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Canadians Join Hernia Mesh Class Action Lawsuit

justice scales & gavel in front of Canadian flag

As Americans continue to file hernia mesh lawsuits, Canadians began their hernia mesh class action claiming they weren’t warned of the implant’s risks.

The device at the center of the claims is Ethicon’s Physiomesh Hernia Mesh which Health Canada recalled in 2016. The Canadian agency’s action came after it learned that recurrence and reoperation rates with the device were higher than those of other meshes.

After the recall, Canadians who received Physiomesh suffered severe pain and had to undergo additional surgeries to repair hernias that reoccurred.

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Canadian lawyer Jill McCartney is representing plaintiffs in the class action. She told CTV News that plaintiffs had their hernias “come back with greater severity.”

“It is our understanding that there are more people out there, and there’s probably more people that are experiencing these kinds of side effects,” McCartney said.

Hernia mesh recipients wonder how the product was approved for use in the first place.

“I think there should be more testing on these products and not so quick to get them onto the market if they’re not ready,” Colleen Copland, one of the plaintiffs awaiting a second hernia surgery, told CTV News.

Ethicon said it would defend against the lawsuits. The company voluntarily pulled Physiomesh from the U.S. market in May 2016 but called it a withdrawal and not a recall.

Hernia Mesh Brands in U.S. Lawsuits

Americans who received Physiomesh are also facing the same complications, including severe pain, abbesses, infections and organ perforation. Ethicon faces growing litigation from Physiomesh in the U.S.

In addition to Physiomesh, other brands are also the subject of lawsuits in state and federal courts. Manufacturers include Ethicon, C.R. Bard, Atrium and others.

About two dozen lawsuits are pending in the newly created Atrium C-QUR hernia mesh multidistrict litigation (MDL) in New Hampshire before Judge Landya B. McCafferty. McCafferty recently appointed plaintiff’s attorney D. Todd Matthews to lead the MDL. Matthews is a part of a five-member Plaintiff’s Executive Committee.

“The injuries these plaintiffs have suffered are horrific. I certainly plan to honor the court and the victims of this product by working hard and doing everything in my power to see that justice prevails,” Matthews said in a statement.

According to Atrium’s marketing, the fish oil coating on C-QUR mesh is supposed to prevent it from adhering to the bowel. But, plaintiffs in the MDL allege Atrium’s mesh sticks to the bowel and other organs causing ulcers, infections, bowel obstructions and other complications.

Hernia Mesh Maker Paid Millions in Settlements and Verdicts

C.R. Bard was one of the first companies to recall its hernia mesh implant — the Kugel Composix Hernia Patch. Following the recall, the company faced thousands of lawsuits. In the second bellwether trial, the jury found Kugel Patch was defective and awarded $1.5 million to the plaintiff Christopher Thorpe in 2010.

The following year, the company settled more than 2,600 lawsuits for $184 million.

While Ethicon has not discussed settlement for any of its U.S. Physiomesh cases, one of the first Physiomesh lawsuits filed by Matthew Huff heads to trial in January 2018.

Michelle Llamas, Senior Content Writer
Written By Michelle Llamas Senior Writer

Michelle Llamas has been writing articles and producing podcasts about drugs, medical devices and the FDA for nearly a decade. She focuses on various medical conditions, health policy, COVID-19, LGBTQ health, mental health and women’s health issues. Michelle collaborates with experts, including board-certified doctors, patients and advocates, to provide trusted health information to the public. Some of her qualifications include:

  • Member of American Medical Writers Association (AMWA) and former Engage Committee and Membership Committee member
  • Centers for Disease Control and Prevention (CDC) Health Literacy certificates
  • Original works published or cited in The Lancet, British Journal of Clinical Pharmacology and the Journal for Palliative Medicine

2 Cited Research Articles writers follow rigorous sourcing guidelines and cite only trustworthy sources of information, including peer-reviewed journals, court records, academic organizations, highly regarded nonprofit organizations, government reports and interviews with qualified experts. Review our editorial policy to learn more about our process for producing accurate, current and balanced content.

  1. Coorsh, K. (2017, March 28). Canadian patients join class-action over recalled hernia mesh. Retrieved from
  2. Edwardsville Intelligencer. (2017, March 10). D. Todd Mathews named to lead Atrium C-Qur Hernia Mesh Litigation. [Press Release]. Retrieved from
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