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Axiom Luminos DRF System-Main Unit (2014-08-12)
- Starting date:
- August 12, 2014
- Posting date:
- August 28, 2014
- 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-41209
Recalled products
- Axiom Luminos DRF System-Main Unit
Reason
There exist a potential of malfunction and hence hazard to patients and personnel when exposing the tableside control panel of the Luminos DRFsystem to fluids. In case of exposure to fluids, the tableside control panel may be infiltrated by fluids. As a result malfunctions of the tableside control panel may occur when buttons on the control panel are pressed.
Affected products
A. Axiom Luminos DRF System-Main Unit
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
- 10094200
Companies
- Manufacturer
-
Siemens AG
Wittelsbacherplatz 2
Muenchen, Germany
80333