BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for the E1-Tapered 10° Liner 32/39, Biomet

Product group Non-active implants - bone surgery
Reference 05201/12

Biomet: Recall of all lots of its E1-tapered 10° Liner 32/39 (E1-103239). In a few cases the affected product does not properly fit in the acetabular cup.

Recall for the E1-Tapered 10° Liner 32/39, Biomet , Download_VeroeffentlichtAm_EN PDF, 1MB, 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)