According to an online news report published on medicaldevice-network.com, the U.S. Food and Drug Administration has announced a Class I recall of Zimmer's ROSA One 3.1 Brain Application.  The recall affected around 120 devices sold in the United States.  Zimmer initiated the recall of the platform, indicating software problems.  A … [Read more...] about Zimmer ROSA One 3.1 Brain Application Recalled