BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of the Alpha Durasul Inlays from Zimmer

Product group Non-active implants
Reference 00268/07

Recall of certain lots of Alpha Durasul Inlays by Zimmer GmbH (see Advisory Notice) due to commingling of the products. This may cause either difficulties in impacting the inlay or impede stable fixation of the inlay.

Recall of the Alpha Durasul Inlays from Zimmer , Download_VeroeffentlichtAm_EN PDF, 31KB, 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