International safety notice
Revised Safety Notice for the product NordiPen®, Novo Nordisk
Germany / BfArM · DEU · Sep 10, 2013
Key facts
| Title | Revised Safety Notice for the product NordiPen®, Novo Nordisk |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product NordiPen®, Novo Nordisk |
| Manufacturer | Revised Safety Notice for the product NordiPen®, Novo Nordisk |
| Models | 903-264, DK-2880, 06131, 903-1875 |
| Date | Sep 10, 2013 |
| 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