International safety notice
Recall of SynchroMed II Implantable Infusion Pump Models 8637-20 and 8637-40, Medtronic
Germany / BfArM · DEU · Mar 1, 2016
Key facts
| Title | Recall of SynchroMed II Implantable Infusion Pump Models 8637-20 and 8637-40, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of SynchroMed II Implantable Infusion Pump Models 8637-20 and 8637-40, Medtronic |
| Manufacturer | Recall of SynchroMed II Implantable Infusion Pump Models 8637-20 and 8637-40, Medtronic |
| Models | FA574, 8637-20, 8637-40, FA553, FA696 |
| Date | Mar 1, 2016 |
| 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