Do you suffer from Hernia mesh complications? Did you receive a mail about a class action on the settlement to resolve claims about the pain and suffering experienced as a result faulty hernia mesh? This review will help you partake in the class action settlement after confirming the authenticity of the mail.
What Is Hernia mesh complications Class Action Settlement?
Hernia mesh lawsuits allege that the mesh devices are defective and that hernia mesh makers failed to warn patients about potential adverse side effects. Some of the medical device makers that have faced lawsuits include Atrium, Bard Davol, and Ethicon.
Hernia mesh injuries alleged in lawsuits include:
- Adhesions (bands of scar tissue)
- Bowel obstruction
- Infection
- Mesh failure
- Meshoma (when mesh has shrunk and can trap nerves/cause chronic pain)
- Migration, etc.
Such complications may require additional hernia surgery to resolve. If you or someone you love has suffered from these or other hernia mesh injuries, you may be able to file a lawsuit and pursue compensation.
What Is This Class Action All About?
Hernias occur when there is a weakness or hole in a muscle or connective tissue, allowing organs, intestines, or tissue to squeeze through the openings and become trapped. This usually results in a bulge that may be visible externally. Hernias can be caused by weakened muscles that have either been present since birth, or are linked with factors like age and repeated strains on the abdominal and groin areas, such as through physical exertion, obesity, pregnancy and frequent coughing. In some cases, hernias are repaired by sewing the muscle walls around the hole directly together. In other cases, a hernia mesh is used to repair the hole.
Hernia mesh is a medical device made of plastic or metal mesh that is placed in the hernia. It strengthens the weakened area and prevents internal organs and tissues from protruding through the hernia causing pain or medical complication.
This high rate of hernia mesh failure led Ethicon to remove the product from the market. In a May 2016 announcement, the removal of Ethicon’s Physiomesh Flexible Composite mesh was categorized as a “Market Withdrawal” and not a recall on the product itself.
Ethicon allegedly failed to clearly define the factors behind the high hernia mesh failure rate. Ethicon said that the failure rate could be due to several factors: design, the physician’s instructions, and patient selection.
If you underwent hernia surgery and suffered side effects, your complications may be the result of a defective mesh product made by one of the four main hernia mesh manufacturers: Ethicon, C.R. Bard, Covidien and Atrium.
Each of these manufacturers has multiple models of hernia mesh products. The following list includes some of the hernia mesh products from each manufacturer:
- C.R. Bard Hernia Mesh Products: Sepramesh, Ventralight ST, Ventralex ST, Ventrio ST, Ventralex, Composix, Kugel, Ventrio, Dulex, Marlex/Sheet Mesh, Perfix, Perfix Lite, 3D Max, 3D Max Lite, and Keyhole Mesh.
- Covidien Hernia Mesh Products: Paretex (including Composite, Plug-and-Patch, Pro-Grip, etc.), Surgipro, and Symbotex.
Who Is Eligible?
The settlement benefits all class members who suffered complications after a hernia mesh device was used to repair a hernia.
How To Be Part of This Settlement
For a class member to partake in this settlement, they must submit their Valid claim on the settlement website.
What Is The Pay For This Settlement?
The pay for this settlement varies and the proof of purchase is not necessary.
Conclusion
As you submit your claim to the settlement website, just like Camp Lejeune class action settlement we have reviewed , you’re doing so under penalty of perjury. You are also harming other eligible Class Members by submitting a fraudulent claim.
