BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall for the “Achsstielknie” prosthesis, AQ Implants GmbH

2012.09.11

Product group Non-active implants - bone surgery
Reference 05568/12

The manufacturer AQ Implants informs about a recall of several lots of the “Achsstielknie” prosthesis as the pre-assembly of the components may be incorrect. Advisory Notice is only available in German language.

Lot Recall for the “Achsstielknie” prosthesis, AQ Implants GmbH , Download_VeroeffentlichtAm_EN PDF, 58KB, File does not meet accessibility standards

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK