Johnson & Johnson's Codman Neuro Recall Elevated To High Risk Class I

Johnson & Johnson subsidiary Codman Neuro's recall of its Trufill n-BCA liquid embolic system gets labeled as a Class I measure by the FDA. Codman Neuro, a division of Johnson & Johnson (NYSE:JNJ) subsidiary DePuy Synthes, said the FDA labeled its Trufill n-BCA liquid embolic system recall as Class I, the federal watchdog agency's highest-risk classification. The Raynham, Mass.-based company develops devices for neurosurgery, neurovascular repair and neuromodulation.

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