This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Syngo.Via
- Starting date:
- October 10, 2012
- Posting date:
- October 29, 2012
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public (GP), Healthcare Professionals, Hospitals
- Identification number:
- RA-15166
Recalled Products:
Syngo.Via
Reason
Siemens has identified a potential malfunction when using Syngo.Via version VA11A_HF02 and higher. This malfunction occurs only with static and wholebody nuclear medicine images. In this case it can happen that the orientation labels at the segment borders are in conflict with the view name in the image text which has been entered by the user.
Affected products
Syngo.Via
Lot or serial number
- 100775
- 100861
- 100999
- 101000
- 101075
- 101132
- 101142
- 101464
- 101471
- 101511
Model or catalog number
IVK 104 96 180
Companies
- Manufacturer
-
Siemens AG