International safety notice
Corrective action for the product MR Surgical Suite Option, GE Healthcare
Germany / BfArM · DEU · Nov 12, 2015
Key facts
| Title | Corrective action for the product MR Surgical Suite Option, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product MR Surgical Suite Option, GE Healthcare |
| Manufacturer | Corrective action for the product MR Surgical Suite Option, GE Healthcare |
| Models | 53226, M8053SS, 60885, M8074SS, M0074SS |
| Date | Nov 12, 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