A hernia mesh lawsuit can help individuals who may have experienced problems that have caused the need for revision of surgical procedure as a result of:
- Extreme Abdominal Pain
- Organ Perforation or Deterioration
- Allergic Reactions
Surgery for Hernia Mesh
The process to file a claim or lawsuit can sometimes be challenging. However understanding the claim process and various hernia mesh recall scenarios can help in knowing what to do next.
Different types of hernias
- Abdominal or central: Occurs in the stomach wall.
- Incisional: Happens at an incision place of earlier surgical procedures or injuries and is the 2nd most common hernia.
- Inguinal: Develops in the genitals and is easily the most recurrent hernia.
- Umbilical: Happens in or across the navel, typically inside the tummy
- Hiatal: Happens in the abdomen basically to an upper part of the stomach.
- Femoral: Takes place at the upper thigh, outside groin or labia and is common in ladies.
There are many different surgical procedures to treat hernia mesh. The procedure appears to be relatively straightforward, but something was wrong with the Kugel mesh hernia patch. Kugel mesh hernia patch challenges did not become well known until 2001 when incidents started being reported.
Some of the people noted side effects such as intestinal obstructions in which the memory coil ring was damaged and resulted in the development of a fistula. There were other complications as well, such as the patch was folded or curled.
These patches were recalled in 2005, and medical professionals had been inquired never to use this particular lot. However, the main reason was that of the high-risk that area of the plastic part of the patch could split off and cut the patient’s organs or tissue with the chance of death.
Hernia Mesh Recall Lawsuit
People who received hernia mesh to fix all kinds of hernias that did not work as intended have sued the companies that produce the hernia. Some examples of recalled mesh include Atrium C-QUR Hernia Mesh and Ethicon Physiomesh Flexible Composite Mesh. Complications that resulted from using the mesh included infections, organ harm, autoimmune issues, adhesions (scar tissue tissues) as well as intestinal obstructions that need additional surgical treatment to fix.
Several types of medical hernia mesh get tested from time to time without having undergone rigorous clinical trials, pre-consumer research or studies. The USA Food and Drug Administration has rules that allow mesh makers to utilize the 510(k) clearance program to have their items tested and used. There have been instances where the mesh has been recalled or production halted due to safety concerns.
The high profile Johnson and Johnson case is one example of a high level genital mesh lawsuit.In January 2016 Johnson and Johnson agreed to settle & pay $120 million for over 2,000-3,000 mesh lawsuits. The payout was significant and marked the first time a large mesh manufacturer agreed to settle a large number of mesh lawsuits. A regulatory filing at that time demonstrated that J&J has had more than 42,000 mesh lawsuits.
This is just one of many lawsuits. In some cases, vendors have had to pay large amounts of money and dealt with many complaints. Hernia mesh can have many defects that can result in very high risk of unreasonable and hazardous injuries and unwanted effects with long term health problems.
Ethicon Physiomesh and Hernia Mesh Lawsuit Settlement
Currently there are some lawsuit claims being contested in federal courts for Ethicon Physiomesh. Though the company Ethicon rejected the urge to recall faulty mesh units in the USA, it did eventually withdraw the Ethicon Physiomesh Flexible Composite Mesh from the market in May 2016.
If you feel you have a valid claim for a hernia lawsuit, you may want to arm yourself with information on some of the following things: (remember the day of the surgical procedure and a few other essential surgical treatment details listed).
- What was the date & time of your surgery?
- What was the brand of mesh?
- Type of your mesh?
- Problems you’ve encountered?
- Did your memory ring crack?
- Was the memory ring and repair eliminated?
- When was it removed?
Cracked memory recoil ring and the hernia patch have led to some significant effects, which include intestinal perforation, bowel blockage, death, as well as severe infections. Blood clotting and severe cardiac arrest are sometimes experienced after the surgical procedure to correct fistulae caused by the damaged memory recoil rings.
Hopefully this information will help you to make a decision and understand the process of a hernia mesh lawsuit.
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