International safety notice
Urgent Safety Notice for the SynchroMed® Implantable Infusion Pump, Medtronic
Germany / BfArM · DEU · Nov 14, 2012
Key facts
| Title | Urgent Safety Notice for the SynchroMed® Implantable Infusion Pump, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the SynchroMed® Implantable Infusion Pump, Medtronic |
| Manufacturer | Urgent Safety Notice for the SynchroMed® Implantable Infusion Pump, Medtronic |
| Models | FA553, 29-31, MA12510A012 |
| Date | Nov 14, 2012 |
| 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