For Second Time This Month, Medtronic Announces Class I FDA Recall Related To HeartWare System Component
Baxter Volara Recall Classified; BD Faces Bone Needle Recall
Medtronic, Baxter and BD are all facing recalls, with Medtronic finding yet another issue with HeartWare HVAD systems. Separately, the FDA put a Baxter respiratory device recall into Class I, and BD announced a recall on intraosseous devices.
