Hernia Mesh Lawsuit
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Hernia Mesh Lawyer Wisconsin - Hernia Mesh Lawsuit Wisconsin
Have you or a loved one suffered side effects after hernia mesh surgery? You may be entitled to financial compensation from the manufacturer. Call us today for a free case review. Call Toll Free 1-866-777-2557 or use our online contact form below and a Lawyer will get back to you within 24 hours to discuss your possible case. Hernia Mesh Lawyer Wisconsin. Time is limited, so please contact us today. Hernia Mesh Lawsuit Wisconsin
We are investigating several hernia mesh systems including some manufactured by Atrium, Bard Davol, Ethicon (a division of Johnson and Johnson) and Covidien.
Hernia Mesh Lawyer Wisconsin
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Hernia Mesh Lawyer Wisconsin
The Food and Drug Administration (FDA) regulates medical devices like hernia mesh. The FDA assures that items under their purview are not only effective, but that they are safe. Products are assessed and monitored while on the market by the FDA and the manufacturers. Input is also received from other governmental agencies; professionals, such as doctors; and the public. When concerns are raised about a product or device, this can lead to a product recall.
Hernia Mesh Lawyer Wisconsin
The recall process is triggered a number of different ways. A manufacturer may discover a problem and will contact the FDA. This can result in a voluntary recall that the company itself initiates. An FDA inspection can unearth defects or safety hazards; another governmental agency, the CDC or state health system, can contact the FDA about problems; and consumers and medical professionals may directly contact the FDA to report hazards. When manufacturers do not voluntarily recall their harmful, defective, or illegal products, the FDA can mandate a recall. Recalls can happen due to the emergence of unexpected health risks, mislabeling, contamination, or manufacturing defects. The recall addresses the safety aspect of the product, but does not indicate intentional bad behavior on the part of the manufacturer.
Hernia Mesh Lawyer WI
Hernia mesh devices are typically Class I devices, deemed to have a reasonable likelihood of serious adverse health consequences or death if functioning improperly. Some mesh devices have been subject to a number of recalls throughout the 2000s by FDA mandate and through voluntary manufacture recall. Over the years 2005-2007 Bard Davol recalled thousands of units of their Kugel Hernia Mesh because of the risk of a memory recoil ring present in the patches to break. When the ring would break, it could lead to bowel perforations or chronic intestinal fistulas. Atrium Medical recalled nearly 150,000 units of its C-QUR Mesh for improper packaging in 2013. The FDA warned Atrium about lack of proper testing that was potentially leading to increased incidences of infections. Despite the recall, very little mesh was actually recalled; doctors simply received notice from Atrium of problems with the mesh’s coating.
Hernia Mesh Lawsuit Wisconsin
Ethicon has also recalled a number of its Proceed Mesh units in 2005, 2010 and 2014 because of a problem with the loss of laminate coating on the mesh that would allow the mesh to come in direct contact with organs and increase the chance of adhesions and fistulas. Currently, there are consumer lawsuits against all three of these manufacturers for the complications suffered that has been attributed to faulty mesh. The lawsuits claim that the mesh was designed poorly and that the mesh manufacturers knowingly hid the dangers patients would face.
Hernia Mesh Lawyer Wisconsin