Guidant voluntarily recalls Multi-Link Vision stent
This article was originally published in Clinica
Executive Summary
Guidant has voluntarily recalled its Multi-Link Vision coronary stent system shortly after a limited market introduction in Europe and Australia. The recall follows reports that some stents have become dislodged from the delivery system; the cause of this is to be investigated. The company said that patients who have already received the device are not affected by the recall.