Interesting and Related LAWSUITS.

Are you or someone close to you experiencing complications due to an implant or procedure? More and more people are speaking up and the awareness is spreading about the malpractices from some of these procedures and defective mesh hernia products. It's time to do something and you or your loved one may be entitled to financial compensation. Don't delay, call today!

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August 17, 2017

Ethicon Proceed Mesh Lawsuit

On August 17, 2017, a Pennsylvania woman filed an Ethicon Proceed lawsuit in the Western District of Pennsylvania. She claims that after being implanted with the product, she suffered serious injuries.

August 22, 2017

Physiomesh Hernia Patch Lawsuit

A lawsuit has been filed by a man from Alabama who claims the Ethicon Physiomesh hernia patch caused him to develop severe complications that required another surgery after his hernia repair.

Sept. 8, 2017

Lawsuits Against Ethicon

Rheingold, Giuffra, Ruffo, & Plotkin LLP announce that they have filed a lawsuit against Ethicon, Inc., the makers of the defective Physiomesh, as well as their parent company, Johnson & Johnson. The lawsuits were filed on behalf of three patients who received Physiomesh to repair their abdominal hernias and experienced complications, such as hernia recurrences and chronic abdominal pain.

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You Or Your Loved One May Be Entitled To Financial Compensation. Don’t Delay, Call Today!
September 13, 2017

New Physiomesh Lawsuits

According to court records, new Physiomesh lawsuits were filed just last week in the U.S. District Court, Southern District of New York, on behalf of three plaintiffs who suffered hernia recurrence and other complications, allegedly due to the failure of an Ethicon device.

July 31, 2017

Arkansas Woman Suffers

An Arkansas woman filed a Physiomesh lawsuit against manufacturers Ethicon and parent company Johnson & Johnson (J&J). The plaintiff claims that after being implanted with the Ethicon Physiomesh. She seeks in excess of $75,000 in compensatory and punitive damages.

March 9, 2017

Ethicon’s Physiomesh Composite

Plaintiffs filed a Motion for Transfer for 18 lawsuits filed in nine separate courts across the country: Florida, Illinois, Georgia, Colorado, South Carolina, Kentucky, Massachusetts, Oklahoma and New Jersey.

A Class-Action Suit Over Recalled Products

Some Canadian hernia surgery patients have launched a class-action lawsuit against the maker of a now-recalled product, claiming they weren't warned of its dangers. Patients are speaking out about a surgical device called Physiomesh Flexible Composite Mesh, which was used in Canada up until last year, when it was recalled and pulled from the market over concerns about higher rates of complications. The product is made by Ethicon, a subsidiary of Johnson & Johnson. It became available on the Canadian market in September, 2010.

Ethicon sold about 330,000 Physiomesh implants worldwide. It sold about 50 percent of those products in the U.S., according to plaintiffs. Ethicon voluntarily pulled the devide from the market in May 2016 after it found higher rates of re-operation and hernia recurrence. You can read the full story here.

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