Some who were promised a solution in Johnson & Johnson’s Ethicon Physiomesh Flexible Composite hernia mesh instead found themselves facing potential infections, hernia recurrence, and additional surgeries. Ethicon Hernia Mesh first entered the market in April 2010 for hernia repair procedures, but it did so without FDA review or clinical trials to evaluate its safety. If you or a loved one has suffered complications, a Charlottesville Ethicon hernia mesh failure lawyer can review your case and help you understand your legal options.
Contact our experienced medical malpractice attorneys today.
Ethicon Physiomesh is a coated hernia mesh with a thick protective layer on both sides. The coating is designed to prevent the bowel from direct exposure to polypropylene, a material that adheres to human tissue. If polypropylene attaches to the bowel, it can cause severe internal injuries.
However, when the coating completely covers the polypropylene, the mesh does not properly incorporate into the abdominal wall. As a result, the Physiomesh can float or migrate within the abdominal cavity, leading to dangerous complications.
Patients implanted with Ethicon Hernia Mesh have reported serious health issues, including:
Pain
Swelling
Adhesions
Obstructions
Mesh migration
Bacterial infections
Hernia recurrence
Additional surgeries to treat recurrence
In 2016, Johnson & Johnson voluntarily recalled the Ethicon Physiomesh from the global market. This decision followed two independent analyses that found recurrence and reoperation rates for patients with Physiomesh were significantly higher than average.
If you or your loved one suffered complications after hernia repair with Ethicon Physiomesh, legal options may be available. A Charlottesville Ethicon Hernia Mesh Failure Lawyer at MichieHamlett can investigate your case, consult with medical experts, and guide you through the claims process. Our team is committed to pursuing accountability and helping you seek the compensation you deserve. Contact us today for a free consultation.