Hernia Mesh Lawsuit
Hernia Mesh Lawyers
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Hernia Mesh Lawyer Colorado - Hernia Mesh Lawsuit Colorado
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 Colorado. Time is limited, so please contact us today. Hernia Mesh Lawsuit Colorado
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 Colorado serving entire state including:
- Grand Junction
- Denver
- Arvada
- Broomfield
- Parker Town
- Fountain
- Boulder
- Littleton
- Westminster
- Pueblo
- Brighton
- Loveland
- Commerce City
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- Wheat Ridge
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- Colorado Springs
Hernia Mesh Lawyer Colorado
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.
Hernia Mesh Lawyer Colorado
This is the case with respect to hernia mesh. 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.
Hernia Mesh Lawyer Colorado
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. Manufacturers have withdrawn and recalled devices themselves due to a variety of reasons. Atrium Medical and Ethicon have recalled mesh for packaging issues, but Bard Davol and Ethicon have also recalled products for safety concerns.
Hernia Mesh Lawyer CO
Ethicon announced an Urgent Field Safety Notice for some of its hernia kits and composite mesh, citing higher than normal recurrence and revision surgery rates.
Consumers are encouraged to report problems with products regulated by the FDA. Reporting problems as soon as possible can ensure that prompt attention is given the product in question. When reporting, be prepared with all of the necessary reporting information including names and contact information for the affected persons, contact information for any medical providers who provided medical assistance if applicable, product codes or identifying marks on the label or container, names and addresses of store where the product was purchased and of the manufacturer. Reports can be submitted online through the MedWatch system or by contacting the local FDA Complaint Coordinator.
Hernia Mesh Lawsuit Colorado