International safety notice
Philips Medical Systems
United Kingdom / MHRA · GBR · Feb 8, 2018
Key facts
| Title | Philips Medical Systems |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Ingenuity Flex, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Brilliance iCT, Brilliance iCT SP, Brilliance Big Bore (Oncology), Brilliance Big Bore (Radiology), Brilliance 16 Slice (Air), Brilliance 16 Slice (Power), Brilliance 40, Brilliance 64, IQon Spectral CT, Brilliance 6 Slice (Air), Brilliance 10 Slice (Air), Brilliance CT Private Practice CV config |
| Manufacturer | Philips Medical Systems |
| Models | 728306, 728243, 728324, 728241, 728325, 728256, 728311, 728240, 728323, 728321, 728317, 728244 and 6 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Feb 8, 2018 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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