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ALLURA XPER FD10/10-MAIN UNIT
- Starting date:
- August 8, 2016
- Posting date:
- September 23, 2016
- 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-60344
Affected products
Reason
Philips has become aware of a failure with the image disk causing the entire image processing chain to be blocked due to a software design error. This causes image data to be lost, and eventually loss of live imaging functionality.
Affected products
ALLURA XPER FD10/10-MAIN UNIT
Lot or serial number
All lots.
Model or catalog number
ALLURA XPER FD10/10
ALLURA XPER FD20/10
ALLURA XPER FD10
ALLURA XPER FD20
Companies
- Manufacturer
-
Philips Medical Systems Nederland B.V.
Veenpluis 4-6
Best
5684
NETHERLANDS