tabletop is blocked as well.

Affected products