International safety notice
Urgent Field Safety Notice for Vivid i, Vivid q, Vivid S., Vivid S. by GE Medical Systems Israel, Functional Imaging
Germany / BfArM · DEU · Jan 11, 2023
Key facts
| Title | Urgent Field Safety Notice for Vivid i, Vivid q, Vivid S., Vivid S. by GE Medical Systems Israel, Functional Imaging |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Vivid i, Vivid q, Vivid S., Vivid S. |
| Manufacturer | GE Medical Systems Israel, Functional Imaging |
| Models | FL092109, FN092039, FQ091013, FL092107, FQ092027, 18006825327, FQ092024, FQ092004, FN092087, 76194, FQ092018, FN092036 and 37 more |
| Date | Jan 11, 2023 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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