International safety notice
Sistema de fluoroscopiaAllura Xper FD10/FD20 con mesa del paciente AD7NT (sin inclinación). Ver productos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · May 28, 2024
Key facts
| Title | Sistema de fluoroscopiaAllura Xper FD10/FD20 con mesa del paciente AD7NT (sin inclinación). Ver productos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de fluoroscopiaAllura Xper FD10/FD20 con mesa del paciente AD7NT (sin inclinación). Ver productos afectados en la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos. |
| Models | 2024-IGT-BST-006, 722012, AD7NT, 91.822.52.89, 28022, 8.1.100, ADN7NT, SOFTWARE8.1.100, FCO72200588, 2024-270, 106203, 722013 and 2 more |
| Event type | Safety Notice |
| Date | May 28, 2024 |
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