BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for the RHK knee system, Biomet

Product group Non-active implants - bone surgery
Reference 07959/12

The manufacturer Biomet informs about a recall of several catalogue numbers of RHK knee system as the items have possibly been manufactured with an oversized diameter axle.

Recall for the RHK knee system, Biomet , Download_VeroeffentlichtAm_EN PDF, 3MB, File does not meet accessibility standards