www.fdanews.com/articles/161996-jjs-codman-neuro-recall-upgraded-to-high-risk-class-i
J&J’s Codman Neuro Recall Upgraded to High Risk Class I
January 24, 2014
Codman Neuro, a division of Johnson & Johnson 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.
MassDevice
MassDevice