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Are you or a loved one experiencing complications due to a hernia mesh implant or procedure? People are starting to speak up and are filing claims against their injuries. It’s time to take action. You may be entitled to financial compensation. Get the Answers you need.


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Complications due to the Hernia Mesh Recall

Trends are appearing and here are some common problems from some plaintiffs.


In the FDA’s analysis of medical adverse event reports to the FDA, recalled products were the main cause of bowel perforation and obstruction complications.

Return of the Hernia

Hernia recurrence is the most common complication of hernia operations. This is caused by improper surgical technique, shrinkage, movement or migration of the device.


Some hernia infections can be treated with acute antibiotics. Sometimes it requires the removal of the device and other solutions are used for repairing the hernia.


An adhesion is a band of scar tissue that binds two parts of tissue or organs together. Adhesions may appear as thin sheets of tissue similar to plastic wrap or as thick fibrous bands.

Intestinal Complications

Placed inside the abdominal cavity, the device may become stuck to part of the bowel. In some cases, they can kink the intestine and cause a blockage.

Recurring Pain

Moderate to severe pain that persists after hernia surgery, especially if "searing" or "electric" feeling, may be a sign of nerve entrapment. This is caused by either the device or the sutures or staples.


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About the Hernia Mesh

These hernia repair devices are typically used in various capacities and is often times cut specifically to the size of the patients needs. Multiple forms of repair techniques are used in the procedures. The device is inserted into the patient in one of two ways. It is placed either under … or … over the hernia or other variations and is held in place by some simple stitches. The material on the hernia acts as a kind of roadmap for the new growth of a patient’s own tissue. The hernia device will eventually incorporate into the surrounding area and will have to be removed or dissolve. We have plenty of more information for you to utilize and the answers you are looking for so be sure to visit our about page.

Hernia Mesh Recall 3
Hernia Mesh Recall 3

What's This About A Recall?

If you have been completely in the dark about the work about defective hernia repair products out there, then this is your chance to get caught up. We have an excellent blog about recent happenings to keep you informed. But, lets talk about the largest developments. In April of 2010, the FDA urged patients to determine if they have a Bard Composix Kugel Patch. The U.S. Food and Drug Administration recently issued a "Class 1" recall of these hernia repair patches because the defect associated with the use or exposure to the Kugel Hernia Patch has a reasonable probability to cause serious adverse health consequences, including death, according to the FDA. Patients can view a complete list of the patches in the recall by contacting us here and we will determine if you or your loved one had received one of these problematic patches. If you would like to lean more about recalls, be sure to head over to our page with more information.

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