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Allura Xper FD10 (2014-12-09)
- Starting date:
- December 9, 2014
- Posting date:
- December 23, 2014
- 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-42981
Recalled Products
Allura Xper FD10
Reason
Philips has become aware that a mechanical noise/tick might occur when moving the XY-carrier over the X-rail coupling. This problem can occur when an "old" version of coupling block with M5 bolts is installed in the system.
Affected products
Allura Xper FD10
Lot or serial number
All lots.
Model or catalog number
ALLURA XPER FD10
Companies
- Manufacturer
- Philips Medical Systems Nederland B.V.
