Penumbra Jet 7 Xtra Flex Catheter Recall
The Food and Drug Administration (FDA) announced today that Penumbra has recalled all units of the Penumbra Reperfusion Catheter with Xtra Flex Technology (Jet 7 Xtra Flex) due to increased risk of serious injury and death while removing blood clots in stroke patients. Free Consultation The Penumbra Jet 7 catheter recall comes after the FDA received over 200…