International safety notice
Sistemas Philips Azurion y Allura Xper con software R1.x. Ver nombre completo y modelos afectados en nota de aviso de la empresa
Spain / AEMPS · ESP · Mar 28, 2022
Key facts
| Title | Sistemas Philips Azurion y Allura Xper con software R1.x. Ver nombre completo y modelos afectados en nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Philips Azurion y Allura Xper con software R1.x. Ver nombre completo y modelos afectados en nota de aviso de la empresa |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos |
| Models | 78060, 722078, 722067, 28022, FCO72200505, SOFTWARER1.X, 91.822.52.89, 722065, 2021-IGT-BST-030, 722064, 722079, 722066 and 5 more |
| Event type | Safety Notice |
| Date | Mar 28, 2022 |
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