BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of all Vega Tibia Extension stems, Aesculap

Product group Non-active implants
Reference 02033/11

Aesculap informs about a recall of all Vega Tibia Extension stems as during implantation stem breakage can occur in the hexagon connection to the torque wrench.

Recall of all Vega Tibia Extension stems, Aesculap , Download_VeroeffentlichtAm_EN PDF, 42KB, File does not meet accessibility standards