BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Lactosorb Trauma Plate, Biomet

Product group Non-active implants
Reference 01336/08

Lactosorb Trauma Plate: The company Biomet has informed about a recall of several lots of these products. The action was initiated because of a complaint, which identified that the item may not have been sealed properly (outer package). The sterile barrier may be compromised.

Recall for Lactosorb Trauma Plate, Biomet , Download_VeroeffentlichtAm_EN PDF, 100KB, File does not meet accessibility standards