This website provides the details of the hernia mesh lawsuits, settlements and recalls. The kugel mesh patch was first recalled in 2005, after the fda received reports that the composix kugel mesh patch had caused many severe injuries. Composix kugel mesh patches lawsuit individual claims. As a result of some of the complications arising from these surgical meshes, the fda has recalled a variety of hernia mesh implants over the years. Certain types of hernia mesh are associated with several adverse health issues. Ventralex hernia patch medium circle with strap diameter 6. Barddavol composix, and other hernia plugs linked to safety risks. Biological hernia mesh is derived from animal tissue usually cow or pig skin or intestine that is disinfected before it is implanted. Why physiomesh is off the market agconexus 20170912t16. It has a specially designed memory coil ring that opens the patch after it is placed behind the area of the hernia.
Thousands of people have been injured by recalled hernia mesh patches. Hernia mesh lawsuit settlement amounts april 2020 update. Bard hernia mesh lawsuit dangerous side effects reported. This patch however was recalled by bard as a result of reports of various complications arising from its use. Bard, were granted regulatory clearance under the u. The patch is used to laparoscopically repair hernias in multiple locations in the body. Recall or not, if your hernia mesh is causing you pain and complications, please speak to a mesh attorney. Since the first hernia mesh recalls, there have been thousands of lawsuits against the manufacturers of these patches. The implant was made of polypropylene and contained a ring around the mesh. However, gore hernia mesh has been known to malfunction for a variety of reasons and cause even more suffering to the patient. Under this designation, the company whose product is recalled must notify customers and advise them to notify intended recipients of the recall. The device classification name is mesh, surgical, polymeric. The ventrio st patch is an ovalshaped patch made from polypropylene mesh with woven monofilament fibers. If you or somebody you know was injured by a recalled hernia patch, you should contact our lawyers immediately for a free case consultation.
Ventralex hernia mesh lawsuit ventralex hernia patch. There are already thousands of hernia mesh lawsuits filed against the manufacturers of various hernia mesh products for the injuries they have allegedly caused. The ventrio st is one of several mesh products davol produces uses its sepra technology, a hydrogel barrier on one side of the mesh that is designed to. Bard davol recalled its kugel patch hernia mesh in 2005. Additionally, ethicon, the maker of physiomesh voluntarily pulled their product from the market in 2016.
The majority of surgical mesh devices currently available for use are constructed from. Physiomesh is a patch used to strengthen the abdominal wall in hernia repair surgeries. Food and drug administration blamed recalled mesh for some of the worst complications. Manufacturers recalled the hernia mesh after people reported failures and organ injuries following surgery.
Bards ventralex st mesh was the subject of two class ii recalls in 2011. One of the first hernia mesh implants to be recalled was c. Apr 22, 2020 hernia mesh lawsuit attorney neil shouse explains the symptoms a patient may be experiencing if their hernia mesh implant has failed. Some canadian hernia surgery patients have launched a classaction lawsuit against the maker of a nowrecalled surgical mesh, claiming they werent warned of its dangers. Here are some of the hernia mesh recalls since 2005. These products are on the list because there is a reasonable chance that they could cause serious health problems or death. Despite the recalls, some people who underwent mesh hernia repair. Ventralex hernia patch is a selfexpanding, nonabsorbable, sterile prosthesis. However, mesh lawsuits continue to mount against the product. If you had a hernia repair procedure that used defective mesh, you could receive compensation. Hernia mesh lawsuit recalls, hernia repair complications. Bard, manufacturer of the defective kugel mesh hernia patch, has received an 11page warning letter from the us fda. The kugel mesh patch was approved for use by the u.
The mesh helps to strengthen that weak spot and hold the tissue in, but some brands of mesh have been recalled over very serious issues and complications. The damages you might recover in this type of case will depend greatly on the details of your case. Some were recalled by the food and drug administration fda, although most were voluntarily recalled by the hernia mesh. Bard received reports that the kugel patch was failing as early as 2002. Canadian patients join classaction suit over recalled hernia. Gore hernia mesh lawsuit johnson becker hernia mesh. The kugel patch was a line of hernia mesh products bard davol manufactured starting in the 1990s. Biological hernia mesh is derived from animal tissue usually cow or pig skin or intestine that is disinfected before it is.
Mesh is the preferred repair as it is supposed to minimize the possibility for infections and pain. The fda blamed recalled mesh for complications people reported to the agency. Bard announced the recalls after it became known that certain. Unfortunately, thousands of patients had already felt the impact of these complications by the time the product was recalled. A recalled bard hernia mesh patch allegedly caused a tennessee woman to suffer an infection, bowel perforation and other injuries that resulted in the need for multiple revision surgeries. One of the first hernia mesh implants to be recalled, the composix kugel has been the subject of three recalls in. Hernia mesh recalls have been issued over a number of brands of this surgical mesh over potential serious complications after surgery. Hernias occur when underlying tissue or organs squeeze through weak spots in the abdominal wall. Kugel mesh hernia patch lawsuit information do i have a. The sepramesh patch is not currently under fda recall. Hernia mesh products can be made from biological or synthetic materials. Some were recalled by the food and drug administration fda, although most were voluntarily recalled by the hernia mesh manufacturers after several patients reported injuries from having hernia mesh.
It was approved in the 1990s and has been implanted over a million times. A hernia mesh lawsuit is a claim against the mesh manufacturer by a patient who suffered complications and injuries as a result of mesh failure the lawsuits allege that the implant devices. The kugel patch contains a memory recoil ring around the perimeter of the mesh, which allows the doctor to fold it during the hernia repair. The schmidt firm, pllc is currently accepting ethicon physiomesh, atrium cqur mesh, and other hernia mesh injury cases in all 50 states. The fda issues recall of atrium medical corporations cqur vpack. Some settlements have reached several million dollars. But the company waited almost three years before recalling its mesh. Paul street suite 700, dallas, tx 75201 who associates. Canadian patients join classaction suit over recalled.
One of the first surgical meshes to be recalled was the kugel hernia mesh, manufactured by c. Our team of attorneys have successfully pursued hundreds of defective and recalled hernia mesh claims. Hernia mesh patch recall lawsuit the rothenberg law firm llp. In recent years, lawsuits were filed after ethicon pulled physiomesh off the market. The table below provides the hernia mesh recall list updated for 2019. It is designed to spring open once in place to lay flat. Hernia mesh manufacturers recall their products if they discover a problem. Console and associates has 25 years of experience handling. Hernia mesh is a simple medical device that is used to repair hernias, which occur when intestines or other tissue protrude through weak areas of muscle. Some of the most common symptoms of a failed device are burning sensations, bulging in the abdomen caused by an infection, feeling tired all day long, have sexual problems in the bedroom such as impotence, constipation and other digestion issues, feeling sick to.
Dozens of defective hernia mesh medical devices have been recalled. Jun 05, 2012 6 reasons why ri is best place to file a hernia mesh lawsuit against bard davol. Surgical mesh is a medical device that is used to provide additional support to weakened or damaged tissue. A hernia patch is a flattened material meant to prevent a hernia from pushing through the weakened muscle or tissue. Summaries of information about the most serious medical device recalls. Cqur vpack mesh made by atrium medical corporation was. Hernia mesh product recalls hernia mesh lawsuit in canada. Hernia mesh product recalls hernia mesh products can be made from biological or synthetic materials. Many complications related to hernia repair with surgical mesh. On january 24 th, 2007, the food and drug administration fda made national front page news after announcing plans to expand the recall of bard composix kugel mesh patch or bck patch to include more productlot numbers. Bard hernia mesh lawsuit alleges failure to warn about risks. A majority of these claims were still pending in 2018, when more mesh recalls were announced.
While surgeons may be told to stop using a specific type of patch, it is unlikely that any recall notice or warning letter would be sent to individuals who received the hernia mesh, and they may not learn about the recall or design problems with their patch until after severe complications have already been. The wellknow hernia mesh patch has received several recalls on their product leading to users filing lawsuits against the manufacturer of these. Bard hernia mesh lawsuit alleges failure to warn about. Mesh lawsuits for kugel hernia mesh recall saunders.
A ventralex hernia mesh lawsuit may be an option for hernia repair patients who suffered severe complications associated with the devices after hernia repair surgery. Jan 29, 2012 the wellknow hernia mesh patch has received several recalls on their product leading to users filing lawsuits against the manufacturer of these products. This patch however was recalled by bard as a result of reports of various. Hernia mesh lawsuits stem from device complications like infection, pain. Hernia mesh recall list what you should know 2019 update. Here is a timeline of the kugel mesh patch recalls. Hernia mesh patch recall the rothenberg law firm llp. Barddavol settled 3,000 lawsuits over recalled kugel mesh patch. This synthetic mesh is designed for use in hernia repair surgeries. Hernia mesh manufacturers have recalled more than 211,000 units of hernia mesh from 2005 to march 2018. May 22, 2017 a recalled bard hernia mesh patch allegedly caused a tennessee woman to suffer an infection, bowel perforation and other injuries that resulted in the need for multiple revision surgeries. Bard faced a class action lawsuit against the kugel hernia mesh patch, which led to the company paying out hundreds of millions of dollars in settlements. Hernia mesh manufacturers recalled more than 211,000 units of hernia mesh from 2005 to march 2018 at least. Hernia mesh lawsuits and settlements following recalls patients who suffered hernia mesh injuries are suing mesh manufacturers.
Many hernia mesh products, including some of those marketed by ethicon, atrium medical, and c. A common type of hernia mesh comes in the form of a patch or a plug. Most hernia mesh recalls have been designated with class ii status. Bard, issued eight recalls for various hernia mesh models between 2006 and 2007 alone. The manufacturer of the popular kugel hernia mesh patch, c. Filing a hernia mesh lawsuit may be an option for patients who experienced severe complications, including hernia recurrence and the need for revision surgery, following implantation of hernia mesh patches marketed by ethicon, inc. Our law firm is accepting clients who received a hernia mesh and have experienced additional surgeries, infections, bowel obstruction, organ damage, and chronic pain. Lawsuits have been filed by victims of ethicon physiomesh, atrium cqur mesh, c. Bard was subject to recalls for composix kugel mesh products due to safety concerns about the plastic which would splinter and migrate away from the surgical site. Bard and davol recalled composix kugel mesh products from the market starting in 2005. The recall, issued by the food and drug administration fda was a class 1 recall, the highest level of concern and had to be issued twice in 2005 and 2007.