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
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
Artis Q
Lot or serial number
Not applicable.
Model or catalog number
10848280
10848281
Companies
- Manufacturer
-
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY