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Hernia Mesh Lawsuit

Hernia Mesh Lawyers

Hernia Mesh Lawyer San Francisco 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 Francisco 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 Francisco CA


The FDA is responsible for the regulation of medical systems. Whenever devices slide under basic safety and effectiveness expectations, it is their duty to notify individuals and issue recalls. It is crucial to refer to the FDA website, www.fda.gov for the most recent information regarding medical device recalls and safety considerations. Producers generally issue recalls before they are requested to do so by the FDA, or in conjunction with the FDA and its investigators.


Hernia Mesh Lawyer San Francisco California


A different way the FDA notifies consumers about safety issues relating to medical devices are though safety communications. This is the case with respect to hernia mesh. Surgical mesh is utilized to support weakened or damaged tissue and is typically constructed from synthetic substance. Whenever fatty or other tissues thrust outward from the abdominal walls, it generally becomes vital to use surgical mesh to strengthen the area affected by the hernia. Utilization of mesh can certainly reduce recurrence of the problem, but might result in issues connected to the mesh. In a Safety Communication from 2014, the FDA reports that it had received a selection of records regarding mesh-related issues.


Hernia Mesh Lawyer San Francisco California


A number of the problems 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 associated with products that had already been recalled, they are needing to continue to evaluate the situation and have asked for consumers and doctors to carry on to report any concerns they could have because of mesh products. Manufacturers have removed and recalled products on their own due to a variety of reasons. Reporting difficulties as soon as possible can be sure that quick consideration is given the product in question.


Hernia Mesh Lawyer San Francisco CA


When reporting, be ready with all of the critical reporting details which includes names and contact information for the affected individuals, contact details for any medical companies who provided medical guidance if pertinent, product codes or identifying marks on the content label or package, names and addresses of shop where the product was acquired and of the manufacturer.