International safety notice
Recall of the NE330R Columbus/E.Motion Femural Inserter Extractor from Aesculap
Germany / BfArM · DEU · Dec 21, 2004
Key facts
| Title | Recall of the NE330R Columbus/E.Motion Femural Inserter Extractor from Aesculap |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the NE330R Columbus/E.Motion Femural Inserter Extractor from Aesculap |
| Manufacturer | Recall of the NE330R Columbus/E.Motion Femural Inserter Extractor from Aesculap |
| Date | Dec 21, 2004 |
| 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