Physiomesh Hernia Repair Patches Are The Subject Of Growing Litigation

Hernia repair surgery is very common in the US, with the US Food and Drug Administration (FDA) reported that more than one million such procedures take place nationwide each year. For many patients, this course of treatment involves the use of surgical mesh as a means of facilitating the healing that takes place.

There are concerns about the safety Physiomesh Ethicon hernia repair product, which has been available in the US market since 2010. Plaintiffs around the country have started filing a case through Ethicon hernia mesh lawsuits or physiomesh injury lawyers to secure compensation for the damages and the serious side effects they consider are directly caused by the patch Physiomesh.

Key Facts Regarding Physiomesh Hernia Repair Products

As defined by the FDA, surgical mesh, involving those utilized in hernia repair methods, designed to offer additional support for network regions that have been damaged or weakened.

Physiomesh patch composed of fibers made from flexible woven plastic to create a mesh that aims to prevent internal adhesions that while surgical repair itself given time to take root and become permanent.

Although it has been suggested that the use of these types of products mesh has a strong track record for improving surgical outcomes, an increasing number of patients have stepped forward stating that the product Physiomesh, in particular, has the potential to cause serious damage.

Whereas the scope of eventual hernia mesh litigation remnants to be seen, the lawyer continues to review potential cases to determine how best to proceed on behalf of patients who suffer from what could be a life-changing side effect.