International safety notice
Recall for the Columbus Revision knee endoprosthesis, Aesculap AG
Germany / BfArM · DEU · Feb 27, 2012
Key facts
| Title | Recall for the Columbus Revision knee endoprosthesis, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Columbus Revision knee endoprosthesis, Aesculap AG |
| Manufacturer | Recall for the Columbus Revision knee endoprosthesis, Aesculap AG |
| Models | NR072K, 78532, NR074K, 7461-95, NR076K, 18532, NR073K, D-78501, 14.02.2012, NR079K, 65109852, NR068K and 10 more |
| Date | Feb 27, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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