Patients affected by the hernia mesh recall continue to look at their legal options including filing a Kugel patch lawsuit. The Kugel hernia mesh is a repair patch that was designed for use in open ventral hernia repair. It works by helping to eliminate the tension and strain on the surrounding muscles, which reduces discomfort after hernia surgery. A hernia is described as a weakness in the lining of the abdominal or pelvic wall. Specifically, the Kugel hernia patch is meant to repair the abdominal wall, effectively reinforcing any weak tissue that surrounds the hernia.

Surgeons make a small incision and create a pocket in the perperitoneal space. The hernia mesh patch will then be placed behind the hernia inside the abdominal cavity. A plastic memory recoil ring holds the patch in place, which allows the patch to folded during insertion and lay flat once it is in place. Over 78,000 hernia surgeries have used the Kugel hernia mesh patch.

Complications with the Kugel Hernia Mesh

Davol, the manufacturer of the Kugel hernia patch, began receiving complaints about the Kugel mesh patch in February of 2003. Apparently, the recoil ring that keeps the patch open after implantation is subject to break under the stress in the abdomen. The memory ring is a hard plastic that can form sharp edges, which can then puncture the internal organs.

Several cases have stated serious injuries, including bowel obstruction, bowel perforation, chronic intestinal fistulae, and serious infections. The symptoms of the Kugel hernia mesh breakage are said to be unexplained and persistent abdominal pain, fever, and tenderness at the site of the surgery. The manufacturing company began recalling the Kugel mesh patches in December of 2005, while also distributing patches that were meant to be larger and improved.

Hernia Mesh Lawsuit

The hernia mesh lawsuit has a goal of helping the individuals that have experienced illness or injury due to the Kugel mesh patch. If you have suffered any of the side effects from one of these defective hernia repair patches, then there may be legal recourse for you. You should confirm with your surgeon or physician that one of the recalled patches was used before seeking legal counsel, however. There is no nationwide class action suit against Devol for the defective Kugel hernia mesh, so each individual patient must seek damages on their own.

The pending lawsuits state that Davol should be held responsible, as it is the duty of any pharmaceutical and medical device company to provide the consuming public with safe and tested products. Many patients are suing for unpaid medical bills, lost wages, pain and suffering, and a loss of their quality of life. Family members of those that have died as a result of the hernia mesh recall are seeking damages for pain and suffering, as well as any remaining medical bills. If you think there is a chance that you are the recipient of one of the defective Kugel hernia mesh patches, then you should see your doctor right away.

Kugel hernia patch litigation is currently ongoing and some claimants that filed early cases have been able to receive Kugel mesh settlement amounts. Though it may not seem like it at first glance, suffering with a hernia can be an extremely painful and debilitating medical condition. Medical science has provided all manner of treatments and procedures designed to alleviate the symptoms (and the hernia itself). Everything from lasers to medications to invasive surgery is routinely employed to treat all types of hernias.

In recent years, a new type of treatment was developed by a doctor named Robert Kugel. The treatment was the Kugel hernia mesh implant. This patch is surgically inserted into a patient’s inner abdominal cavity, where it repairs the abdominal wall following the surgical removal of a hernia. The hernia mesh implant is placed in parts of the inner abdominal wall where scar tissue has weakened the inner lining of the abdominal cavity.

To understand how the Kugel hernia mesh implant is causing adverse side effects, it helps to have a little background on hernias and hernia treatments. L

What Is A Hernia?

A hernia is a tear or a weak spot in the muscular tissue of the inner wall of a patient’s abdomen. Any such tear or weakness results in a peculiar bulge protruding on the inside of the abdominal wall, and can make everyday activities extremely painful. These activities include anything that causes compression or extension of the abdominal cavity, such as coughing hard, lifting, bending, and any number of natural biological processes.

What Is A Hernia Mesh Implant?

Dr. Robert Kugel developed the hernia mesh implant as a way to treat patients who have had a hernia surgically removed. The hernia mesh implant is grafted onto the weak spots or tears left behind following a hernia’s removal, in order to make the affected area strong, and to allow the area to heal properly.

The Kugel hernia mesh implant was manufactured and distributed by the company Davol, Inc., and is often referred to as the Bard Composix hernia patch. The mesh hernia patch is made of a polypropylene dual layer material that centers around an outer memory recoil ring.

Why Were The Kugel Mesh Implants Recalled?

It is alleged that the Kugel hernia mesh patch has a defective outer memory recoil ring that can split, tear or rupture if the inner abdominal cavity is compressed or extended during physically demanding endeavors. Also, there are many reports of extensive and dangerous side effects related to the Kugel hernia mesh implants, leading to the hernia mesh recall in 2005.

What Are The Side Effects Of Hernia Mesh Implants?

One reported “side effect” of a failure of the Kugel hernia mesh implant is bowel perforation caused by sharp or frayed edges of the mesh puncturing or slicing into nearby internal organs. For many patients, the onset of different kinds of infections following the implant surgery also occurs. Most of these hernia mesh side effects require immediate surgery to repair and to extract the mesh patch before it does any further damage to internal organs. In some cases, the Kugel mesh side effects are permanent, and cannot be repaired by surgery or medical treatment. If you have suffered from complications due to defective mesh, you are encouraged to investigate your legal rights including filing a hernia patch lawsuit. There is a limited time to file claims based on statute of limitations that apply to your case.

From improved and medical device technology to a veritable golden age of surgical innovation, it seems as though the sky is the limit as far as the possibilities of our technological innovation go. However, there are always setbacks. In fact, given the current state of modern medicine it is often hard for regulators to keep up with all of the advancements and new products which can lead to defective products entering the marketplace. This is often followed by a host of recalls and lawsuits announced in the wake of many high profile problems with leading medications and treatments. One of these defective products was involved in the Kugel mesh recall.

With the recent hernia mesh recall, it seems that a once promising new product has turned out to be linked with serious complications and significant side effects that can be incredibly debilitating. One more “innovation” can be added to this list. Davol, Inc., the makers of the Bard Composix hernia mesh patch, is currently facing lawsuits from thousands of litigants regarding a major defective flaw in their hernia mesh implants.

How the Hernia Mesh Implant Works

Dr. Robert Kugel developed a mesh patch designed specifically for patients who had recently had a hernia removed from the interior of their abdominal wall. When a hernia is surgically removed, there is significant build up of scar tissue, and parts of the inner abdominal wall are extremely weak. Kugel’s mesh patch is surgically grafted into the abdominal wall where a hernia was removed, to help shore up the inner lining of the abdomen, and to allow the area to heal quickly.

The Different Types of Hernias

Hernias basically come in four main types. There is the direct hernia, which is a hernia that juts out from a tear in the wall of the interior abdominal cavity. Indirect hernias are ones that do not protrude completely. Femoral hernias are hernias that protrude into the intestines due to an extreme failure of the inner abdominal wall, and ventral hernias are found in the upper part of the abdominal cavity. Ventral hernias are often not painful, and are only revealed while treating more immediately painful hernias.

Hernia Mesh Infections and Other Hernia Mesh Complications

The mesh patch is comprised of a center memory recoil ring that, once placed into the interior wall of the abdomen, snaps the mesh into place. The problem for Davol, Inc., is that these memory recoil rings were defective. They were prone to rupturing inside the abdominal cavities of patients when the abdomen was compressed or extended, such as during most types of physical exertion.

When the hernia mesh patches rupture, they send jagged and sharp pieces of the mesh implant jutting out into the interior of the abdominal cavity, which threatens nearby internal organs. The most common complication from the mesh implants is the perforation of the bowels by a jagged piece of the implant. Often, these punctures and perforations cause severe septic infections. It was the defective recoil rings that prompted Davol to issue a hernia mesh recall of all of the Kugel patches. Please contact us for the latest Kugel mesh settlement information and updates.

Though considered a non-life threatening ailment, a hernia can be a severely limiting and painful medical condition to endure. It affects nearly every waking movement you make, and can present a serious problem for a host of involuntary biological processes every day until it is treated. Complicating matters is the fact that the only way to treat a hernia is to remove it, and the only way to do that is through surgery. Some hernias can be removed with a laser, but many (most, in fact) still cannot be without jeopardizing internal organs. Patients affected by defective Kugel mesh continue to file a hernia patch lawsuit to help with outstanding medical bills and long-term injuries. Please contact us for the latest news updates.

One of the ultimate problems with hernia surgery is that it leaves parts of a patient’s inner abdominal wall extremely weak, and covered with scar tissue. Realizing this, Dr. Robert Kugel developed the Kugel hernia mesh patch implant that was produced and distributed by Davol, Inc., under the trade name Bard Composix Hernia Mesh Patch. At the time it was released, this hernia patch seemed to be a good solution, helping patients heal from hernia surgeries quickly and with little inner abdominal pain.

What Are The Different Types Of Hernias?

There are four main types of hernias – direct, indirect, femoral and ventral hernias. The type often depends greatly on the location of the hernia. Direct, indirect and femoral hernias are most commonly found in the groin area, while ventral hernias are found primary in the upper abdominal cavity, along the interior wall of the abdomen.

How the Kugel Hernia Mesh Patch Worked

The Kugel hernia mesh patch is a dual layer composite propylene material that is grafted to the areas of the inner abdominal wall that are weakened by the removal of a hernia. The mesh patch is used to help strengthen the inner abdominal wall, and to facilitate healing of the inner abdominal tissues that line the wall.

Why the Kugel Mesh Recall Happened

Davol recalled tens of thousands of the hernia mesh implants due to the severe nature of the many side effects and complications that occurred. These major failings revealed that a crucial component of the Kugel mesh patch was defective. At the center of the patch is an outer memory recoil ring. What happens for many patients is that, when the inner abdominal cavity is placed under rather ordinary stress, the recoil ring suffers failure, and splits apart. This leaves sharp, jagged edges of the mesh material jutting out into the abdominal cavity.

The Dangerous Side Effects Resulting From Kugel Mesh Complications

What happens when the center recoil ring of the Kugel hernia mesh implant fails, and ruptures, is that it can puncture or perforate any of the nearby internal organs. Since the mesh implant is commonly placed adjacent to the many organs in the lower abdomen, any puncture or perforation can damage the bowels, intestines, or any of the other organs nearby. This can, obviously, cause severe health problems. Patients who have had a Kugel mesh failure are often operated upon immediately to prevent serious complications with their health. If you or a family member has suffered injuries due to defective Kugel mesh please contact us for a free consultation regarding your legal rights and the latest news updates for a hernia mesh lawsuit.

Following patient complaints of hernia mesh problems certain lots of the Kugel patch was recalled in 2005. A hernia is described as a weakening of the walls in the abdomen or the pelvic area. These can be painful to the patient that suffers them, so Davol, a medical device company, developed the Kugel hernia mesh patch to aid in healing after hernia surgery. The Kugel hernia patch is inserted through a small incision in the abdomen and then placed into a pocket in the perperitoneal space.

The hernia patch includes a plastic memory recoil ring that holds the patch in place between the abdominal wall and the hernia. The Kugel hernia mesh patch can be folded before insertion, and then the memory coil springs open so that the Kugel patch will stay in place. Once the patch is in place, the Kugel hernia mesh patch works to reduce discomfort after the hernia surgery. It is estimated that over 78,000 hernia patients have the Kugel hernia mesh patch.

The Kugel Hernia Mesh Presents Complications

In 2003, patients began complaining to Davol, the makers of the Kugel hernia mesh patch. The recoil ring that was meant to keep the patch open after insertion is prone to breaking under the stress of the abdominal muscles. Because the patch is made with hard plastic edges, the broken patches formed sharp points that could puncture the internal organs.

The resulting illness and injuries included bowel perforation, serious infection, chronic intestinal fistulae, and bowel obstruction. The symptoms of these injuries were described as persistent abdominal pain, fever, tenderness at the site of the surgery, and nausea or vomiting. When left untreated, these conditions have led to death. As a result of these complaints, Davol began a hernia mesh recall of the defective Kugel mesh patches in December of 2005 and began distributing patches that were improved.

Kugel Mesh Patch Lawsuits

Many believe that Davol should be held responsible for the illness and injury that many of the Kugel hernia mesh patch patients have experienced. It is important that pharmaceutical and medical device companies are held accountable for the medical products that they distribute. Patients that have experienced the side effects, illnesses, or injuries can seek legal damages through a lawsuit against Davol. There are no current class action lawsuits pending, but many individuals have opened their own cases against the medical device company which have been consolidated into what is referred to as multi-district litigation (MDL).

The lawsuits basically state that Davol did not fully disclose any possible side effects or malfunction of the Kugel hernia mesh patch and that there was not adequate testing performed on the hernia patches before they were distributed for use in hernia surgeries. The claimants are seeking damages for medical bills, lost wages, loss of independence and quality of life, and pain and suffering. Many patients have had to undergo hernia mesh removal surgery. Those that have lost family members due to complications with the Kugel hernia mesh are suing for any remaining medical bills, as well as for pain and suffering. It is important to check the statute of limitations for that state in which the lawsuit will take place, because each state has individual requirements. Claimants should also consult their doctor to ascertain that they do, indeed, have the Kugel hernia patch.

Hernia mesh complications have required the manufacturer of some of the most widely used hernia repair patches, Davol, Inc., to recall several lots of their products. The hernia patch recall has been one of a series of manufacturer recalls that have taken place since the end of 2005. These recalls affect several other products made by the same manufacturer, as well, and were brought about by significant complaints about the safety of these products.

Understanding the Hernia Mesh Recall Actions

The Kugel mesh was recalled due to numerous different issues. Some of the Kugel mesh complications, and the problems with other devices by this manufacturer, had to do with patients having reactions to the materials from which the patches were made. Other cases involved parts of the device breaking, such as the ring that constitutes a major part of its structure. Ring breakage has caused several injuries to patients, including perforated bowels and bowel obstructions, which have both been significant reasons that hernia mesh recall actions have been taken.

How Hernia Mesh Problems Arise

The most common type of hernia is an abdominal hernia. These conditions constitute weakening of the abdominal and pelvic walls and are associated with exertion and age. The Kugel mesh complications that have led to so many recalls have to do with the way these devices do their job. At the simplest level, a Kugel mesh patch is a ring with a polypropylene mesh attached to it. It is named for the doctor who designed it and it provides support to weakened areas of the anatomy by reinforcing weakened and torn tissues.

The hernia mesh complications that affect most patients arise when the metal ring that provides the frame for the mesh breaks. This results in the sharp edge of the ring being exposed. This can lead to complications including bowel perforations, hernia mesh infection and others that are very serious and which require medical intervention.

There are several different patches that have been recalled since 2005. They include the extra large patches. Hernia repair mesh recall actions have also been taken for Bard, Composix and Kugel brand-name products. If you have such a device, you were likely notified by mail of the hazards associated with your product. The company sent notifications via FedEx on the occasions when the hernia mesh recall had to be undertaken.

Who Is Affected by the Hernia Mesh Patch Recall?

There are over 600,000 hernia operations performed annually. There are few other treatments for this condition and, because of that, the patients have little recourse but to hope for the best from this radical intervention. If you have a hernia patch, you may be at risk for hernia mesh complications.

If you’ve received notice that the hernia mesh patch recall affects you, you can contact a lawyer. You may have a case to file a hernia mesh lawsuit due to your injuries. If you have one of these patches and are concerned, consult with your doctor and then, if needed, with an attorney who can explain your legal rights and discuss the latest information regarding Kugel mesh settlement amounts.

If you have a painful protrusion in your abdominal area that seems to expand when you cough or strain to lift a weight, you may have an abdominal hernia. In the last several years there has been a hernia mesh recall of certain types of hernia patch repairs. Attorneys are currently looking at a Kugel mesh settlement for their clients and claims are being filed individually rather than in a national hernia mesh class action.

A hernia occurs when an organ pushes through a weak muscle wall or area of tissue. In the case of abdominal hernias, part of the intestine can push through the stomach wall, creating a bulge.

For most people, the hernia is caused by an inherent weakness in the muscle, coupled with something that puts stress on that area. Obesity, pregnancy, heavy weightlifting, excessive coughing and straining during bowel movements can provide enough force that a hernia develops in a vulnerable area. Hernias may also develop at incision sites from previous surgeries.

Hernias may exist without being noticed, and they may not cause any problems, but for many people, hernias can cause pain. When this happens, a doctor may recommend surgery to repair the weak area.

In this surgery, called a hernioplasty, doctors may insert a patch of material over the weakened area. This mesh material can remain in the body and bolsters up the muscle or tissue to keep the organ from bulging through.

An untreated hernia can lead to complications. If an organ, like the intestine, pushes through the stomach wall, it can become trapped there and its blood supply can be cut off. Without oxygen and blood, that organ will develop tissue damage. In extreme cases, gangrene may occur, and the gangrenous area would have to be removed.

Although treating a hernia through surgery is standard practice, even this relatively simple procedure can have risks.

In recent years, some patients have had hernia mesh problems due to a malfunction in a part of the Bard Composix Kugel Hernia Patch. With the Kugel patch, a plastic ring that connected the two pieces of mesh would sometimes break, and the sharp edges from the ring could puncture internal organs, causing serious complications.

One complication is a perforated bowel, in which the ring creates a hole in the stomach or intestine and food from one of those organs leaks into the abdominal cavity, causing a potentially life-threatening infection. Another complication is a fistula, which is an abnormal connection or passageway between two parts of the intestine. This can cause both pain and infection. Over 80 injuries and problems have been reported as a result of broken rings, including several fatalities.

Although the Kugel patch has been recalled and revised patches have been developed, patients are advised to leave functioning patches in place until or unless a problem arises.

If you or someone you know is affected by the Kugel hernia mesh recall, you may have important legal rights. Perhaps you have had hernia surgery, but are unsure of whether or not you received the Kugel patch. There is a limited time to file a hernia patch lawsuit.

Several Kugel mesh recall announcements have been issued because of injuries caused by the Kugel products.

What does the Kugel mesh patch do?
Kugel Mesh was introduced to the market by Davol Inc. The Kugel mesh patch is used to repair ventral (incisional) hernias caused by thinning or stretching of scar tissue that forms after surgery. The patch is placed behind the hernia defect through a small incision. The patch is then held open by a “memory recoil ring” that allows the patch to be folded for insertion and later spring open and lay flat once it is in place. The FDA approved the patch in 1996. In 2002, problems began to surface.

What recalls have been issued?
On December 22, 2005, Davol, Inc. recalled its extra large Kugel mesh patch. In March 2006, the recall was expanded. The lots manufactured prior to January 2004 were recalled during the March 2006 expansion. Since the March 2006 recall expansion, Davol received four confirmed complaints of recoil ring breakage from one of their product codes manufactured between January 2004 and September 2005.

Davol notified U.S. customers of the initial hernia patch recall by letter on December 27, 2005, which it sent via Federal Express. On March 24, 2006, Bard issued letters to hospitals and health care professionals alerting them to the additional recalled products. The letters included updated Instructions for Use (“IFU”) clarifying the proper insertion technique and Supplemental Patient Management Information.

On January 10, 2007, Davol, Inc. issued another Kugel hernia patch recall for patches that were manufactured before October 2005. Davol sent letters to health care professionals and distributors notifying them of the most recent expansion of this recall of specific lots Kugel mesh patches. The letter stated that surgeons and hospitals should stop using the recalled product and return unused units to the company.

It should be noted that Davol also decided to withdraw from the market specific lots of mesh patches that were manufactured from October 2005 to October 2006. A market withdrawal is a company’s removal or correction of a distributed product that would not be subject to legal action by the FDA.

Why was the Kugel mesh patch recalled?
The reason for the Kugel mesh recall is that the “memory recoil ring” that opens the patch can break under the stress of placement of the large sized products in the intra-abdominal (inside the belly area) space. This can lead to bowel perforations (rupture) and/or chronic (recurring) intestinal fistulae (abnormal connections or passageways between the intestines and other organs).

When should you seek medical attention?
The FDA recommends that patients who have been implanted with one of the recalled devices seek medical attention immediately if they experience symptoms that could be associated with ring breakage such as unexplained or persistent abdominal pain, fever, tenderness at the implant site or other unusual symptoms. If you have any questions regarding your legal options, including filing a Kugel mesh lawsuit, please contact us for a free no-obligation consultation.

Patients suffering from hernia mesh problems continue to look at their legal options including filing a hernia mesh lawsuit. The Kugel mesh hernia patch was made available to the market in order to aid the healing process of a hernia surgery. Many believed this product ever since it came out. But after this patch was implanted to numerous of patients, many complained about extreme abdominal pains. Once the FDA found out about this, they announced a hernia mesh recall of this product which was followed by consumers who filed a Kugel mesh lawsuit. This is certainly a serious matter because there are many lives that were put in danger. They thought everything would bring back their normal state once they use this kind of patch but the result turned unfavorable to them.

What is a hernia? A hernia occurs when a part of an internal organ commonly the intestine or colon protrudes through a weak muscle or membrane that holds the abdominal organ in place. There are several kinds of hernia namely inguinal, incisional, umbilical, and femoral hernia. Before the patch recall was announced, thousands of kugel hernia mesh patches were implanted in patients throughout the United States.

The Kugel mesh patch was supposed to help patients with hernia. This medical innovation was hailed by doctors everywhere. But it was not until problems regarding the product started to arise. Many people were involved including the companies which produces it. The mesh hernia patch was found to be a harmful medical product and this called for major actions from the involved parties. Lawsuits have been filed by patients who have suffered complications following surgery.

In recent years, the FDA announced a Kugel mesh recall after discovering that the plastic ring that connects the mesh patch was prone to breaking. When this happened, the hard plastic break point of the ring could puncture internal organs. Patients experienced side effects including perforated bowels and chronic fistulas. To date, more than 80 people have had injuries, including death, as a result of complications from the Kugel patch.

Reports indicate that the Kugel patch manufacturer, Davol, Inc., a subsidiary of C.R. Bard Inc., was aware of defects with the ring, but may not have tracked them effectively or addressed them immediately.

As a result of the complications caused by the defective device, affected patients have initiated a hernia mesh lawsuit seeking compensation. If you have had surgery to repair a ventral hernia in the last five to eight years, you may be included in this group.

Hernia patients coming forward with obvious side effects made the Kugel patch recall successful. The risks involved before the said recall were notable. Death is the most distinguished danger the patch has brought to hernia patients. Possible complications like bowel perforation, bowel obstruction, and intestinal fistula could add up to the list. Those who have received this patch may have experienced unexplained, persistent abdominal pain, fever, tenderness to the implant site, nausea, and vomiting.

The FDA or the Food and Drug Administration had spearheaded the spread of information regarding the Kugel mesh hernia patch. The Kugel patch recall has been done before more patients became at risk for the bad effects of the hernia patch. The FDA urged many patients who receive the Kugel patch to seek immediate medical attention because of the products indicated malfunctions. Patients were advised to see a doctor whether the patch should replaced or removed. This recall issued by the FDA was classified as class 1 recall making it as one of the most serious recalls.

What is Kugel Mesh?
A hernia mesh lawsuit can be a person’s only way to seek legal justice for harm caused by complications caused by a defective Kugel Mesh patch. Kugel Mesh is a patch designed to make hernia operations easier and reduce post-surgical pain for patients. The FDA approved the patch in 1996. The Kugel Mesh patch consists of two layers of synthetic mesh surrounded by a flexible plastic “memory recoil ring.” It is implanted at the site of a hernia. The “ring” then springs into place, which allows the hernia to heal and re-grow around the patch. Kugel Mesh was introduced to the market by Davol Inc. In 2002, problems began to surface.

What problems are associated with Kugel Mesh?
In some cases, the ring in the Kugel Mesh patch has broken. This has caused severe injuries to patients’ internal organs and tissue, including bowel obstructions, bowel perforations, and chronic enteric fistulas. Davol initially blamed the surgeons who installed the Kugel Mesh patch for the broken rings. Davol claimed that the doctors made mistakes which caused the breaks in the rings. However, tests conducted by Davol revealed that the failure almost always occurred at the spot where the ring was welded together, which was done by the company.

What has the FDA done?
In the early part of 2006, the FDA inspected Davol’s manufacturing plant. The FDA found major problems in the system for tracking and reporting patients’ complaints about the Kugel Mesh side effects. The FDA concluded that Davol had been downplaying the severity of the injuries associated with the Kugel Mesh patch, including that one person may have died from this product. These findings by the FDA prompted two recalls.

Kugel Mesh Recalls
Davol issued a Kugel hernia patch recall in December 2005 for the extra large model of the Kugel Mesh patch. This came as a result of Davol’s tests that uncovered the design and manufacturing flaws. Davol issued two more recalls for its Kugel Mesh hernia patches in March 2006 and January 2007, at the prompting of the FDA after reports linked the hernia patch to more than 80 injuries and several fatalities.

Where would we file the lawsuit?
Where a Kugel Mesh lawsuit can be filed depends on a number of factors. The first lawsuit was filed in Rhode Island in December 2006. Since then, many other hernia mesh lawsuits have been filed. Attorneys representing victims of the Kugel Mesh product allege that their clients have suffered pain and were required to undergo bowel dissection surgery. If you have experienced any Kugel Mesh side effects or complications, you should contact an experienced Kugel Mesh lawsuit attorney to discuss your legal options.