BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall for the Optipac Refobacin Revision 40, BIOMET

Product group Non-active implants - materials for implants
Reference 02071/13

Optipac Refobacin Revision 40: The company BIOMET has informed about a lot recall of this bone cement. The action was initiated because of a labelling error of devices (a mistaken name, reference- / lot-no. and expiry date).

Lot Recall for the Optipac Refobacin Revision 40, BIOMET , Download_VeroeffentlichtAm_EN PDF, 187KB, File does not meet accessibility standards