If you or a loved one experienced complications after hernia mesh surgery, you may be eligible to file a hernia mesh lawsuit and pursue compensation. At Salenger, Sack, Kimmel & Bavaro, LLP, our attorneys are currently reviewing claims related to defective mesh products made by manufacturers including Covidien, Bard, Ethicon, Atrium, and more.
Our firm is accepting clients who suffered complications such as mesh migration, chronic pain, infection, or the need for revision surgery after a hernia repair procedure. Contact us today to learn if you qualify.
Hernia mesh devices are used to reinforce weakened tissue during hernia repair surgeries. While many work as intended, thousands of patients have reported painful complications caused by defective mesh products. Lawsuits allege that manufacturers failed to properly test or warn about the risks of their products, including:
Covidien Parietex Surgical Mesh
Covidien ProGrip Composite Mesh
C.R. Bard Ventralex & Kugel Patch
Ethicon Physiomesh
Atrium C-Qur Mesh
As of 2025, over 38,000 hernia mesh lawsuits have been settled, with Bard’s parent company BD agreeing to pay more than $1 billion in October 2024.
Hernia mesh implants can fail, causing serious medical issues. Common complications include:
Chronic pain and inflammation
Bowel obstruction or perforation
Mesh migration to other organs
Fistulas and adhesions
Seromas (fluid buildup)
Infection and tissue rejection
Hernia recurrence due to mesh failure
Nerve damage or burning sensation
Organ perforation
These complications often require revision surgery, which may involve mesh removal, further recovery time, and long-term health risks.
You may be eligible if:
You had hernia repair surgery on or after January 1, 2013
You received a Covidien, Bard, Atrium, or Ethicon mesh implant
You experienced serious complications or needed revision surgery
You have medical records showing mesh-related injuries
You file your case within the statute of limitations in your state
Even if another firm previously declined your case, we may still be able to help.
Thousands of hernia mesh lawsuits have been filed across state and federal courts, with key verdicts and settlements including:
$1 Billion Bard Settlement (2024): Covered 38,000+ claims in RI and Ohio MDL
$500,000 Verdict (2023): Ohio man suffered from PerFix Plug complications
$4.8 Million Verdict (2022): Rhode Island man injured by Bard’s Ventralex mesh
$255,000 Verdict (2022): Bowel abscess caused by mesh adhesion
$66 Million Settlement (2021): Resolved 3,000+ Atrium C-Qur lawsuits
$180 Million Settlement (2011): Kugel Patch lawsuits over bowel and organ injuries
These outcomes reflect the seriousness of hernia mesh complications and the potential compensation available to victims.
The FDA MAUDE database has documented adverse events involving:
Covidien Parietex Surgical Mesh
Covidien Parietex Composite Mesh
Covidien Parietex ProGrip Mesh
Reports include chronic pain, debilitating groin pain, infections, and multiple surgeries to remove defective mesh.
Despite growing concerns, no official recall has been issued by Covidien or the FDA — though the agency has acknowledged risks like:
Pain and hernia recurrence
Adhesions and obstructions
Mesh shrinkage or migration
At SSKB, our medical device litigation team has the experience and resources to take on large corporations like Covidien, Medtronic, and Johnson & Johnson.
We will:
Confirm your eligibility through a free case review
Collect evidence including medical records and surgical history
Handle all legal filings and meet crucial deadlines
Negotiate the highest possible settlement
Take your case to trial if needed
We charge no upfront fees — we only get paid if we win your case.
A successful hernia mesh lawsuit may provide compensation for:
Medical expenses (past and future surgeries)
Pain and suffering
Lost wages or loss of earning potential
Emotional distress
Reduced quality of life
In cases of severe complications, you may also be eligible for punitive damages.
Q: Has Covidien recalled their hernia mesh products?
A: Not at this time. While there is no formal recall, the FDA has acknowledged reported complications. Multiple lawsuits are underway.
Q: What if my surgery was years ago?
A: As long as you had surgery after 2013 and are within the statute of limitations, you may still qualify.
Q: Do I need to know the brand of mesh used?
A: Not necessarily. Medical records will show the manufacturer and type of mesh used in your surgery.
Q: What if I was previously denied by another firm?
A: SSKB is reviewing declined and discharged cases. We may be able to help where others could not.
If you or a loved one suffered complications from a Covidien or other hernia mesh device, don’t wait. Let us help you pursue the justice and compensation you deserve.
📞 Call (800) 675-8556
📨 Or fill out our secure contact form for a free, no-obligation consultation