International safety notice
Philips Allura Xper and Azurion Systems
Ireland / HPRA · IRL · Jul 5, 2023
Key facts
| Title | Philips Allura Xper and Azurion Systems |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Philips Allura Xper and Azurion Systems |
| Manufacturer | Philips Medical Systems Nederland BV |
| Models | 452300121801, 452300121851, 452220412801, 452220412741, 452300122031, 452300122051, 21821, 452300121971, 459800772263, 459800415571, 452220412761, 452300122021 and 80 more |
| Event type | Safety Notice |
| Date | Jul 5, 2023 |
| Regulator page | hpra.ie |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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