Cordis is recalling specific lots of ANGIOGUARD™ RX / XP Emboli Capture Guidewire System, Cordis has identified that there is a potential for separation of the ANGIOGUARD™ RX / XP delivery system and capture sheath. The potential impacts of separation include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke, while a replacement device is prepared. Recall start date: March 15, 2023
RecallTracker