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Digital Diagnost (2014-09-25)
- Starting date:
- September 25, 2014
- Posting date:
- October 14, 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-41795
Recalled Products
Digital Diagnost
Reason
Philips has become aware that in the M-cabinet Componentized X-ray Architecture (CXA) wall box, the protective earth wires to the enclosure are not dimensioned according to Canadian requirements CAN/CSA-C22.2 NO.0.4 "Bonding of Electrical Equipment Impedance Test".
Affected products
Digital Diagnost
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
9890 010 8390X
Companies
- Manufacturer
-
Philips Medical Systems DMC GmbH
Rontgenstrabe 24
Hamburg
22335
GERMANY