A lawsuit has been filed that alleges that Physiomesh is defective and that Johnson & Johnson and its Ethicon associate are therefore legally responsible for harm caused by its manufacture, marketing, and sale.

Physiomesh, a flexible composite mesh produced by Ethicon, Inc., is used to repair hernias in both the stomach and groin areas.  Such hernias occur when a small portion of the intestine bulges through an opening in the muscles of the abdominal wall, and are typically caused by heavy exertion, age, or genetic factors. Fixing a hernia generally requires a minimally invasive surgery to repair the broken abdominal wall; mesh products like Physiomesh are placed beneath the abdominal wall in order to prevent a hernia from recurring after the surgery is completed.

In May 2016, Ethicon started a voluntary recall of the mesh after reviewing information received from two independent hernia registries. Within those registries, the number of hernias requiring additional surgeries was higher among patients who received Physiomesh than those that did not. Ethicon believes that the higher rate is a result of a number of different factors, of which many are beyond their control. However, Ethicon has not been able to specifically identify those factors. As a result, Ethicon recalled Physiomesh from the global market. (Ethicon “Urgent: Field Safety Notice” May 25, 2016).

At McDivitt Law Firm, we believe that everyone is entitled to information that may be relevant to their rights as a consumer. If you or someone you know has received Physiomesh after a hernia, please contact us for a free and confidential case evaluation.