International safety notice
Aplicación Sagittal VIBRANT con ASSET utilizada en determinados sistemas de resonancia magnética. Ver sistemas afectados con sus versiones de software en la nota de aviso de la empresa
Spain / AEMPS · ESP · Sep 28, 2021
Key facts
| Title | Aplicación Sagittal VIBRANT con ASSET utilizada en determinados sistemas de resonancia magnética. Ver sistemas afectados con sus versiones de software en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Aplicación Sagittal VIBRANT con ASSET utilizada en determinados sistemas de resonancia magnética. Ver sistemas afectados con sus versiones de software en la nota de aviso de la empresa |
| Manufacturer | GE Healthcare, EEUU. |
| Models | 00195278117021, RX27.3, 00840682115872, 28022, 00840682146104, SV29.1, MR750W, PX25.4, 00840682115971, 60982, 91.822.52.89, MR450W and 39 more |
| Event type | Safety Notice |
| Date | Sep 28, 2021 |
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