BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Voluntary Recall of Anaconda™-ONE-LOK Bifurcate Body and Anaconda™ Bifurcate Body, VASCUTEK Ltd.

Product group Non-active implants - special implants
Reference 06372/13

VASCUTEK Ltd. recalls all lots of Anaconda™-ONE-LOK Bifurcate Body and Anaconda™ Bifurcate Body from the market. The recall addresses potential patient risks associated with the wire fracturing and the possibility of conversion to open repair.

Voluntary Recall of Anaconda™-ONE-LOK Bifurcate Body and Anaconda™ Bifurcate Body, VASCUTEK Ltd. , Download_VeroeffentlichtAm_EN PDF, 2MB, File does not meet accessibility standards