Johnson and Johnson Hernia Mesh Harming Women

Another Johnson and Johnson product is receiving adverse reports for complications and mesh failure. This product is the Johnson and Johnson Ethicon hernia mesh. In our continuing attempt to help women injured by dangerous drugs, devices and consumer products, we have lawyers filing hernia mesh lawsuits for victims.

Physiomesh Causing Complications

 

The Physiomesh is a flexible composite mesh that is used in hernia repair.  It is made from  polypropylene, the same  mesh is also used to reinforce the vaginal wall in transvaginal mesh surgery.  This the same vaginal mesh that has been falling apart in women.

Johnson and Johnson Withdraws Physiomesh

In May of 2016, Ethicon  issued a worldwide recall of Physiomesh. The recall was based on the fact that the medical product was associated with a higher risk of  complications, including the need for additional surgeries. Many women who underwent hernia repair surgeries that used Physiomesh experienced mesh failure  events.

What Are The Dangers of Physiomesh?

Abdominal pain;
Necessary revision surgery to remove Physiomesh;
Recurrence of hernia;
Infection;
Erosion;
Perforations;
Device failure;
Bowel obstruction;
Fever;
Constipation;
Mesh migration;
Mesh contraction;
Intestinal fistulae;
Sepsis;
Diarrhea; and
death.

FDA On Physiomesh

A November 2010 report notes  “tears, rips, holes in device” are reported, leading to “minimal adhesion” and removal of the mesh. A February 2012 report in which a patient, who underwent hernia repair surgery that used Physiomesh, returned one week  after surgery with complaints of vomiting, constipation, and abdominal pain and distention. The  symptoms were a result of the Physiomesh. Ethicon did issue a voluntary recall  and was not mandated by the FDA to do so.

Physiomesh Lawyers Filing Physiomesh Lawsuits

Have you had  hernia repair surgery and have experienced any symptoms of mesh failure?  Contact us for a physiomesh lawyer.

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