Have you suffered from hernia mesh complications? If so, you may be eligible to receive monetary damages. Hernia mesh devices have been associated with design defects that could lead to revision surgeries and other life-threatening injuries. Serious health consequences include severe abdominal pain, infection, bowel obstruction, adhesions/perforation of tissue and/or migration of the hernia mesh implant. Product failure can also lead to a hernia recurrence. Financial compensation may be available. Settlements could be on the horizon soon, but time is limited. Contact us today for a free case review.
To qualify, one must have received a hernia mesh implant from 2011 to the present, have undergone a revision surgery (or surgeries) and/or have one that is presently scheduled. Specifically, we are looking for individuals affected by the following hernia mesh products: Bard, Proceed, Prolene Hernia Systems, Covidien/ Medtronic/Tyco, Prolite, Proloop, C-Qur, Alloderm, Xenmatrix, or Ultrapro. Since most people don’t know which one they had, we’ll gladly obtain the medical records.
Here is more info about the lawsuit: A 2016 study of those who’d had hernia mesh surgery found that roughly 1 in 3 participants required an additional procedure(s) to correct issues that arose in the first five years. Common complications include severe pain and damage to the bowels, intestines, and abdomen. Sadly, the manufacturers knew about the severe impact that their product may cause. In order to protect their “bottom line,” however, they failed to warn consumers about the dangers in order to avoid issuing product recalls.
Don’t suffer in silence! Let us seek justice for your medical bills, loss of a loved one, income, pain and suffering and/or emotional distress.
We are here to help!
