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Is My Hernia Mesh Recalled?

If your hernia was repaired with a surgical mesh implant, it is important for you to know whether your hernia mesh was recalled by the U.S. Food and Drug Administration (FDA).

Some of the hernia mesh recalls since 2005 are:

  • Bard and Davol recalled Composix Kugel mesh
  • Ethicon Proceed Surgical Mesh
  • Atrium Medical Corporation C-QuR V-pack Mesh
  • Ethicon Physiomesh Flexible Composite Mesh
  • Atrium Medical Corporation’s ProLite Mesh
  • Sofradim Production Versatex Monofilament Mesh

It is not uncommon for patients not to know the specific mesh manufacturer and brand used in surgery. Contact your surgeon’s office to get that information from your medical records.

Why Hernia Mesh Products Were Recalled By The FDA?

Manufacturers have a responsibility to ensure that the products they put on the market are safe. FDA recalls happen when there is a probable chance that using a defective product will cause serious or even deadly health consequences.

The FDA recalled hernia mesh implants for various reasons, including:

  • Mislabeling of packaging documentation
  • Mesh being made from counterfeit materials
  • Design/manufacturer defects in the products

Before the first hernia mesh recalls were issued, the FDA published several warnings about the potentially harmful and dangerous health effects of surgical mesh implants. Despite the warnings, however, manufacturers continued to produce and market these mesh implants. As a result, more patients have had to experience unnecessary and sometimes severe pain, complications, and revision surgery.

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Common Complications Associated With Recalled Mesh

Many complications related to hernia repair with surgical mesh implants that have been reported to the FDA have been associated with recalled mesh products no longer on the market. FDA analysis found that recalled mesh products were the main cause of bowel perforation and obstruction complications. Some other potentially harmful events that can occur following hernia repair with recalled mesh are when the mesh moves from the original surgical site (mesh migration) and when the implant contracts in the body (mesh shrinkage).

The most common complications associated with recalled mesh are:

  • Chronic and severe pain
  • Infection
  • Recurrence
  • Adhesion to the bowel wall
  • Obstruction of the bowel
  • Perforation of the intestines
  • Mesh migration
  • Mesh shrinkage
  • Higher risk of recurrence
  • Increased chance of requiring revision surgery
  • Fistulae (Abnormal connections between internal organs, intestines, or blood vessels)

If you are suffering from any of these complications, it may indicate a potentially dangerous problem. There is a chance that your body may be rejecting the mesh implant. Contact your surgeon to discuss any issues you may be experiencing.

Common Symptoms Of Hernia Mesh Rejection

After any surgery, it is expected that patients will experience some pain and discomfort. However, if you had hernia repair surgery and are not feeling well, there is a chance your body may be rejecting the mesh implant.

The most common hernia mesh rejection symptoms are:

  • Debilitating abdominal pain
  • Extreme fatigue
  • Irritable bowel syndrome
  • Flu-like symptoms including fever and chills
  • Redness and inflammation near the incision site
  • Nausea
  • Vomiting

Symptoms of hernia mesh rejection do not immediately show up, and can easily be thought of as an indication of a bad cold or flu. Unfortunately, these symptoms develop into health serious complications that can be difficult and expensive to treat. If you are experiencing any of these symptoms, talk to your surgeon as soon as possible to avoid any further complications.

Hernia Mesh Manufacturers Are Liable For Your Injuries

Medical product manufacturers are responsible for the injuries their implants cause patients. Hundreds of thousands of hernia repair patients have reported serious internal injuries. As a result, the number of personal injury and product liability lawsuits filed in state and federal courts is increasing. The lawsuits claim the hernia mesh implants have manufacturing and design defects that directly cause dangerous complications to hernia mesh implant patients hence the hernia mesh recalls.

Damages Hernia Mesh Patients Can Recover

Hernia mesh patients often seek compensation for many types of damages, including:

  • Medical expenses
  • Lost wages
  • Future lost earning potential
  • Pain and suffering
  • Mental anguish
  • Permanent disabilities, impairment, or disfigurement

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