Hernia mesh devices linked to revision surgeries and life-threatening complications. Did you undergo revision surgery after receiving a hernia mesh implant? You may be entitled to compensation.
Many hernia mesh products were rushed to the market using an FDA clearance process. this process allowed them to be manufactured and marketed with little to no studies about the safety of the devices.
Hernia mesh devices found to be associated with design defects that could lead to revision surgeries and life-threatening complications.
Due to the rushed FDA clearance and the lack of research done on the devices prior to release, many hernia mesh devices were silently withdrawn or recalled from the market.
Hernia mesh devices contain design defects and undisclosed or under-disclosed risks such as: excessive mesh and tissue contraction; tendency of the mesh to migrate, shrink, or turn into a hardened ball or mass; excess foreign body reaction and rejection of the mesh in the body.
Hernia mesh implants were linked to excessive mesh and tissue contractions.
Tendencies of the mesh to migrate or shrink which led to rejection of the mesh in the body.
Many patients had to undergo revision or removal surgeries.
C.R. Bard® Paid $184 Million To Settle Roughly 3,000 Lawsuits
CR Bard® agreed to pay $184 million to settle most of the lawsuits against its hernia repair products. Through 2011, thousands of plaintiffs had filed lawsuits for personal injuries, with most of those cases since transferred to the U.S. District Court for Rhode Island. Hernia mesh settlements were divided into different tiers based mainly on how severe the injuries were and how strong their case was.
Read this article for more information on the hernia mesh lawsuit.
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