International safety notice
General name: (1)-(3) X-ray fluoroscopy diagnostic device for stand-alone type circulator Sales name: (1) Entegris Allura Flat Detector (2) Angiography X-ray diagnostic device Allura Centron (3) Angiography X-ray diagnostic device Azurion
Japan / PMDA Recalls · JPN · Jun 24, 2024
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: (1)-(3) X-ray fluoroscopy diagnostic device for stand-alone type circulator Sales name: (1) Entegris Allura Flat Detector (2) Angiography X-ray diagnostic device Allura Centron (3) Angiography X-ray diagnostic device Azurion |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 722068, 722028, 722226, 722228, 722029, 722008, 722013, 722015, 722221, 722012, 703357, 722010 and 23 more |
| Date | Jun 24, 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