International safety notice
General name: Whole-body X-ray CT diagnostic device Brand name: Incisive CT device
Japan / PMDA Recalls · JPN · Jun 5, 2023
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Whole-body X-ray CT diagnostic device Brand name: Incisive CT device |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 500472, 500314, 500461, 500476, 500333, 500409, 500241, 500375, 500470, 500487, 500328, 500488 and 1 more |
| Date | Jun 5, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No 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