Composix Hernia Patch Recall

When it came out on the market the Composix patch was deemed to be an innovative and effective way of assisting in the repair of abdominal hernias. The belief was that with the Composix patch a person would be able to obtain hernia repair in a shorter amount of time, a repair of the hernia that would be lasting and effective. However, by 2007, over 100,000 Composix patch units had been recalled. Through this article you are provided an overview of information relating to the Composix patch recall. Armed with this information you will be in the best possible position to know what steps that you need to take in order to protect your rights and interests should you have found yourself involved in a Composix patch recall.

In regard to the Composix patch recall, there is one primary defect associated with the product. Specfically, the Composix patch contains a ring. Specifically, this is known as the memory recoil ring and is responsible for opening the Composix patch itself once it is placed into a person’s abdomen.

At the time of the Composix patch recall, the Food and Drug Administration or FDA received reports of ring breakage. Some patients experienced very significant injuries as the result of the ring breakage. Additionally, deaths have been associated with the ring breakage as well.

When the Composix patch fails because of the memory recoil ring breaking inside a person’s abdomen, a number of serious injuries potentially can occur.

These injuries and damages (which gave rise to the Composix patch recall) include:

• sepsis
• bowel obstruction
• abnormal connection between organs that do not normally connect
• ring migration through the abdominal wall
• perforation of the intestines

These different injuries tend to be extremely painful and can cause permanent damage to an individual. You may have chronic problems that last well into the future if not for the rest of your natural life. Moreover, correcting and resolving some of these issues can require what amounts to serious surgical procedures.

As was also noted, there have been reports of individuals who appear to have died as the result of the defect that is the subject of the Composix patch recall. Therefore, you may have a loved one who has died as a consequence of the defect discussed in this article.

If you are like many individuals who have suffered the negative side effects associated with the Composix patch defect, you will want to consider consulting with an attorney, with a lawyer who has the expertise necessary to assist in regard to matters relating to the Composix patch recall.

In searching for a lawyer, you definitely will want to focus your attention on those attorneys that specifically are experienced in regard to matters relating to the Composix patch recall. In the end, you definitely have a good deal riding on being able to obtain the compensation that you may be entitled as the result of suffering damages and injuries as the result of a defect in this product.

If you’ve been injured by the Composix Kugel Mesh Patch, please call an experienced hernia patch lawyer about your case by calling the McEwen Law Firm at (800) 732-3070 or by filling out our free case evaluation form to the right.

Kugel Mesh Hernia Patch Lawsuit

The Kugel Mesh Patch Recall has been recently announced due to the serious side effects they cause. These side effects result in extreme abdominal damage, additional surgery, and in some cases death.

Those suffering from Kugel mesh patch side effects experience extreme discomfort, may miss time from work, and may end up with thousands of dollars of medical bill debt. In the worst cases, families lose the lives of loved ones as a result of the use of these faulty patches.

Due to the life altering affects of Kugel Mesh patches, there is currently a class action lawsuit against the makers of the patch. For victims of the Kugel mesh hernia patch taking part in a class action lawsuit can mean compensation for their pain, damages, and economic losses.

Currently, McEwen Law Firm is taking part in the class action lawsuit against the makers of Kugel mesh patches. McEwen Law Firm hernia patch lawyers are dedicated to providing victims with the legal assistance they need to receive compensation for their losses.

To contact McEwen Law Firm for a free, no obligation, consultation today please call (800) 732-3070 or fill out our online contact form.

For more information visit Kugel Mesh Patch Lawsuit - our affiliate website.

Kugel Mesh Hernia Patch Side Effects

The Kugel mesh hernia patch has been recalled due to the serious side effects that have been linked directly to the patches. A nationwide Kugel Mesh Hernia Patch Recall has been recently announced. Kugel mesh patches are typically used after hernia surgery in the abdominal area.

Bard Composix Kugel mesh patches have been linked to:

• Chronic Fistuals
• Infection
• Bowel Obstructions
• Bowel Perforations

These conditions result in severe abdominal pain, additional surgery, and in some cases death.

Kugel mesh side effects are caused by the hernia patch’s recoil ring. The ring which is designed to open after implantation breaks under stress, causing the above side effects.

Side effects typically begin as severe abdominal pain and progress into more severe conditions as time passes. Those who have been given a Kugel mesh patch and experience severe pain should seek medical attention immediately.

If you or a loved one has suffered as a result of using Kugel mesh patches contact McEwen Law Firm today. Our Kugel mesh class action lawyers can help you get started on the right path for legal compensation as quickly and efficiently as possible.

To contact McEwen law Firm for free today call (800) 732-3070 or fill out our online contact form.

For more information visit our Kugel Patch Side Effects affiliate website.

Hernia Patch Recall List

McEwen Law Firm is a nationwide law firm representing product liability lawsuits with an emphasis on the Kugel Patch Recall Lawsuit. On January 8th, 2008, a Federal Court judge explained that hernia patch lawsuits will include the Davol & Bard and Marlex & Teflon patches that have and do not have the memory recoil rings.

If you or a loved one has received a recalled or defective Kugel Mesh Patch you may have suffered bowl perforation, bowl obstruction, chronic intestinal fistulae, or infections. You may be entitled to seek compensation. We can help. Call us today toll free at (800) 732-3070 for a free case evaluation.

Complications and failures of the hernia mesh patch have been known for many years now by the manufacturers and have gone underreported to the FDA. Side effects of the hernia patch include bowel obstruction, constipation, and fistula. Use of the Composix Kugel Mesh Patches have also included reports of the memory recoil ring breaking with signs such as the patch shriveling, the edges curling upwards, and a buckled mesh. The mesh has been described as wrinkled, crumpled, rolled up, and folded by those affected.

Breakage of the memory recoil ring that holds the Kugel Mesh patch in place causes the serious side effects of the medical device. Symptoms of ring breakage include:

• Abdominal pain or fever
• Tenderness at the implant site
• Persistent stomach pain

Below you will see the three seperate hernia patch recall information. These recalled medical devices and product codes show the manufacturing dates and product codes being recalled. If you have used a recalled or defective Kugel patch or suffered any of the side effects associated with the patch, you should seek out a medical professional and call the McEwen Law Office at (800) 732-3070.

Extra Large Oval, 8.7” x 10.7”
All Lot Numbers manufactured before January 2006
Product Codes: 0010206

Extra Large Oval, 10.8” x 13.7”
All Lot Numbers manufactured before January 2006
Product Codes: 0010207

Extra Large Oval, 7.7” x 9.7”
All Lot Numbers manufactured before January 2006
Product Codes: 0010208

Oval, 6.3” x 12.3”
All Lot Numbers manufactured before March 2006
Product Codes: 0010209

Large Oval, 5.4” x 7.0”
All Lot Numbers manufactured before October 2005 & also Including the following:
41L, 41M, 41N, 43L, 43M, 43N
Product Codes: 0010202

Large Circle, 4.5”
All Lot Numbers manufactured before October 2005 & also Including the following:
41L, 41M, 41N, 43L, 43M, 43*N
Product Codes: 0010204

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Bard Composix Kugel Mesh Patch Recall

Bard Composix Kugel mesh patches, a medical device used to treat hernias, were recalled in December 2005 due to serious side effects and complications.

Kugel mesh patch side effects include bowel obstructions, perforations, chronic fistulas, and infection. These side effects cause serious damage, may require additional surgeries to repair, and in some cases may cause death.

Bard Composix Kugel mesh patches came on to the market in 2002, and although a number of companies knew of problems with the patches, they were not recalled until 2005. The negligence of these companies caused many people across the United States to be injured by Kugel mesh patches.

If you or a loved one has suffered an injury from recalled Kugel mesh patches please contact McEwen Law Firm today. Our Kugel mesh patch lawyers are dedicated to providing victims and their families with the compensation they deserve after suffering life altering Kugel patch injuries. McEwen Law Firm attorneys are currently involved in the Kugel mesh class action lawsuit.

To contact McEwen Law Firm free of charge today please call (800) 732-3070 or fill out our online contact form.

For more information visit our Composix Kugel Mesh Recall affiliate website.

Hernia Patch Lawsuit

Patients who have been injured from using the Composix Kugel Mesh Patch have recently filed hernia patch lawsuits against the manufacturer, Davol Inc. and C.R. Bard Inc.

The Hernia Patch Class Action Lawsuit alleges that the two companies were manufacturing and designing problems that existed in the hernia patch and did not inform patients, doctors, or other medical professionals who were administering the Kugel Mesh Patch.

Davol has discovered that a memory recoil ring that surrounds the patch and holds it in place has a tendency to break in patients after being inserted. The breaking of the Kugel Mesh Patch has lead to several severe health problems including:

• Bowel Obstruction
• Bowel Perforation
• Chronic Enteric Fistulas

The FDA has found that the company, Davol, did not report properly to medical and health professionals of these findings or properly report complaints it had received about the breaking of these hernia patches.

After these reports were found by Davol the company did not inform the FDA and continued selling the defective hernia patch. After the December 2005 hernia patch recall, the company’s findings finally became well known. Hernia patch lawsuits have been filed against the makers of the hernia patch which accuse them of fraud, wrongful death, and negligence.

If you’ve been affected by the hernia patch recall you may be entitled to seek damages from a skilled lawyer at the McEwen Law Firm. Our lawyers are well aware of the hernia patch side effects and can help you recover your medical and other financial losses. Call us today toll-free at (800) 732-3070 for a free consultation regarding your case and possibilities.

For more information on the Hernia Patch Lawsuit please visit our affiliate website.