International safety notice
Vivid S60, Vivid S70, Vivid S60N y Vivid S70N. Ver versiones afectadas en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jul 6, 2023
Key facts
| Title | Vivid S60, Vivid S70, Vivid S60N y Vivid S70N. Ver versiones afectadas en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Vivid S60, Vivid S70, Vivid S60N y Vivid S70N. Ver versiones afectadas en la nota de aviso de la empresa. |
| Manufacturer | GE Medical Systems Israel Ltd., Israel. (para Vivid S60, Vivid S70). GE Vingmed Ultrasound AS, Noruega. (para Vivid S60N, Vivid S70N) |
| Models | 35-37, 95330, 95331, 28023, S70N.VER, 28022, 91.822.52.89, RECALL.FMI76195, 2023-319, 76195 |
| Event type | Safety Notice |
| Date | Jul 6, 2023 |
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