International safety notice
Urgent Safety Notice for Optima XR220amx, Optima XR200amx and Brivo XR285amx mobile X-ray systems, GE Healthcare
Germany / BfArM · DEU · Aug 30, 2012
Key facts
| Title | Urgent Safety Notice for Optima XR220amx, Optima XR200amx and Brivo XR285amx mobile X-ray systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Optima XR220amx, Optima XR200amx and Brivo XR285amx mobile X-ray systems, GE Healthcare |
| Manufacturer | Urgent Safety Notice for Optima XR220amx, Optima XR200amx and Brivo XR285amx mobile X-ray systems, GE Healthcare |
| Models | 5555000-2, 5555000-4, XR220AMX, XR285AMX, XR200AMX, 10866, 5555000-6, 53226, FMI10866_FSN_ENGLISH, 5555000-5, 5555000-3, 5555000 |
| Date | Aug 30, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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