International safety notice
Philips
United Kingdom / MHRA · GBR · Jun 24, 2019
Key facts
| Title | Philips |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Ingenuity CT, Ingenuity Core, Ingenuity Core 128, Brilliance 64, iCT, iCT SP, IQon, Ingenuity TF PET/CT, Vereos PET/CT |
| Manufacturer | Philips |
| Models | 88200522, 72800720, 728326, 728321 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Jun 24, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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