Ethicon Hernia Mesh Lawsuits
Medical Device Lawyers Serving All of the U.S.
Anyone can develop a hernia. They’re caused by weakened muscles and increased pressure on the stomach or intestines. For some people, surgery can help relieve the pain caused by hernias. During a hernia operation, doctors often use synthetic mesh to reinforce the weakened area.
One type of hernia mesh, the Ethicon Physiomesh Flexible Composite, has been recalled for causing infections and surgeries.
Our hernia mesh lawyers are now accepting cases involving injuries from this implant. Call (800) 794-0444 today - you pay no fee unless we win your case, so the best time to call is now.
Patient Injuries and Global Recall
Information from two large hernia registries showed that patients implanted with Ethicon’s Physiomesh had higher than normal rates of hernia recurrence and reoperations. In other words, the Ethicon mesh failed more often than other hernia mesh products. As a result, in May 2016, Ethicon recalled the Physiomesh Flexible Composite Mesh from global markets.
Complaints of serious injuries have mounted since this mesh was put on market in 2010. Physiomesh was approved under a special clearance, so it didn’t go through any testing before being used in patients.
Among the injuries caused by the Ethicon Physiomesh include:
- Additional surgeries
- Bowel perforation
- Device failure
- Device migration
Our Experienced Mesh Attorneys are Here to Help
Pintas & Mullins Law Firm has fought for patients harmed by medical devices for 30 years, winning millions for our clients and their families. We’ve been working on other defective mesh product cases for many years, including transvaginal mesh, pelvic mesh, and hernia patch lawsuits.
Our Chicago medical device lawyers continue to represent clients in transvaginal, pelvic, and hernia mesh lawsuits nationwide. We do not charge anything unless we win you a settlement or verdict, and our reviews are always free.