About Jet7

After more than 200 reports of serious injury and death associated with a JET 7 Xtra Flex catheter defect, Penumbra has issued a voluntary recall of their product.

According to the U.S. Food and Drug Administration, the hundreds of reports filed with the FDA’s Manufacturer and User Facility Device Experience (MAUDE) Database included instances of serious injuries and even 14 patient deaths associated with the Penumbra catheter.