Recall of Impact attachment ND270Rfor pre-assembled Plasmacup® delta, Aesculap AG
2009.09.01
Product group Medical instruments for use in humans
Reference 03091/09
Aesculap AG recalls the Impact attachment for pre-assembled Plasmacup® delta, because of the possibility of loosening of the green ball head during the implantation process.The device is marketed in Germany, not in any other country within the EEA, also not in Switzerland. Advisory Notice is only available in German language.