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EOS (2015-02-17)
- Starting date:
- February 17, 2015
- Posting date:
- April 13, 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-52855
Recalled Products
EOS
Reason
An alert message on the spectral filtration of the x-ray beam is possibly not managed appropriately at the time of its appearance during the daily calibration of the system.
Affected products
EOS
Lot or serial number
- 3.1009.127
- 3.1210.220
- 3.1303.231
- 3.1306.239
- 3.1310.255
- 5.1409.290
- 5.1410.300
Model or catalog number
EOS
Companies
- Manufacturer
-
EOS IMAGING
10, RUE MERCOEUR
PARIS, FRANCE
75011