International safety notice
Sistemas Philips Azurion R2.1.x. Ver nombre completo y modelo de los productos afectados en la nota de aviso de la empresa
Spain / AEMPS · ESP · Oct 29, 2021
Key facts
| Title | Sistemas Philips Azurion R2.1.x. Ver nombre completo y modelo de los productos afectados en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Philips Azurion R2.1.x. Ver nombre completo y modelo de los productos afectados en la nota de aviso de la empresa |
| Manufacturer | Philips Medical Systems Nederland BN, Países Bajos. |
| Models | 722222, SOFTWARE2.1.X, R2.1.XVER, 722221, 722063, 91.822.52.89, 2021-IGT-BST-018_72200494, R2.1.X, 722068, FCO72200494, 28050, 722223 and 14 more |
| Event type | Safety Notice |
| Date | Oct 29, 2021 |
At a glance
- No Recall
- Yes Field safety notice
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