those that have been impacted by a hernia mesh are encouraged to come forward and receive a free legal case review.


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Nearly 90% of all hernia related surgeries will use a hernia mesh. However, it has been found that many hernia meshes are defective and may cause severe side effects for patients. This is largely due to the fact that many mesh manufacturing companies rushed their products to the marketplace without proper testing.

Now, manufacturers are quietly removing their hernia mesh products from the marketplace. Those that have had a hernia mesh implant and have suffered severe side effects including infection and mesh migration are encouraged to come forward and receive a free legal case review.



MAY 2020

2,100+ individual claims have been filed against Atrium Medical Corp® after thousands of patients begin to suffer from serious adverse side effects caused by the mesh.

September 2019

More than 2,000 lawsuits are now pending in the Northern District of Georgia for the Ethicon Physiomesh® after the mesh caused serious injuries.

june 2019

a report that showed 2,478 Bard® hernia mesh cases and 2,167 Ethicon® hernia mesh cases have been filed.

march 2018

from 2005 to 2018., hernia mesh manufacturers have recalled over 211,000 units.

Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Atrium®, Bard Davol®, Covidien®, Ethicon®, or any government agency. is the property of Shield Legal LP. 7180 S Pollock Drive, 2nd Floor, Las Vegas, NV 89119

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