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YSIO MAX (2015-11-04)
- Starting date:
- November 4, 2015
- 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-55872
Affected Products
YSIO MAX
Reason
Siemens has received complaints regarding the 3D tube head of the Ysio System moving to the planned and programmed end position faster than expected and then stopping with an error code. A system reboot is then required. This issue is due to a software bug.
Affected products
YSIO MAX
Lot or serial number
24102
24141
24171
24210
Model or catalog number
10762470
Companies
- Manufacturer
-
Siemens AG
Wittelsbacherplatz 2
Muenchen
80333
GERMANY