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Read up on the latest concerning hernia mesh lawsuits. Our law firm litigates hernia mesh lawsuits. We handle most cases in-house and firms refer their hernia mesh cases to us. This page is where we’ll provide hernia mesh updates concerning hernia mesh lawsuits.

Before diving in, we want to clarify one thing. Some folks think there may be a hernia mesh class action lawsuit. We are not aware of any hernia mesh class action lawsuit. A class action lawsuit involves an individual or small number of individuals filing a lawsuit on behalf of similarly situated people, litigating, and resolving the class action for them and then those other people – who do not have their own lawsuit – being notified to opt in or out of the class action settlement. Here, the hernia mesh lawsuits are individual cases, not a class action. 

KBA Continues Litigating Hernia Mesh Lawsuits

Some injured patients sued various hernia mesh companies across the country. Atrium, Bard, Covidien, Ethicon, and Lifecell are some examples of recent hernia mesh litigations. The hernia mesh lawsuits involve cases where a patient had a hernia mesh removal. Some law firms have stopped representing patients; KBA has not. KBA Attorneys litigates Atrium, Bard, Covidien, and Lifecell (Strattice) cases.

We work up our hernia mesh cases personally. Our hernia mesh attorneys file lawsuits, take depositions, and try hernia mesh lawsuits. We work with preeminent experts – scientists and doctors. Our hernia mesh lawyers litigate hernia mesh lawsuits assertively. We publish hernia mesh updates here.

Thousands of Hernia Mesh Failures for Decades

Hernia mesh failures occur. Surgeons place hernia mesh in patients to repair hernias. In some, there is then a hernia mesh removal. For decades we have seen vast hernia mesh failures. These hernia mesh failures lead to hernia mesh lawsuits.

As of 2024, thousands of lawsuits exist across the country. These lawsuits are against manufacturers such as C.R. Bard, LifeCell (Strattice), Covidien, and Atrium Medical Corp. The KBA team is led by Partner Robert Price and Attorney Keith Smith

The claims from patients are complaints that the hernia mesh used for their hernia surgeries have caused health issues such as chronic pain, infection, adhesions, hernia recurrence, bowel perforation, bowel obstruction, mesh migration, mesh rejection, and more. Some patients had to have the mesh removed or undergo hernia revision surgery.

If you have experienced any of these symptoms due to hernia revision surgery, then contact KBA Attorneys for professional legal assistance. In the meanwhile, here’s the latest in hernia mesh lawsuits. Check back for hernia mesh updates. 

Who Are Plaintiffs Suing in Hernia Mesh Lawsuits?

     Allergan/LifeCell

Our firm stated these hernia mesh lawsuits. We studied the science, developed the experts, assembled a team, and filed the first hernia mesh lawsuit against this defendant.

LifeCell made a mesh from pig tissue called Strattice. Thus, it’s a biologic mesh. It also made a product from dead humans called Alloderm. There was litigation about that product years ago, which resolved. A NJ state court consolidated cases around 2014. Defendants successful eliminated some of the plaintiffs’ claims.

KBA Attorneys filed lawsuits with their co-counsel, Cohen and Malad (“CM”), against LifeCell concerning the Strattice mesh. This litigation is consolidated in NJ state and federal court. Plaintiffs recently survived Defendants’ challenges to various claims. LifeCell Must Face Trial in N.J. Bellwether Strattice Hernia Mesh Case, Judge Rules | HarrisMartin Publishing. KBA is proud of attorneys Robert Price and Keith Smith, along with attorneys at CM, for this victory. The defendant won the first trial, but these hernia mesh lawsuits will continue.

The first trial went Defendants’ way in state court in New Jersey. We are appealing some rulings. Another trial will take place in the spring of 2025. It also involves hernia mesh removal. Our mesh hernia lawyers are ready to fight the hundreds of hernia mesh lawsuits that remain. 

Current status: April 2025, defense pick trial starts.

     C.R. Bard Hernia Mesh

Bard has the largest hernia mesh market share. This hernia mesh manufacturer created the 3DMax hernia mesh. The 3DMax was put on the market in 2009 and is made up of a material called polypropylene. The 3DMax did not have to go through pre-market studies and was approved in October 2008 through the 510(k) program.

Bard claims that the 3DMax Mesh is fixation-free, easy to position, and reduces pain for patients. However, the polypropylene material has been known to cause many health complications such as chronic pain, mesh migration, and mesh rejection. Some patients even require additional surgery.

C.R. Bard’s Composix Kugel Mesh was another defective medical device manufactured by the company that was recalled. This particular product was recalled in 2005, 2006, and 2007. There have been a plethora of lawsuits involving Kugel Mesh. Other hernia mesh products that have been repeatedly recalled include:

  • Bard Composix E/X
  • Bard PerFix Plug
  • Bard Sepramesh
  • Bard Ventralex ST

Many Bard Lawsuits are being filed with allegations of the company selling defective hernia mesh. These lawsuits are in state and federal courts all over the country. If you have experienced complications because of a C.R. Bard hernia mesh medical device, then contact a professional attorney today.

          Bard hernia mesh products KBA Attorneys are litigating:

  • Bard Mesh (Flat Sheet; Flat Sheet w/Keyhole)
  • Composix
  • Composix E/X 
  • Composix L/P 
  • Composite Prosthesis/Composix 
  • Composix Kugel (only if the product was removed within the last three years unless the product reference/cat numbers are 0010201, 0010203, and 0010205)
  • Kugel
  • Marlex  
  • Perfix Plug 
  • Perfix Light Plug 
  • SepraMesh – if manufactured after 12/14/2007 by Bard
  • SpermaTex 
  • Ventralex 
  • Ventralex ST 
  • Ventralight ST 
  • Ventrio 
  • Ventrio ST  
  • Visilex 
  • 3DMax 

The vast majority Bard hernia mesh lawsuits are effectively on hold. There is an action in federal court and in Rhode Island state court. Our firm litigates Bard hernia mesh lawsuits in both venues.

Covidien Hernia Mesh

Medtronic now owns Coviden. Based in MA, Covidien created a line of hernia mesh years ago. They had a fairly large market share.

There are two broad Covidien hernia mesh categories, monofilament (“mono”) and multifilament (“multi”). There are Covidien hernia mesh lawsuits in a few places including state court in MA, a federal MDL, and Minnesota, we believe. KBA Attorneys are active in the MA venue where we have filed well over a thousand cases.

          Covidien hernia mesh products KBA is pursuing:

  • Progrip (mono)
  • Parietex (multi)
  • Parietex Composite (PCO) (multi)
  • Parietex Composite Open Skirt (PCO OS) (multi)
  • Parietex Composite Parastomal (PCO PM) (mono)
  • Parietex Composite Hiatal Mesh (PCO 2H)
  • Parietex Composite Ventral Patch (PCO VP) (mono)
  • Parietex Flat Sheet Mesh
  • Parietex Folding Mesh
  • Parietex Hydrophilic Anatomical Mesh (multi)
  • Parietex Lightweight Monofilament Mesh (mono)
  • Parietex Optimized Composite Mesh (multi)
  • Parietex Optimized Open Skirt Mesh (multi)
  • Parietex Progrip (mono)
  • Parietex Plug and Patch (mono)
  • Symbotex (mono)
  • Surgipro – all types (mono and multi versions)

Our firm litigates Covidien hernia mesh lawsuits. We are pursuing both groups of Covidien hernia mesh, monofilament and multifilament. We expect to be even more active in the hernia mesh lawsuits in the coming months.

These hernia mesh updates concerning the active hernia mesh lawsuits are not a hernia mesh class action lawsuit. We are not aware of a hernia mesh class action lawsuit. The hernia mesh lawsuits are individual cases mostly consolidated before a federal or state court judge.

What Are Some Hernia Mesh Failure Symptoms?

The FDA has listed common side effects of hernia surgery complications. Here’s what FDA says on one of it’s hernia mesh pages:

Based on the FDA’s analysis of medical device adverse event reports and of peer-reviewed, scientific literature, the most common adverse events for all surgical repair of hernias—with or without mesh—are pain, infection, hernia recurrence, scar-like tissue that sticks tissues together (adhesion), blockage of the large or small intestine (obstruction), bleeding, abnormal connection between organs, vessels, or intestines (fistula), fluid build-up at the surgical site (seroma), and a hole in neighboring tissues or organs (perforation). For hernia repair with mesh, additional adverse events include migration or shrinkage (contraction) of the mesh itself, which may more likely be associated with the previously mentioned complications of hernia repair.

In our experience, we have seen several symptoms of hernia mesh failures. Some of them follow:

1. Chronic Pain

  • Persistent or worsening pain at or near the surgical site.
  • Pain that interferes with daily activities or requires ongoing medical treatment.

2. Infection

  • Redness, swelling, or warmth around the surgical site.
  • Fever, chills, or other systemic signs of infection.
  • Abscesses or draining wounds indicating an infected mesh.

3. Mesh Migration

  • Movement of the mesh from its original position, leading to organ damage or bowel obstruction.
  • Symptoms include severe abdominal pain, bloating, or changes in bowel habits.

4. Mesh Erosion

  • The mesh eroding into nearby tissues or organs, causing internal damage.
  • Symptoms may include bleeding, organ dysfunction, or abnormal discharge.

5. Bowel Obstruction

  • Partial or complete blockage of the intestines.
  • Symptoms include nausea, vomiting, constipation, and severe abdominal pain.

6. Recurrence of the Hernia

  • The hernia returning despite the mesh repair.
  • May indicate product failure or improper surgical technique.

7. Adhesions

  • Scar-like tissue forming around the mesh, causing organs or tissues to stick together.
  • Symptoms may include chronic pain and restricted movement.

8. Seromas

  • Fluid buildup around the surgical site, leading to swelling and discomfort.
  • May require drainage or additional treatment.

9. Perforation

  • The mesh puncturing nearby organs, leading to severe complications.
  • Symptoms include acute pain, infection, or organ dysfunction.

10. Allergic Reaction or Rejection

  • The body rejecting the mesh material, resulting in inflammation or systemic symptoms like rash or fatigue.

11. Neurological Issues

  • Nerve damage caused by the mesh or its placement.
  • Symptoms include numbness, tingling, or sharp shooting pains.

The most common result of hernia mesh product failures that we have seen is hernia mesh removal surgery after  recurrent pain. We file hernia mesh lawsuits where a patient had the hernia mesh removed.

What to Do After Hernia Mesh Removal

Step 1: Focus on Your Recovery

  • Rest and heal: Avoid strenuous activities, especially heavy lifting, during recovery.
  • Monitor for infection: Watch for redness, swelling, or discharge at the incision site.
  • Attend follow-ups: Ensure your hernia repair is stable and monitor for new complications.
  • Manage pain carefully: Discuss options with your doctor to avoid long-term issues or addiction risks.

Post Hernia Mesh Removal Step 2: Review Your Medical Records

  • Gather:
  • Surgical reports (implantation and removal details).
  • Doctor’s notes (complications, infections, allergic reactions).
  • Medical tests and imaging (CT scans, X-rays, or MRIs).

Step 3: Understand Your Complications

  • Infection: Bacterial contamination (e.g., meshoma).
  • Chronic pain: Persistent pain due to nerve or organ adhesion.
  • Mesh migration or erosion: Can lead to organ damage or bowel obstruction.
  • Hernia recurrence: May require additional surgeries.

Post Hernia Mesh Removal Step 4: Seek Legal Assistance

  • Eligibility for compensation: For defective mesh or complications caused by products from Bard, Covidien, Atrium, Ethicon, or Lifecell.
  • How KBA Attorneys can help:
  • Free consultations.
  • Comprehensive case review with top medical experts.
  • Expertise in hernia mesh litigation, from pre-trial to courtroom representation.
  • Maximize compensation for medical bills, pain, and lost wages.

Step 5: Act Now

  • File your claim promptly: Statutes of limitations may apply.
  • Secure your rights: Delay could reduce your chances of compensation.

To learn more, visit our blog for detailed insights about hernia mesh removal and legal options.

Patients who have had Transvaginal Mesh (TVM) removal should follow the same procedure essentially. These steps are essential to staying healthy and prepared for anything that may follow removal of the mesh.

Contact a Defective Hernia Mesh lawyer

Do not let these hernia mesh manufacturers escape justice. They are responsible for thousands of injuries, some of which are severe and life-threatening. Each hernia mesh case is different and should be treated separately, however past hernia mesh injury lawsuits have led to hundreds of thousands of dollars and more. One verdict was seven figures. Again, each case is different and past results do not guarantee future results.

Contact a hernia mesh attorney at HerniaMesh@KBAattorneys.com if you or a loved one have experienced any of the below symptoms as a result of a defective hernia mesh product:

  • Infection
  • Bowel Obstruction or Perforation
  • Adhesion (Scar-Like Tissue That Sticks Tissues Together)
  • Bowel Obstruction (Blockage Of The Large Or Small Intestines)
  • Bowel Perforation (A Hole Near Organs Or Tissues)
  • Hernia Mesh Rejection
  • Hernia Mesh Migration
  • Hernia Recurrence
  • Fistula Formation (Abnormal Connection Between Intestines, Vessels, Or Organs)
  • Seroma (Fluid Build-Up Near The Surgical Area)
  • Inflammatory Disease
  • Mesh Erosion

Our team works to protect the people from medical device companies like C.R. Bard, Covidien, LifeCell, and Atrium Medical Corp. Contact KBA Attorneys to learn how you could get compensation for your hernia mesh

What are the Allegations?

Plaintiffs allege that these companies – C.R. Bard, Covidien, LifeCell, and Atrium Medical Corp. – have an obligation to design medical devices that are safe for patients. There are thousands of innocent people who have already used their defective product for their hernia surgery and have suffered severe health complications. The hernia mesh lawsuits claim that manufacturers such as Bard, Covidien, LifeCell, and Atrium have:

  • Failed to Warn Patients and Doctors of the Harmful Side Effects Linked to Their Defective Medical Device; for example, the Risks were greater than disclosed.
  • Sold A Medical Device That Did Not Perform as Was Intended by The Companies or Expected by the Consumers.
  • Sold A Medical Device That Was the Direct Reason for Revision Surgery.
  • Designed A Defective and Unsafe Medical Device.

Are You Eligible for a Hernia Mesh Lawsuit?

Our initial intake criteria is below, but we encourage you to call us if you are not sure whether your case fits in the criteria.
  • You were over 18 years old when the doctor implanted hernia mesh inside you; 
  • You were not pregnant at the time of implant when the surgeon implanted the hernia mesh inside you
  • A doctor put (implanted) hernia mesh inside your body on or after May 1, 2014
  • If it happened BEFORE May 1, 2024, we will consider your case if you have medical records showing what hernia mesh product the surgeon implanted into you AND showing a surgery to remove or revise/modify that same hernia mesh;
  • A doctor removed or revised (modified) the mesh due to a problem with the mesh

If this is your experience, KBA Attorneys may be able to help. Patients who discover that the hernia mesh used in his or her surgery was recalled should first speak with a medical professional for medical assistance. The next step should be to contact an experienced attorney so they may review your case and give you information about receiving monetary compensation. You can reach the Hernia Mesh team directly at HerniaMesh@KBAattorneys.com, you can also contact us here.

What is the average payout for hernia mesh lawsuit?

No one can really say. First, what does average payout for hernia mesh lawsuit mean? If it means just a jury verdict, we do have some data. If it includes settlements, that’s impossible to say  because most are confidential at this point.
What is the average payout for hernia mesh lawsuits? Let’s look first at jury trial verdicts. There have been several jury trials. At least two defense verdicts, which as zeros, bring the average down. There was a $250,000 or so verdict years ago. That same court, the Bard MDL court in Ohio, saw a subsequent $500,000 verdict. A state court jury awarded a Bard client $4,800,000. So, what is the average payout for hernia mesh lawsuit? $1,110,000. A better question may be What is the average settlement for hernia mesh lawsuit? That is more tricky. 
As the leading hernia mesh attorneys, we share our knowledge. Here is some additional information about hernia mesh from our blog: