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Allura XPER FD10 (2015-01-29)
- Starting date:
- January 29, 2015
- Posting date:
- February 16, 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-43731
Recalled Products
A) Allura XPER FD10
Reason
Philips has received a customer feedback where the monitor ceiling suspension system fell to its lowest position. In this specific occasion it collided with the table top. The investigation initiated concluded that the cause of the failure was an assembly error of the actuator of the MCS.
Affected products
A) Allura XPER FD10
Lot or serial number
All lots.
Model or catalog number
ALLURA XPER FD10
Companies
- Manufacturer
-
Philips Medical Systems Nederland B.V.
Veenpluis 4-6
Best
5684 PC
NETHERLANDS