International safety notice
Information for implantable neurostimulators, Model 7428 Kinetra and 7426 Soletra, Medtronic
Germany / BfArM · DEU · Nov 9, 2007
Key facts
| Title | Information for implantable neurostimulators, Model 7428 Kinetra and 7426 Soletra, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | implantable neurostimulators, Model 7428 Kinetra and 7426 Soletra, Medtronic |
| Manufacturer | Information for implantable neurostimulators, Model 7428 Kinetra and 7426 Soletra, Medtronic |
| Models | FA356 |
| Date | Nov 9, 2007 |
| 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