International safety notice
General name: Whole-body X-ray CT diagnostic device Brand name: Whole body X-ray CT diagnostic device Supria
Japan / PMDA Recalls · JPN · Aug 16, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Whole-body X-ray CT diagnostic device Brand name: Whole body X-ray CT diagnostic device Supria |
| Manufacturer | Fujifilm Healthcare Co., Ltd. |
| Models | G1Z0152621, G1Z0310921, G1Z0026220, G1Z0017020, G1Z0077821, G1Z0136619, G120247220, G1Z0273921, G1Z0311521, G1Z0005220, G1Z0070320, G1Z0032722 and 391 more |
| Date | Aug 16, 2022 |
| 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