Hernia mesh lawsuits are being filed across the country. Most of these cases involve complications from hernia surgeries, and patients have complained that the meshes caused severe pain in their abdomen area. Mesh manufactures argue there is no proof for any injury claims based on a study of adverse events reported by 1/3rd of all hospitals who use them.
Hernia Mesh Problems Cause “Horrible Pain," Lawsuits. The “hernia mesh problems years later” is a problem that has been present for a while. Hernia Mesh Problems Cause “Horrible Pain," Lawsuits.
Patients in North America continue to blame hernia mesh for unpleasant side effects, notably Ethicon’s Physiomesh and Atrium’s C-QUR products, which are both being sued for.
Last month a group of Canadians filed a complaint against Johnson & Johnson (which owns Ethicon) over debilitating health issues they say were caused by the mesh. The alleged side effects include perforations, abscesses, and Infections. Many plaintiffs say they required revision surgeries to correct these issues.
Colleen Copland, 34, alleges her mesh strained, resulting in a recurrence of her hernia. “The anguish is always there,” she tells CTV News. My insides feel like they’re about to burst… To be honest, it’s a terrible agony.”
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“You Couldn’t Even Touch Me,” says the narrator.
“You couldn’t even touch me, I’d scream, I mean genuinely cry,” Ivan Richardson said, echoing Ms. Copland’s accusations. “I went to the doctor, and they kept saying they couldn’t find anything.”
When the physicians cut him open to investigate, they discovered that the hernia mesh he’d gotten had rolled up within his body, according to Mr. Richardson.
Before Ethicon announced a global recall in May 2016, it’s believed that 30,000 Canadians had a Physiomesh implant.
“At Ethicon, our first focus is to our customers and their patients,” the company stated in a statement. “This includes the safe and effective use of our products.” Ethicon will fight any litigation that arise from the use of our hernia mesh products.”
Since 2000, Health Canada has recalled or withdrawn 12 different varieties of hernia mesh off the market.
Mesh patients in the United States have also filed lawsuits.
In the United States, hernia mesh devices have also resulted in litigation. Aside from Ethicon’s Physiomesh, Atrium’s C-QUR is facing at least 21 lawsuits from patients who claim to have suffered adverse effects as a consequence of the fish oil coating on C-QUR. The following are some of the claimed adverse effects:
- Reactions to foreign bodies
Theresa Callaway, like Ivan Richardson, claims that her mesh “rolled up” and “bunched up in layers,” causing agony, nausea, vomiting, infections, and revision procedures.
Surgical mesh has long been beset by issues like these. C.R. Bard proposed $184 million in 2011 to resolve 2,600 surgical mesh complaints brought in a multi-district action in Rhode Island (MDL).
Check out our infographic about hernia mesh.
The US Food and Drug Administration (FDA) issued a warning to Atrium in October 2012 concerning the C-QUR mesh’s risk for infections and sterility issues. The FDA announced a Class 2 device recall for the C-QUR Edge Mesh in July 2013.
James Brown filed a lawsuit against Atrium in January 2017, stating that he was implanted with the C-QUR mesh in a hernia repair procedure in 2013 but continued to have stomach discomfort. Mr. Brown claims he had revision surgery to remove the mesh in January 2016, during which physicians noticed he had a “foreign body large cell response” as well as scarring of the surrounding tissue.
The FDA announced a Class 2 device recall for the C-QUR Edge Mesh in July 2013.
Mr. Brown’s lawsuit, along with 20 others, was merged into a federal multi-district action earlier this year (MDL).
Meanwhile, the first Ethicon Physiomesh litigation in the United States is set to begin in Illinois’ Southern District in January 2018.
Complications in the mesh stifle financial forecasts.
Research and Markets noted in its five-year projection of the marketability of hernia repair devices that
Operation failure and hernia recurrence in obese and elderly patients, as well as the dangers and consequences associated with hernia repair surgery and mesh, are all limiting the worldwide market for hernia repair devices.
Tela Bio stated yesterday that it will perform a post-market clinical research of its OviTex biological mesh, which is mainly used for hernia repair and abdominal wall reconstructions, in order to discover and prevent precisely these sorts of issues.
A post-market clinical evaluation of Tela Bio’s OviTex biological mesh will be conducted.
“Surgeon feedback on OviTex performance and surgical handling has been positive so far,” said chief medical officer Dr. Maarten Persenaire in a press release. “We are excited to initiate a formal clinical data collection program that will support future efforts to refine surgical mesh design and develop new clinical protocols for hernia repair.”
Tela Bio has taken a positive step forward, although surgical mesh may need additional scientific examination and design improvement.
Contact us for a free, no-obligation legal consultation if you or a loved one had hernia repair surgery and had mesh issues.
The “is hernia mesh safe 2020” is a question that has been asked many times in the past. There have been some lawsuits regarding this topic, but there are no clear answers to whether or not hernia mesh is safe.
Frequently Asked Questions
Can hernia mesh cause problems years later?
A: There are a lot of things that can cause problems years later. It is best to consult with your doctor if you are unsure about what is causing the pain, especially because hernia mesh surgery often involves multiple procedures.
What are symptoms of hernia mesh problems?
A: A hernia mesh is a synthetic piece of fabric that goes around and supports the area where your bodys internal organs normally reside. Depending on which type you have, it can sometimes cause pain, swelling or bleeding in one or both sides of your abdomen.
What causes hernia mesh failure?
A: There are a number of possible causes for hernia mesh failure which includes but is not limited to, trauma from surgery or childbirth, infection and inflammation.
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