International safety notice
Potential of wrong patient images when reviewing images on LOGIQ S8 Ultrasound System, GE Healthcare
Germany / BfArM · DEU · Feb 14, 2012
Key facts
| Title | Potential of wrong patient images when reviewing images on LOGIQ S8 Ultrasound System, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Potential of wrong patient images when reviewing images on LOGIQ S8 Ultrasound System, GE Healthcare |
| Manufacturer | Potential of wrong patient images when reviewing images on LOGIQ S8 Ultrasound System, GE Healthcare |
| Models | R1.1.0, 53226, 72285 |
| Date | Feb 14, 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