International safety notice
-Vivid E95/E90/E80 con versión de software 201, revisión 54.0 y 61.0. - Vivid S70/S60 con versión de software 201, revisión 55.0 y 63.0.
Spain / AEMPS · ESP · May 31, 2024
Key facts
| Title | -Vivid E95/E90/E80 con versión de software 201, revisión 54.0 y 61.0. - Vivid S70/S60 con versión de software 201, revisión 55.0 y 63.0. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | -Vivid E95/E90/E80 con versión de software 201, revisión 54.0 y 61.0. - Vivid S70/S60 con versión de software 201, revisión 55.0 y 63.0. |
| Manufacturer | - GE Medical Systems Israel Ltd., Israel (para Vivid S70/S60). -GE Vingmed Ultrasound AS, Noruega (para Vivid E95/E90/E80 - Vivid S70N/S60N). |
| Models | 35-37, 28023, RECALL.76200, 2024-282, 28022, 76200, 106593, 91.822.52.89, 61.0.VIVID |
| Event type | Safety Notice |
| Date | May 31, 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