A hernia mesh lawsuit is a claim against the mesh manufacturer by the victim who received the implant and then experience severe health complications and injuries. The lawsuits contend that the mesh devices were imperfectly designed and that the makers failed effectively to advise patients of known and predictable risks and side effects.
There are at present thousands of lawsuits awaiting against multiple manufacturers, most of them as part of a central multi-district litigation (MDL).
The lawsuits seek to recover the financial damages for these victims, including compensation for:
- loss of future earning capacity,
Manufacturers of defective hernia mesh implants have been sued for the following major injuries which have been commonly reported by the victims:
You might be entitled for compensation if you have been affected by the following company's products:
- Atrium Medical Corporation
The product liability lawyers will review potential claims for victims who have suffered painful complications following the repair surgery, which resulted in the need for additional surgery to remove hernia mesh from their body.
- Atrium C-Qur, the production of which meshes have was permanently stopped on February 4, 2015 in compliance with an order from the U.S. Food and Drug Administration (FDA).
- Ethicon Physiomesh, which was willingly recalled after proper investigation which showed a higher-than-normal rate of hernia recurrence, requiring corrective surgery.
- Bard Ventralex ST, a plastic polypropylene hernia mesh product which is known to be associated with serious allergic reactions and side effects.
The lawyers of herniameshrecall.net are ready to pursue financial compensation for those who have suffered the harmful side effects of defective hernia mesh.
For a free, legal and confidential consultation, they can be reached at (855)
815-0586.