International safety notice
General name: Extractor return type SPECT device for nuclear medicine diagnosis Sales name: (1) Emission CT device BRIGHTVIEW (2) Emission CT device BRIGHTVIEW X
Japan / PMDA Recalls · JPN · Jun 24, 2024
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Extractor return type SPECT device for nuclear medicine diagnosis Sales name: (1) Emission CT device BRIGHTVIEW (2) Emission CT device BRIGHTVIEW X |
| Manufacturer | Fujifilm Healthcare Co., Ltd. |
| Models | KPS0022801, KP10002001, KPS0059119, KPS0065101, KP10101201, KPS0093402, KPS0075204, KPS0063101, KPS0084302, KP10066101, KP10126201, KPS0081302 and 29 more |
| Date | Jun 24, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
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