Consult an Essure Lawyer if You Were Injured by This Dangerous Device Bayer’s permanent birth control device, Essure, has officially been removed from the market. The company announced in July that it planned to discontinue sales at the end of 2018 due to declining profits. However, many consumers have argued that the device was not safe to begin with. While
Why You Need a Defective Medical Device Lawyer When Facing the Horrifying Truths of the Big Medical Industry A shocking Netflix Original documentary, The Bleeding Edge, exposes the dark underbelly of the $400 billion medical device industry in America. The large industry is responsible for many defective medical devices including hernia mesh, hip implants, and IVC filters, all of
You had your hernia repaired with hernia mesh, but you just don’t seem to be doing any better. Maybe you even feel worse. Also known as physiomesh, hernia mesh isn’t always well tolerated by the body. Your body may reject it or the mesh may actually fail. Both rejection and failure of the mesh can be a medical emergency. Why
Hernia mesh lawsuits filed against Atrium, manufacturer of C-Qur mesh, continue. Recently, one plaintiff alleged that he suffered more than an injury from the mesh. James Brown, who was a recipient of C-Qur mesh to correct an umbilical hernia, also alleged that the materials used to manufacture it are biologically incompatible with human tissue. What Is C-Qur Mesh Made From?
Women who undergo a hysterectomy or fibroid removal in which a power morcellator is used run the risk of spreading undiagnosed cancer throughout the rest of their body. How did this happen? Why did the FDA approve power morcellators and what did they do after learning about the cancer risks to women? Power Morcellators Approved Without Testing Power morcellators for