International safety notice
Urgent Safety Notice/Corrective action for various GE Healthcare MRI systems, GE Healthcare
Germany / BfArM · DEU · Apr 20, 2015
Key facts
| Title | Urgent Safety Notice/Corrective action for various GE Healthcare MRI systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | various GE Healthcare MRI systems, GE Healthcare |
| Manufacturer | Urgent Safety Notice/Corrective action for various GE Healthcare MRI systems, GE Healthcare |
| Models | MR450W, 53226, MR360, MR355, MR750, MR450, 60878, MR950, MR750W |
| Date | Apr 20, 2015 |
| 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