1. FDA Recall: J&J MedTech/CERENOVUS CEREPAK Detachable Coil System Removed Due to High Failure-to-Detach Rate
Johnson & Johnson's MedTech division, operating through its CERENOVUS Inc. subsidiary, has initiated a removal of its CEREPAK Detachable Coil System from the market. The action is being taken in response to a higher-than-expected rate of device failure, specifically a failure of the coil to detach from its delivery sys...