Injuries Linked to the Penumbra JET 7 Xtra Flex Catheter Recall
Injuries Related to the Penumbra JET 7 Xtra Flex Catheter On December 15, 2020, the U.S. Food and Drug Administration (FDA) notified the public that Penumbra, Inc. had issued a voluntary recall of their Penumbra JET 7 Xtra Flex catheter due to reports of the product causing serious injuries and even death. The notice warned that…