Although plaintiffs predict that a growing number of Atrium ProLoop and Prolite lawsuits are likely to be filed, the JPML determined that with only 11 cases currently pending formal centralization is not justified
Plaintiffs have asked the panel to consolidate the hernia mesh lawsuits in a central California federal court for pretrial proceedings.
Although similar allegations of problems with Atrium ProLoop and ProLite mesh have been presented in lawsuits filed in federal courts, manufacturer maintains formal coordination is not necessary
The lawsuits claim polypropylene is an inappropriate substance to use for Atrium ProLite and ProLoop hernia mesh implants, which can result in severe, permanent injuries.
Plaintiff claimed mesh was not sterile, causing infections and other adverse health effects after hernia repair
