Recall for the Columbus Revision knee endoprosthesis, Aesculap AG
2012.02.27
Product group Non-active implants - bone surgery
Reference 01001/12
The manufacturer Aesculap AG informs about the product recall of the Columbus Revision knee endoprosthesis due to dimensional deviations of the components.
Recall for the Columbus Revision knee endoprosthesis, Aesculap AG , Download_VeroeffentlichtAm_EN