International safety notice
Sistemas Philips Azurion y Allura Xper instalados con la opción FlexMove. Ver modelos y códigos de productos afectados en el apéndice A de la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jun 30, 2023
Key facts
| Title | Sistemas Philips Azurion y Allura Xper instalados con la opción FlexMove. Ver modelos y códigos de productos afectados en el apéndice A de la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Philips Azurion y Allura Xper instalados con la opción FlexMove. Ver modelos y códigos de productos afectados en el apéndice A de la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos. |
| Models | 722012, 722023, 703365, 722035, 722026, 703922, 703529, 722028, 94667, 704146, 2023-304, 703918 and 24 more |
| Event type | Safety Notice |
| Date | Jun 30, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 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