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Compass System - Main Software Application (2015-01-28)
- Starting date:
- January 28, 2015
- Posting date:
- March 20, 2015
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-52591
Recalled products
- Compass System - Main Software Application (2015-01-28)
Reason
During internal investigations related to Compass 3.1 and 3.1A it was found that dose reconstruction for DMLC plans from monaco or Eclipse-11 specifically when the jaws move or MLC leaves reverse during beam on was not scaled correctly.
Affected products
A. Compass System - Main Software Application (2015-01-28)
Lot or serial number
- software version 3.1a
Model or catalog number
- CS10-100
Companies
- Manufacturer
-
Siemens Ag
Wittelsbacherplatz 2
Muenchen
80333
GERMANY