hernia mesh recall surgery

Surgical mesh in hernia operation

Hernia mesh is a medical device used in the implant surgery during hernia repair process. It helps to reinforce the weakened tissue and also prevent the recurrence of a hernia.

A brief understanding of the hernia meshes

Typically, any surgical mesh is made of synthetic materials or of animal tissues (pigs or cows). Synthetic meshes, which are commonly used in the recent decades, are woven of absorbable material, non-absorbable material or a combination of both these materials. This is because, medical studies have shown use of hernia mesh correlates with a decrease in the hernia recurrence rate. Unfortunately, some of the hernia meshes have caused an unreasonably high number of complications that led to recall of such products from the market.

As much as 90 percent of hernia repair surgeries in the U.S. use surgical mesh. Conventional hernia surgery stitches the tissues back together however, there have been some serious complications associated with them.

Complications that led to recall

Manufacturers such as Atrium, Ethicon, Bard, Medtronic has been some of the trusted names who actually concealed the probable complications associated with the meshes.

The major health complications include:

Fistula – The most serious concern with a defective hernia mesh is formation of fistula. is a late complication of prosthetic mesh repair that is caused mainly because of chronic erosion of bowel by the mesh particles placed in contact with the intestinal loops. Sudden discharge of pus or blood, irritation around the anal region, swelling, redness and tenderness in anus, pain associated with bowel movements and fever are some of the common symptoms.

hernia mesh recall surgery

Infection – to correct a faulty implanted surgical mesh, corrective surgeries are the only way out which is linked with causing infection. Also, the signs of infection may be clinically apparent many years after the implantation. The associated pain is not only because of using synthetic mesh but for the fact that the mesh is secured with stitches can become entangled with the nerves causing chronic pain.

Dental Problems- high rate of clients have complained about the teeth becoming weak, infected, chip off after the mesh infection.

Flu-Like Symptoms- nausea, chills, fever or vomiting are common complications post the hernia repair. For instance, the Atrium C-Qur hernia mesh is made with omega 3 fatty acid coating which often provokes an immune system response fighting the infection and the mesh.

What is recall and where are the surgical mesh placed?

A recall is basically a removal or correction of a medical device. The FDA designates a class corresponding to the degree of potential harm associated with the recall items. Basically, there are three types of classes of recalls such as:

  • Class I FDA Recall

This represents the highest level of concern and is explained as the particular “product will cause serious adverse health consequences or death.”

  • Class II FDA Recall

This suggests that the medical device “may cause temporary or medically reversible adverse health consequences”.

Most of the hernia surgical mesh recalls have been designated with this recall category.

  • Class III FDA Recall

This is when the medical device is not likely to cause adverse health consequences but has a certain level of health notice associated with it.

Are you completely in dark about how to go about the defective hernia repair products? Have you been victim to serious adverse health consequences with the mesh usage? The expert house of herniameshrecall.net will help to get the ideas in place and also let you know if the case is eligible for financial compensation. Visit http://herniameshrecall.net or dial 855-815-0586 to know more.

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