International safety notice
Corrective action for Proteus XR/a X-ray imaging systems, GE Healthcare
Germany / BfArM · DEU · Mar 3, 2015
Key facts
| Title | Corrective action for Proteus XR/a X-ray imaging systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Proteus XR/a X-ray imaging systems, GE Healthcare |
| Manufacturer | Corrective action for Proteus XR/a X-ray imaging systems, GE Healthcare |
| Models | 53226, 2260354, 17108, 2273022-100 |
| Date | Mar 3, 2015 |
| 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