Devices

Brilliance iCT/iCT SP/Big Bore/6/10/16/16P/40/64 and Ingenuity CT/Core/Core128The following CT products manufactured from 1 January 2006 to 30 June 2014 are potentially affected:Brilliance iCT/Brilliance iCT SPBrilliance Big Bore Oncology/Brilliance Big Bore RadiologyBrilliance 6/Brilliance 10/Brilliance16/Brilliance 16P/Brilliance 40/Brilliance 64Ingenuity CT/Ingenuity Core/Ingenuity Core128

Model / Serial
Brilliance iCT/iCT SP/Big Bore/6/10/16/16P/40/64 and Ingenuity CT/Core/Core128The following CT products manufactured from 1 January 2006 to 30 June 2014 are potentially affected:Brilliance iCT/Brilliance iCT SPBrilliance Big Bore Oncology/Brilliance Big Bore RadiologyBrilliance 6/Brilliance 10/Brilliance16/Brilliance 16P/Brilliance 40/Brilliance 64Ingenuity CT/Ingenuity Core/Ingenuity Core128 ARTG Number: 98868
Manufacturer
Philips Electronics Australia Ltd
1 Event
- Recall of Brilliance iCT/iCT SP/Big Bore/6/10/16/16P/40/64 and Ingenuity CT/Core/Core128The following CT products manufactured from 1 January 2006 to 30 June 2014 are potentially affected:Brilliance iCT/Brilliance iCT SPBrilliance Big Bore Oncology/Brilliance Big Bore RadiologyBrilliance 6/Brilliance 10/Brilliance16/Brilliance 16P/Brilliance 40/Brilliance 64Ingenuity CT/Ingenuity Core/Ingenuity Core128

Manufacturer

Philips Electronics Australia Ltd

Manufacturer Parent Company (2017)
Philips
Source
DHTGA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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