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Hernia Mesh Lawsuit Lawyers
CohenMalad, LLP attorneys are investigating the cases of patients who were harmed by the hernia mesh. There are now hundreds of Medical Device Reports received by the FDA in relation to hernia mesh that include infections, serious side effects and complications, and even death.
If you or someone you care about has suffered as a result of hernia mesh, contact us today.
Use of hernia mesh began in 2008 following FDA approval through the 510k process. A controversial method for approval, the 510k process enables a new medical device to gain FDA approval by establishing a set of similarities to a current medical device that is already on the market. The lack of rigorous safety and efficacy testing can allow product vulnerabilities to go undetected until patients are affected and begin to suffer.
Hundreds of patients now report having experienced painful, debilitating complications after the surgical mesh was implanted. These serious and life threatening complications include:
- abdominal swelling
- abscess
- fever
- gastrointestinal distress
- infection
- internal bleeding
- migration/relocation of mesh away from the implantation site
- nerve damage
- obstructions
- organ punctures
- painful intercourse
- rejection of the device
- severe pain
- death
If you or someone you care about has suffered as a result of hernia mesh, we can help.
CohenMalad, LLP has 55+ years of experience fighting for the rights of American consumers. Our attorneys are skilled at getting compensation and justice for those who have been injured from using dangerous and improperly regulated or marketed medical devices.
Contact us today so that a knowledgeable medical device liability lawyer from CohenMalad, LLP can provide you with a free case evaluation and discuss your legal options.
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