If you have used a Hernia Mesh and suffered complications or serious side effects, you owe it to yourself and your family to contact us for a free evaluation to determine if you are due damages for your injuries.
The hernia mesh lawsuits claim that the manufacturers designed defective products and failed to adequately warn the medical practitioners of the severe side effects and complications associated with using these devices.
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Thousands of victims have already filed lawsuits citing device failure and adverse complications they were not aware of.
read moreGoing against medical device giants is not only intimidating but also scary. Contact us now for a free consultation!
What we do is fight for your rights to get you the largest possible settlement to compensate you for your injuries or death. We know medical and hospital expenses are out of this world, and when you are injured through no fault of your own, we go after those responsible for your injuries and see that you're treated fairly, and with the respect and caring that you deserve.
A hernia mesh is described as a small, simple medical device used to fix or repair hernias, which occur when tissues or intestines protrude through the weak areas of flesh.
According to the plaintiff attorneys, some of the hernia mesh products were defectively designed and had been causing unnecessary injuries that would not have occurred in the first place if the manufacturers properly warned the medical providers.
The hernia mesh lawsuits have been trekking in steadily since the mid-2010s. The US Food and Drugs Administration had to recall a number of the hernia mesh products following reports form the patients who had suffered adverse complications.
Among the prevalent manufacturers of the hernia mesh products include Atrium, Bard Inc., and Ethicon. While there are many manufacturers with products in the market, these three are the makers of the products that have entirely been subject to many lawsuits in the past years.
The hernia mesh lawsuits claim that the manufacturers designed defective products and failed to adequately warn the medical practitioners of the severe side effects and complications associated with using these devices.
Severe hernia mesh complications can occur when a defectively designed product is used, or the doctor makes a mistake during the implanting. Some of the hernia mesh manufacturers are accused of knowing the problem these devices can cause but failed to warn the patients and medical providers.
If you're having some doubts, get a copy of your medical records from the past implant surgery. You can seek a law firm's help to obtain this documentation or simply contact the surgeon in charge of your implant.