Richards v. Legacy Health, et al.

Summary

In this pelvic mesh trial, plaintiff Tamarie Richards relied upon Boston Scientific’s transvaginal mesh to treat her pelvic organ prolapse. This mesh was installed on the same day the FDA issued a relevant manufacturer’s notice, and caused numerous lasting issues for Richards after installation. Richards dealt with pudendal neuralgia in the aftermath of this procedure and was forced to undergo additional surgery to remove parts of the mesh. Richards claims that Dr. Michael Lemmers and Legacy Health did not fully discuss the FDA’s updated device risks with her.

Dr. Lemmers and Legacy Health claim they fully covered alternative treatment methods, even presenting the updated FDA guidelines to Richards the morning of surgery. Additionally, they emphasize Dr. Lemmers’ history of successful mesh installation, which he had used for decades with no problems arising.

Outcome

Verdict For Defense.