International safety notice
General name: (1)-(5) Whole-body X-ray CT diagnostic device Sales name: (1) Brilliance CT (2) Brilliance CT Power series (3) Brilliance iCT (4) Ingenuity CT series (5) IQon Spectral CT
Japan / PMDA Recalls · JPN · Feb 25, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: (1)-(5) Whole-body X-ray CT diagnostic device Sales name: (1) Brilliance CT (2) Brilliance CT Power series (3) Brilliance iCT (4) Ingenuity CT series (5) IQon Spectral CT |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 100142, 860027, 300241, 860078, 333013, 95431, 100517, 860075, 860022, 300249, 333053, 200051 and 6 more |
| Date | Feb 25, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No 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