FDA Sends Warning Letter Regarding Zimmer Trilogy Hip System
In September 2012, the FDA sent a warning letter to Zimmer Holdings regarding its manufacturing facility in Ponce, Puerto Rico. The company indicated in a report to the SEC that the FDA had warning them of certain problems with product testing. Zimmer indicated that it has already corrected some of the issues and was working on the FDA's remaining concerns. It is likely that these issues will be cited in pending Zimmer hip replacement lawsuit complaints. Anyone who has been injured from an affected product should contact a Zimmer hip lawyer to discuss the requirements of a Zimmer hip lawsuit.