International safety notice
" Ingenuity Flex, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Brilliance iCT, Brilliance iCT SP,,, Brilliance Big Bore Oncology, Brilliance Big Bore Radiology, Brilliance 16, Brilliance 40, Brilliance,, 64, IQon, Brilliance 6, Brilliance 10"
Ireland / HPRA · IRL · Apr 5, 2018
Key facts
| Title | " Ingenuity Flex, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Brilliance iCT, Brilliance iCT SP,, , Brilliance Big Bore Oncology, Brilliance Big Bore Radiology, Brilliance 16, Brilliance 40, Brilliance, , 64, IQon, Brilliance 6, Brilliance 10" |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | " Ingenuity Flex, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Brilliance iCT, Brilliance iCT SP, Brilliance Big Bore Oncology, Brilliance Big Bore Radiology, Brilliance 16, Brilliance 40, Brilliance 64, IQon, Brilliance 6, Brilliance 10" |
| Manufacturer | Philips Medical Systems |
| Models | 30205, 30263, 40106, 83570, 40083, 91096, 83312, 931001, 30237, 83515, 30214, 83317 and 237 more |
| Event type | Safety Notice |
| Date | Apr 5, 2018 |
| Regulator page | hpra.ie |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1