"Tip separation" leads Endologix to recall Powerlink delivery catheters
This article was originally published in Clinica
Executive Summary
Irvine, California-based Endologix has issued a voluntary recall in the US involving around 35 catheters that are used to deliver its Powerlink stent graft in patients suffering from abdominal aortic aneurysms (AAA). As the recall concerns only the delivery system, patients that have already been implanted with the stent graft will not be affected.