BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lots recall of 200 mm EverFlexTM, ev3 Incorporated

Product group Non-active implants - special implants
Reference 05639/13

The manufacturer ev3 Incorporated recalls certain lots of the 200 mm EverFlexTM self-expanding peripheral stent with EntrustTM Delivery System because of reported deployment issues.

Lots recall of 200 mm EverFlexTM, ev3 Incorporated , Download_VeroeffentlichtAm_EN PDF, 143KB, File does not meet accessibility standards