International safety notice
Recall for 1x4 Deep Brain Stimulation Extension Kit, Medtronic
Germany / BfArM · DEU · May 4, 2009
Key facts
| Title | Recall for 1x4 Deep Brain Stimulation Extension Kit, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | 1x4 Deep Brain Stimulation Extension Kit, Medtronic |
| Manufacturer | Recall for 1x4 Deep Brain Stimulation Extension Kit, Medtronic |
| Models | 37085, FA429 |
| Date | May 4, 2009 |
| 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