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Hernia Mesh Lawyer South Carolina - Hernia Mesh Lawsuit South Carolina
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 South Carolina. Time is limited, so please contact us today. Hernia Mesh Lawsuit South Carolina
We are investigating several hernia mesh systems including some manufactured by Atrium, Bard Davol, Ethicon (a division of Johnson and Johnson) and Covidien.
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- Goose Creek
- Aiken
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Hernia Mesh Lawyer South Carolina
The FDA is charged with the regulation of medical devices. When devices fall below safety and effectiveness standards, it is their responsibility to inform consumers and issue recalls. It is important to consult the FDA website, www.fda.gov for the most up to date information concerning medical device recalls and safety concerns. Manufacturers often issue recalls before they are required to do so by the FDA, or in conjunction with the FDA and its investigators. Another way the FDA informs consumers about safety issues surrounding medical devices are though safety communications. This is the case with respect to hernia mesh.
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Surgical mesh is used to support weak or damaged tissue and is typically made from synthetic material. When fatty or other tissues protrude from the abdominal walls, it often becomes necessary to use surgical mesh to reinforce the area impacted by the hernia. Use of mesh can prevent recurrence of the problem, but could result in complications related to the mesh. Consumers play an important role in the FDA’s regulation of medical devices like hernia mesh. Reporting problems can help the FDA identify serious problems with medical devices and prevent even more consumers from suffering complications.
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When a consumer suspects that hernia mesh has caused them a problem, it is possible to submit a voluntary report to MedWatch, the FDA’s Safety and Adverse Event Reporting program. Doctors and other medical personnel must follow particular reporting requirements and manufacturers need to comply with the Medical Device Reporting regulations. The more detail that is provided, the more useful the report is to the FDA. Provide as much of the following information about the hernia mesh as you can: manufacturer name, brand name, catalog number, lot number, size, date of implant, date of removal (if done). You should also include information about the hernia surgery. Include information related to diagnosis (pre- and post-operative), as well as the surgical procedure and method. Describe the hernia (size, location, type) and how the mesh was placed and the fixation method. Finally, provide a detailed description of the complication caused by the mesh. Include the timing, factors and severity.
Hernia Mesh Lawsuit South Carolina
Include if the problem was resolved and if so how. In a Safety Communication from 2014, the FDA reports that it had received a number of reports about mesh-related complications. Some of the complications reported to the FDA include organ injuries, nerve and blood vessel injuries, intestinal adhesions, infection, pain, and recurrence of hernia. While they reported that most of the incidents related to products that had already been recalled, they are eager to continue to evaluate the situation and have asked for consumers and doctors to continue to report any issues they may have with mesh products.
Hernia Mesh Lawyer South Carolina
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