International safety notice
Allura Xper, Allura Centron y Azurion. Ver números de modelo afectados en el apéndice A de la nota de aviso de la empresa.
Spain / AEMPS · ESP · Feb 7, 2024
Key facts
| Title | Allura Xper, Allura Centron y Azurion. Ver números de modelo afectados en el apéndice A de la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Allura Xper, Allura Centron y Azurion. Ver números de modelo afectados en el apéndice A de la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Holanda. |
| Models | 722010, 722013, 722001, 722003, 540019920, 070000122, 510020523, 510999920, 722015, 2024-073, 722058, FD10C and 51 more |
| Event type | Safety Notice |
| Date | Feb 7, 2024 |
At a glance
- No Recall
- Yes 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