International safety notice
Common name: Stationary digital cardiovascular X-ray fluoroscopic diagnostic equipment Brand name: Angiography X-ray diagnostic device Azurion
Japan / PMDA Recalls · JPN · Oct 12, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Stationary digital cardiovascular X-ray fluoroscopic diagnostic equipment Brand name: Angiography X-ray diagnostic device Azurion |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 722079, 722223, 722221, 722068, 722224, 722225, 722226, 722067 |
| Date | Oct 12, 2021 |
| 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