Recall for Visi-Pro Balloon Expandable Stent System, ev3 Inc.
2008.07.25
Product group Non-active implants
Reference 02656/08
Voluntary recall of specific lots of the Visi-Pro balloon expandable stent system of the US manufacturer ev3 Inc. This recall is being conducted because the stent system may not have adequate securement to the delivery system and may have a larger diameter/profile than intended. This potential issue is manifest only during the procedure, this measure does not affect patients who have already received treatment.
Recall for Visi-Pro Balloon Expandable Stent System, ev3 Inc. , Download_VeroeffentlichtAm_EN