International safety notice
Potential therapy failure of Sigma pacemakers from Medtronic
Germany / BfArM · DEU · Dec 22, 2005
Key facts
| Title | Potential therapy failure of Sigma pacemakers from Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Potential therapy failure of Sigma pacemakers from Medtronic |
| Manufacturer | Potential therapy failure of Sigma pacemakers from Medtronic |
| Models | 17-38 |
| Date | Dec 22, 2005 |
| 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