Preview Newsletter

Ethicon Media Monitoring 1/19/2018

    Client Attorney Privileged/Attorney Work Product/At Request of Counsel

    Online Sources

  1. Surgical mesh campaigner calls for Welsh Government ban on use

    Jan 18, 2018 | Barry And District News

    A GRANDMOTHER has joined the ranks of campaigners calling on the Welsh Government to take action on the use of polypropene mesh saying it has it left her with a “lifetime of pain”.
  2. Ethicon Physiomesh Plaintiff Starts New Year with Hernia Mesh Lawsuit

    Jan 18, 2018 | Lwyers and Settlement

    By Gordon Gibb

    Gerald Payne tried to soldier on in spite of the pain. After seven years, he finally underwent surgery to remove the Ethicon Physiomesh that was the cause of all his problems.

    Client Attorney Privileged/Attorney Work Product/At Request of Counsel

    Online Sources

  1. Surgical mesh campaigner calls for Welsh Government ban on use

    Jan 18, 2018 | Barry And District News

    A GRANDMOTHER has joined the ranks of campaigners calling on the Welsh Government to take action on the use of polypropene mesh saying it has it left her with a “lifetime of pain”.

    Barry resident Pauline Inch has described how keyhole surgery to remove her gall bladder went wrong and the surgical mesh was implanted to solve problems which arose subsequently.

    The former civil servant, 61, of Newlands Road, has been in contact with Vale AM Jane Hutt and says she wants ministers to ban the material’s use to prevent other patients undergoing a similar ordeal.

    Surgeons use surgical mesh as a medical tool to support organs within the body.

    It has a variety of functions, but is commonly used to rectify bowel and bladder problems.

    A campaign calling for the ban of the medical device has gained traction in recent years with recipients reporting experiencing severe, chronic pain following surgery, immediately after or years later.

    Some women have been left in agony, unable to walk, work, or have sex when the mesh erodes and slices into organs.

    Mrs Inch said: “In 2000 I had keyhole surgery to remove my gall bladder. I was told it would be straightforward.

    “Within hours I was having life-saving surgery.”

    Subsequently mesh was implanted in 2004 to remedy a hernia and in 2013 it was found that the mesh had wrapped around her organs and her body was rejecting the mesh.

    Mrs Inch is now in constant pain and virtually housebound having lost her formerly active life.

    The mesh can never be removed.

    She said: “It’s like a Chinese burn inside and there’s also a feeling like a barbed wire pain. I cannot sleep through the pain. I have polypropene mesh inside me which is poisoning me.”

    A Welsh Government spokeswoman said the working group on vaginal mesh was expected to complete its research at the end of January and would report after that.

    Vale AM Jane Hutt said: “I have been supporting patients suffering from adverse effects of polypropylene mesh and tape since 2012, and will be attending a meeting with the health secretary about the issues next week.

    “I welcome the formation of the Welsh Mesh Working Group by the cabinet secretary for health.”

    http://www.barryanddistrictnews.co.uk/news/15865335.Surgical_mesh_campaigner_calls_for_government_ban_on_use/

    Return to headline | Return to top

  2. Ethicon Physiomesh Plaintiff Starts New Year with Hernia Mesh Lawsuit

    Jan 18, 2018 | Lwyers and Settlement

    By Gordon Gibb

    Gerald Payne tried to soldier on in spite of the pain. After seven years, he finally underwent surgery to remove the Ethicon Physiomesh that was the cause of all his problems. 

    Atlanta, GA It’s one thing for a medical device to result in unwanted side effects and adverse events. However, that frustration is further exacerbated when the medical device thought to be at the root of newfound pain and suffering, has failed to do its intended job in the first place. Thus, the original implantation was all for naught. That’s the claim made by a recent surgical mesh lawsuit involving the now-recalled Ethicon Physiomesh filed last week in Idaho.

    The hernia patch lawsuit was filed by plaintiff Gerald Payne. According to Court documents, Payne underwent a laparoscopic ventral incisional hernia repair in August 2010 with the Ethicon Physiomesh. However, rather than the relief he expected, Court records suggest that Payne almost immediately began experiencing what turned out to be chronic pain from the area into which the hernia mesh had been implanted. A noticeable bulge had developed in the location where the mesh had gone in.

    Plaintiff suffered for seven years

    Payne’s surgical mesh side effects lawsuit further asserts that Payne suffered weakness, loss of core strength, nausea, and was reduced to wearing a binder across his abdomen. The plaintiff asserts to have soldiered on in the midst of much pain and discomfort until August of last year – seven years after the surgery – when we finally went to the emergency room for tests that determined the problematic mesh was causing an intestinal blockage – specifically a hernia mesh bowel obstruction.

    This required a subsequent procedure to have the Ethicon Physiomesh removed by way of revision surgery. The surgeon tasked with removing the Ethicon product noted the mesh had failed to adhere to the plaintiff’s muscle, as the mesh was originally designed to do.

    After a number of years on the market, Ethicon Physiomesh was pulled from circulation by the subsidiary of Johnson & Johnson (J&J) in 2016. Ethicon issued a recall and removed all remaining specimens of mesh from the market – but not before countless patients had been implanted with the now-recalled device. Hernias are a common ailment affecting a large cross-section of the aging Baby-Boomer demographic, with treatment options in recent years favoring less-invasive, laparoscopic surgery.

    Ethicon pulled the plug on its Physiomesh due to an increasing number of reports of failures. However, plaintiffs behind many a surgical mesh complications lawsuit assert that Ethicon was well aware of problems with its product long before the recall – and even before the mesh was employed in Payne’s own hernia repair in 2010.

    Lawsuit asserts Ethicon knew about problems before the 2010 surgery

    “Prior to the time that the Product was implanted in Plaintiff, Defendant was aware of numerous defects in the Product,” the lawsuit states. “Despite being aware of the numerous defects and unreasonable risks in the Product, Defendant manufactured, marketed, and distributed the Product with the intent they would be implanted in patients. Defendant was aware that implanting the Product in patients was likely to cause injury and harm to the patients into whom the Product was implanted.”

    Payne’s surgical mesh complications lawsuit further alleges the plaintiff has been unable to work since the revision surgery, which occurred in November of last year.

    The surgical mesh side effects lawsuit will join others consolidated for pre-trial motions and discovery in multi-district litigation housed before US District Court Judge Richard Story in the US District Court, Northern District of Georgia (IN RE: Ethicon Physiomesh Flexible Composite Hernia Mesh Products Liability Litigation, Case No. 1:17-md-02782).

    The individual hernia mesh lawsuit is Gerald Payne v. Ethicon, Inc., Case No. 1:18-cv-00016-DCN, filed January 10, 2018 in the US District Court for the District of Idaho.

    https://www.lawyersandsettlements.com/articles/mesh-complications/surgical-mesh-lawsuit-hernia-10-22813.html

    Return to headline | Return to top

Add recipients

Suggested