International safety notice
Urgent Field Safety Notice for O-ARM Imaging System by Medtronic Navigation Inc.
Germany / BfArM · DEU · Jan 16, 2020
Key facts
| Title | Urgent Field Safety Notice for O-ARM Imaging System by Medtronic Navigation Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | O-ARM Imaging System |
| Manufacturer | Medtronic Navigation Inc. |
| Models | C2181, C2227, C2262, C2182, C2226, C2207, C2239, C2222, C2220, C2252, C2263, C2218 and 81 more |
| Date | Jan 16, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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