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Digital Diagnost (2015-07-30)
- Starting date:
- July 30, 2015
- Posting date:
- August 18, 2015
- 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-54704
Affected Products
A. Digital Diagnost
Reason
Philips has become aware that the installed x-ray warning label at the Digital Diagnost with software release 4.0.x/4.1.x (EECA) is not in accordance with the local Canadian regulations.
Affected products
A. Digital Diagnost
Lot or serial number
>10, contact mfg.
Model or catalog number
9890 010 83904
Companies
- Manufacturer
-
Philips Medical Systems Dmc Gmbh
Rontgenstrabe 24
Hamburg
22335
GERMANY