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Atrium C-Qur Mesh Lawsuit Filed in New Hampshire

A New Hampshire man has filed a lawsuit against the manufacturer of a hernia patch that has been linked to reports of internal injuries, infection and mesh failure.

A New Hampshire man has filed a products liability lawsuit against Atrium Medical Corp., the manufacturer of a hernia patch that has been linked to reports of internal injuries, infection and mesh failure.

Free Confidential Lawsuit Evaluation: If you had an infection, gastric ulcer or other hernia mesh complications, you should contact our law firm immediately. You may be entitled to compensation by filing a suit and our lawyers can help.

What’s the Problem?

February 27, 2017 – According to the lawsuit, Plaintiff underwent hernia repair with an Atrium C-Qur patch in December 2013 after being diagnosed with an umbilical hernia. A few months after the surgery, he began suffering extreme abdominal pain.

In 2015, Plaintiff learned that the surgical mesh may be the cause of his problems, and in January 2016 had surgery to remove the hernia patch. However, he still has severe abdominal pain in the same area, according to the lawsuit.

A subsequent investigation revealed that Plaintiff had a severe allergic reaction to the mesh, which resulted in scar tissue forming around the patch. Plaintiff alleges that not only was Atrium Medical aware of the potential for this type of hernia patch reaction, but also that the manufacturer lied to the FDA about changes it made to the design of the mesh.

Furthermore, Plaintiff claims that Atrium downplayed the possibility that C-Qur could cause severe health complications in patients with fish allergies (the hernia patch is coated in fish oil). He says the company failed to notify the agency about changes it made in coating the device with this substance.

Plaintiff alleges that Atrium Medical was negligent in designing its C-Qur mesh, and schemed to convince physicians it was safe even though the company had evidence to the contrary.

Finally, plaintiff claims that Atrium failed to either investigate or fully disclose adverse event reports to the FDA, in addition to recalling several models of the C-Qur mesh without notifying the agency, patients or the healthcare community.

Do I Have an Atrium C-Qur Mesh Lawsuit?

The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Atrium C-Qur Hernia Mesh Lawsuits. We are handling individual litigation nationwide and currently accepting new injury cases in all 50 states.

Free Case Evaluation: Again, if you suffered from hernia mesh complications, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.

Free Confidential Case Evaluation

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