Hernia Mesh Lawsuit
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Hernia Mesh Lawyer San Diego CA - Hernia Mesh Lawsuit California
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 consultation. Toll Free 1-866-777-2557 or use our online contact form below and a San Diego CA Hernia Mesh Lawyer will get back to you within 24 hours to answer your questions. Time is limited, so please contact us today. Hernia Mesh Lawsuit California
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 San Diego California
Most people realize that the FDA is involved in the regulation of medical products. When devices slide below basic safety and effectiveness expectations, it is their duty to notify individuals and issue recalls. What most people don’t realize is that it is critical to check with the FDA website for the most updated information concerning medical device recalls and safety concerns.
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Medical device manufacturers typically issue product recalls before they are requested to do so by the FDA, or sometimes in conjunction with the FDA and its investigators. Yet another way the FDA notifies consumers about safety issues relating to medical devices are though what are called safety communications. This is the case when it comes to hernia mesh. Surgical mesh is commonly used to support fragile or impaired tissue and is generally made out of synthetic substance. Any time fatty or other tissues protrude from the abdominal walls, it usually becomes necessary to make use of surgical mesh to bolster the area impacted by the hernia.
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Utilization of mesh can certainly reduce recurrence of the problem, but can result in problems associated to the mesh. In a Safety Communication from 2014, the FDA reported that it had obtained a selection of studies concerning mesh-related complications. Some of the issues reported to the FDA include things like nerve and blood vessel injuries, intestinal adhesions, and infection. While they reported that a majority of the incidents related to products that had already been recalled, they are needing to continue to examine the situation and have asked for consumers and doctors to continue to study any concerns they may have due to mesh products.
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Producers have pulled and recalled systems by themselves due to a range of factors. Atrium Medical and Ethicon have recalled mesh for packaging issues, but Bard Davol and Ethicon have also recalled products for safety concerns. 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. People are encouraged to submit issues with products regulated by the FDA. Reporting issues as soon as possible can make certain that quick consideration is given the product in question.
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When reporting, be prepared with all of the crucial reporting info such as names and contact information for the affected folks, contact info for any medical companies who supplied medical help if applicable, product codes or identifying marks on the content label or container, names and addresses of store where the product was acquired and of the manufacturer. Reports can be submitted online via the MedWatch system or by getting in touch with the local FDA Complaint Director.