hernia mesh procedure

Are hernia meshes necessary for the all patients?

Hernia mesh procedure or hernioplasty is one of the most frequently conducted surgeries in the US today. According to latest reports, more than a million patients undergo this procedure to fix their hernias, a bulge in the abdomen created by the internal organs pushing through the weaker sections of the abdomen. In the method, the surgeon cuts a small slit in the affected region to push the displaced organs back to their position. Following that, they insert a small polypropylene mesh, so that the organs cannot push back through the compromised region.

The surgery involving meshes became quite popular in the past two decades, as the procedure was supposed to prevent the hernia recurrences – a major issue in traditional hernia surgery. However, in the given period multiple patients have come forward with issues after being fitted with the implant.

Complications associated with the polypropylene meshes

The polypropylene meshes are known to cause some amount of discomfort to the patients after surgery. However, in some cases, patients have suffered from the following complications:

  1. Adhesion
  2. Chronic Pain
  3. Infection
  4. Bowel obstruction
  5. Organ perforation
  6. Inflammation and swelling in the area of the incision
  7. Mesh rejection
  8. Mesh migration
  9. Nerve damage

If not treated on time, these issues can lead to life-threatening situations. In most cases, patients require numerous surgeries to fix these issues. Unfortunately, these complications are expensive and risky, which puts an extra dent in the already punctured morale of the victims.

When do these complications crop up?

A complication following hernioplasty or hernia mesh procedure can crop up any time after the surgery. As per a study, the chances of complications can arise within five years after the surgery.

The paper suggested that a substantial number of patients need reparative procedures to fix the complications.

The reason behind these complications

As per experienced lawyers, the designed flaw of some of the hernia meshes is the main reason why these implants fail to deliver the best results. With time, the mesh might shrink or get detached from its anchored points, leading to the severe internal injuries for the victims.

The big corporations launched a product that was not tested thoroughly, jeopardizing the life of the patient. Plus, they assured the doctors that the medical device would help to manage the hernia and provide the patients with lasting relief.

The agencies like Mesh Hernia Lawsuit are coming forward to help the patients with the complications associated with hernia meshes. You too can approach them with your harrowing story after being fitted with these implants. For more information, visit https://meshhernia.com/ or call 855-817-3922.

hernia surgery complications

Complications from defective hernia mesh implant


Hernias occur when the intestines or some other damaged or weakened abdominal part protrudes through the muscle wall. To repair hernias, surgeons for the last decade have used surgical mesh.

hernia surgery complications

Initially, these meshes were considered to be effective; however, questions have emerged about their safety soon after their release in the market.

The U.S. Food and Drug Administration since March 2010 have subjected some surgical mesh products to recall as they have been shown to be associated with some serious life threatening complications.

Some of the most prevalent injuries that have been the concern for the attorneys as hernia surgery complications are:

  • Adhesions – scar tissue forming between bodily tissues that can lead to digestive problems, chronic pain and bowel obstruction
  • Bowel obstruction – a blockage of the small or large intestines can constrict blood flow
  • Intestinal perforation – bowel perforation happens when the mesh erodes through the tissues or punctures it. It causes peritonitis and sepsis
  • Mesh rejection – it happens when the body’s immune system is triggered leading to inflammatory response

Many of the risks of adhesions linked with the surgical mesh were not disclosed to physicians or patients before they were being implanted with it. In the past years, the harmful effects of the hernia mesh came into picture when more and more patients are developing adhesions and complaining about them.

The victims of the defective mesh implant can file for lawsuit and claim for damage award the following:

  • ongoing and the future medical costs
  • loss of wages
  • inability or decreased chance to earn in future
  • cost for the emotional difficulties, pain and suffering
  • cost of emergency hospitalization

The brands that have been recalled:

  • R. Bard
  • Johnson & Johnson
  • Endo International plc
  • Coloplast
  • Boston Scientific

To find out whether your case is entitled for financial compensation, get in touch with the experts of the meshhernia.com team. Find out more about how they can help to achieve the damage awards from the mesh lawsuits, visit https://meshhernia.com/. Dial 855-817-3922 to schedule a free appointment with the experts and get a free evaluation of your case.

New Questions Raised on Implant Recalls

New Questions Raised on Implant Recalls

When implanted medical device products starts breaking, what is the basic human response from the creators of those devices?

One answer can be found in the case of a hernia repair device made by a subsidiary of C. R. Bard Inc. In late 2005, the company sent out a recall, urging doctors to stop using some versions of the product because a plastic component could break and cut through a patient’s internal organs and tissue.

At the time, Bard executives said they knew about some serious injuries potentially caused by the device, which is known as the Kugel patch. Since then, the Food and Drug Administration has received reports of more than 80 injuries and other problems possibly related to it, including several fatalities.

Bard officials said recently in a statement that they had not recalled the product sooner because complaints about failures were too few and unrelated to raise any alarms. The company also said that both it and the subsidiary, Davol Inc., had reacted responsibly.

But when F.D.A. officials inspected Davol in early 2006, they apparently found other reasons that company officials and the agency might not have been alerted earlier. For example, inspectors reported “discrepancies” and “inconsistencies” in how Davol tracked and analyzed device-related complaints.

And, in several instances, Davol also did not accurately report the possible severity of complaints to the agency, a copy of an inspection report obtained by The New York Times under the Freedom of Information Act shows.

You can read the full article here >> full story.

So the FDA Says ‘No More Mesh’ for Hernia Repairs…

So the FDA Says ‘No More Mesh’ for Hernia Repairs…

Which came first, the chicken or the egg? Well, in this case, was it the gynecologic surgeons who were too quick to adopt mesh in the O.R. or the FDA’s 510(k) approval process was too quick to allow mesh in gynecologic surgery. Who is to blame? You can read the full story here!

The problem now is that the mesh in some procedures (but not all) has a tendency to erode — wearing through the vaginal mucosa and exposing its rough and uncomfortable surface to the patient and her sexual partner — or constrict and scar, causing tightening and discomfort.

Some of these procedures have been stunning successes. Procedures that place mesh under the urethra (the tube that carries urine from the bladder to the outside) are generally quick, require minimal recovery, are safe and are proven to cure a particular type of incontinence. (This use of mesh is not part of the FDA warning, although this distinction may be lost on patients.)

But other mesh procedures, in which mesh is used to support one or more of the vaginal walls, have led to complications. The mesh used for these surgeries is essentially the same mesh used (successfully) by general surgeons to repair hernias and other abdominal wall defects.

Medicine cross pollinates from one field to another — we call it innovation. There is a long tradition of taking drugs and devices approved for one purpose and using them for another purpose. Once a device is FDA approved, physicians can (at their peril) use them for pretty much whatever they like. So it is with mesh. I believe that making it harder to get mesh approved for hernia repairs isn’t going to make it less likely to erode into women’s vaginas — it’s just going to slow down the process of getting discoveries into the clinics and into the O.R.

And the cowboy gynecologic surgeons? These are the innovators who brought about the successful mesh sling procedures that now cure 95 percent of women of incontinence in 30 minutes (when surgeries with 50 percent success rates used to take 5 hours in the O.R. and require weeks of recovery). Millions of women have benefited from the extraordinary era of innovation in gynecologic surgery over the past 15 years. Do we really want these surgeons to stop innovating?

Remember to check out the full story here!