Federal medical device law bars claims against
The U.S. District Court for the Central District of California, in two Aug. 27 opinions, threw out 16 suits by the women who say they were harmed when their implants ruptured or leaked silicone.
The Food and Drug Administration granted premarket approval to Mentor in 2006, subject to certain conditions including a requirement that it conduct safety studies on the implants.
Federal law generally blocks suits involving ...
Learn more about Bloomberg Law or Log In to keep reading:
See Breaking News in Context
Bloomberg Law provides trusted coverage of current events enhanced with legal analysis.
Already a subscriber?
Log in to keep reading or access research tools and resources.