International safety notice
Software Update required for Innova 2121IQ and Innova 3131IQ X-ray systems, GE Healthcare
Germany / BfArM · DEU · Sep 3, 2012
Key facts
| Title | Software Update required for Innova 2121IQ and Innova 3131IQ X-ray systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Innova 2121IQ and Innova 3131IQ X-ray systems, GE Healthcare |
| Manufacturer | Software Update required for Innova 2121IQ and Innova 3131IQ X-ray systems, GE Healthcare |
| Models | 12184, 3131IQ, 53226, 2121IQ |
| Date | Sep 3, 2012 |
| 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