International safety notice
Common name: Mobile digital general-purpose integrated X-ray fluoroscopic diagnostic equipment Brand name: (1) X-ray fluoroscopy diagnostic device CoreVision 3D (2) X-ray fluoroscopy diagnostic device CoreVision SD (3) X-ray fluoroscopy diagnostic device CoreVision LD
Japan / PMDA Recalls · JPN · May 30, 2024
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Mobile digital general-purpose integrated X-ray fluoroscopic diagnostic equipment Brand name: (1) X-ray fluoroscopy diagnostic device CoreVision 3D (2) X-ray fluoroscopy diagnostic device CoreVision SD (3) X-ray fluoroscopy diagnostic device CoreVision LD |
| Manufacturer | Fujifilm Co., Ltd. |
| Models | 28092, 58054, 28075, 58063, 58050, 58060, 28077, 28087, 58053, 58045, 58007, 28088 and 28 more |
| Date | May 30, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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