International safety notice
Urgent Safety Notice for the Neurostimulation devices InterStim®, InterStim® II, Itrel®3 and Enterra®, Medtronic
Germany / BfArM · DEU · Jan 15, 2015
Key facts
| Title | Urgent Safety Notice for the Neurostimulation devices InterStim®, InterStim® II, Itrel®3 and Enterra®, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Neurostimulation devices InterStim®, InterStim® II, Itrel®3 and Enterra®, Medtronic |
| Manufacturer | Urgent Safety Notice for the Neurostimulation devices InterStim®, InterStim® II, Itrel®3 and Enterra®, Medtronic |
| Models | ITREL®3, FA639 |
| Date | Jan 15, 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