BfArM - Federal Institute for Drugs and Medical Devices

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Product group Non-active implants
Reference 01950/08

Recall of a specific lot of the self-expanding peripheral stent Protégé EverFlex of the US manufacturer ev3 Inc. due to mislabelling. The use of this mislabelled stent could result in a delay of the procedure.

Recall Protégé EverFlex, ev3 , Download_VeroeffentlichtAm_EN PDF, 74KB, File does not meet accessibility standards