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XVI 4.2.1, 4.5.1 and 4.5.0 (January 08, 2013)
- Starting date:
- January 8, 2013
- Posting date:
- February 18, 2013
- 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-23441
Reason
In some Treatment Planning System TPS, different Dicom RT structures with the same name show incorrectly in the Device XVI.
Affected products
XVI 4.2.1, 4.5.1 and 4.5.0 (2013-01-08)
Lot or serial number
FCO REF: 20001507069, FCO REF: 20001507071
Model or catalog number
MRT 13221, MRT 14921, MRT 14931, MRT 9451
Companies
- Manufacturer
-
Elekta Ltd.