International safety notice
Urgent field safety notice for Vivid E95/E90/E80 with software version 201, revision 54.0 and 61.0. / Vivid S70/S60 with software version 201, revision 55.0 and 63.0. / Vivid S70N/S60N with software version 201, revision 63.0., GE Healthcare
Germany / BfArM · DEU · Mar 30, 2017
Key facts
| Title | Urgent field safety notice for Vivid E95/E90/E80 with software version 201, revision 54.0 and 61.0. / Vivid S70/S60 with software version 201, revision 55.0 and 63.0. / Vivid S70N/S60N with software version 201, revision 63.0., GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Vivid E95/E90/E80 with software version 201, revision 54.0 and 61.0. / Vivid S70/S60 with software version 201, revision 55.0 and 63.0. / Vivid S70N/S60N with software version 201, revision 63.0., GE Healthcare |
| Manufacturer | Urgent field safety notice for Vivid E95/E90/E80 with software version 201, revision 54.0 and 61.0. / Vivid S70/S60 with software version 201, revision 55.0 and 63.0. / Vivid S70N/S60N with software version 201, revision 63.0., GE Healthcare |
| Models | 76164, 76168, 53188 |
| Date | Mar 30, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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