Our hernia mesh lawyers seek new clients suffering severe side effects from these defective products. Over 25,000 hernia mesh lawsuits have been filed, and over 24,000 in the Bard litigation alone.
Three hernia mesh device lawsuits have gone to trial, and a settlement for Bard cases may be coming soon. Our hernia mesh lawyers provide the latest news and updates in the hernia mesh class actions below, as well as predictions about the potential settlement payouts in these cases.
Our firm is still taking new hernia mesh lawsuits even after the settlement. Reach out to us online to see if you have a viable claim or call 800-553-8082.
Hernia Mesh Class Action Lawsuit News and Updates
Before we discuss projected hernia mesh settlement amounts, let’s update you on the latest developments in the hernia mesh lawsuits.
October 1, 2025 – Case Counts
Bard now has 24,004 lawsuits. This combines settled cases with opt-out claim. Once these settlements start getting processed, this number will drop dramatically.
The Covidien cases are continuing to heat up and there are now 2,152 cases as they head into their first trial in January.
September 22: We ARE Taking New Bard Claims
Not many lawyers are still taking these cases post-settlement. We are. If you want to bring a claim, we could be at the now or never point in terms of finding a lawyer.
If you want to talk to us about bringing a claim, call us at 800-553-8082 or submit an online contact form.
September 10, 2025 – Bard and Covidien Case Counts
There are now 24,026 cases in the MDL, so basically no change from last month. Bard hernia mesh is the second largest federal MDL in the country.
The Covidien litigation now has 2,090 cases as those claims head towards a bellwether trial early next year.
August 14, 2025 – Covidien MDL Trial Track
The Covidien MDL is now in a pressure cooker phase. Patterson v. Covidien, the first federal bellwether, is locked in for jury selection on February 17, 2026, with a pretrial conference in Boston scheduled for February 4. The joint pretrial memorandum is due January 27.
This timeline is aggressive, especially given the depositions and expert disclosures still in progress. The courtroom pressure is mounting just as state court dockets in Massachusetts and Minnesota gain momentum. Covidien now faces multi-front exposure, with the federal MDL and state cases coalescing into a unified litigation threat.
August 7, 2025 – Bard MDL Case Count
Despite last year’s settlement announcements, the Bard hernia mesh MDL continues to generate new activity. As of August 1, there are approximately 24,029 active cases pending in the Southern District of Ohio.
While that number reflects a modest decline from earlier highs, it is a far cry from a wind-down. New cases are still being filed and the claim review process remains ongoing.
This MDL is not in its final chapter. It is stuck in a prolonged settlement administration phase with many plaintiffs still waiting for real compensation before agreeing to settle.
August 2, 2025 – Bard Settlement Fund Established
The settlement infrastructure is finally taking shape in the Bard MDL. Orion Settlement Solutions has been appointed to administer the qualified settlement fund for claimants. This means lien resolution, payment allocation, and individual awards are now inching closer to reality.
But, sadly, “closer” is doing a lot of work here. Realistically, many plaintiffs will still be waiting into 2026 or beyond for actual payments to land. This is the slow churn of mass settlement resolution in full view.
July 14, 2025 – Covidien MDL Case Volume Expands
The federal Covidien MDL now has just over 2,040 pending cases. That number alone is significant, but it only tells part of the story. Massachusetts state court is handling over 6,000 additional Covidien mesh cases, with another 500 pending in Minnesota.
A first trial in Massachusetts is scheduled for fall 2025. That state track might be where real pressure is applied if Covidien believes the federal MDL can be stalled through procedural maneuvering. But the convergence of these tracks suggests the company will not have the luxury of delay for long.
June 18, 2025 – Key Covidien Deposition Scheduled
A major deposition in the Covidien litigation is scheduled for July 17. The deponent is one of the original inventors of a disputed mesh product. Plaintiffs are betting this testimony will strengthen the core narrative of defective design and known risk. If the deposition delivers what plaintiffs hope, it could reshape the evidentiary posture ahead of the February bellwether.
June 1, 2025 – Bard MDL Sees Surge
The Bard MDL is still growing. We are now up to 25,015.
May 1, 2025 – Bard MDL Update
The Bard hernia mesh MDL in Ohio added 411 new cases this past month, bringing the total to 24,078. That is the biggest single-month increase in half a year—something you do not usually see after a global settlement.
April 11, 2025 – Covidien Bellwether Trial
The Covidien hernia mesh litigation is finally heading toward its first jury trial. On April 8, Judge Saris set a clear timetable for the first bellwether case in the federal MDL, with trial scheduled to begin on February 17, 2026. A pretrial conference will take place in Boston on February 4, and the joint pretrial memorandum is due January 27.
This case, if it actually goes to trial, will shape the future of the litigation. The plaintiff in this case claims the Covidien Symbotex mesh implanted in 2017 caused severe adhesions and bowel obstruction after the mesh’s protective collagen layer broke down prematurely. Patterson required a small bowel resection and further surgery to remove the device—exactly the type of failure at the core of many mesh claims.
This is more than just one trial. It is a test of jury perception, corporate exposure, and the viability of Covidien’s defenses. Recent settlement negotiations did not yield a resolution, but these early trials may finally move the needle. If no resolution follows the bellwethers, hundreds of cases could be remanded for trial across the country. The pressure is mounting on Covidien to come to the table.
April 4, 2025 – Update on MDLs
As of April 1, 2025, the Bard hernia mesh multidistrict litigation (MDL) had 24,080 pending cases—a decline from the total reported two months earlier. This reduction aligns with the ongoing settlement finalization process. In comparison, the Atrium hernia mesh MDL currently has 436 pending cases, while the Covidien hernia mesh MDL reports just over 1,700 cases still awaiting resolution.
February 20, 2025 – Settlement Talks Possible on Covidien
Mass tort litigation can take years to reach resolution, and the ongoing litigation involving Coviden mesh is no exception. Plaintiffs have been seeking justice for years. Now, the Covidien litigation appears to be reaching a crucial juncture. Both sides have agreed to extend the deadline for selecting a mediator to February 24, 2025, indicating that maybe—just maybe—settlement discussions are gaining traction. This extension provides additional time for negotiations on a neutral third-party mediator—a key step in determining whether a resolution can be reached without more protected litigation and bellwether trial.
Past mass tort cases show that settlements often come after years of legal wrangling and just before the risks of trial become too great. This could be a pivotal moment in the Covidien litigation. If the pattern holds, now may be the best opportunity for resolution before the case proceeds to costly bellwether and risky trials. The Bard cases have settled. It is time for Covidien.
January 25, 2025 – How Many Will Take Quick Pay?
January 17, 2025 – Dealing With Medical Liens in the Bard MDL
How are liens going to be handled in the Bard settlement? Plaintiffs’ Lead Counsel has Archer as the exclusive lien administrator to identify and resolve various liens or subrogation interests, including those related to Medicare, Medicaid, TriCare, and Veterans Affairs.
To facilitate this process, the court authorized the release of protected health information to Archer, ensuring compliance with the Health Insurance Portability and Accountability Act of 1996 (HIPAA). Archer is required to maintain the confidentiality of this information and use it solely for lien resolution purposes. The order also specifies that any third parties assisting Archer must adhere to the same confidentiality standards.
January 8, 2025 – MDL Judge Considers Proposals for Bellwether Schedule
This week, attorneys for both sides submitted separate proposals to the MDL judge outlining plans for the Coviden bellwether trial process. The plaintiffs’ proposal suggests selecting a group of 16 cases by February, preparing them for trial, and beginning the first trial in September 2025. In contrast, the defendants’ proposal outlines a more complex case selection process, pushing the first bellwether trial to sometime in 2026. The MDL judge will now determine whether to adopt one of these proposals or establish her own schedule.
December 1, 2024 – Opting Out of the Hernia Mesh Settlement
We have been saying there will be opt-outs of the Bard hernia mesh settlement. How will that work?
The short answer we learned in Case Management Order No. 55 is that it will take a very long time. Mediations for opt-outs will not be until January 2027.
That seems like a long way way. But if there is still no settlement, you cannot opt out and push for a trial scheduling until June 2029. So you might not see another trial for an opt out until 2030… or later.
For plaintiffs already grappling with health complications and financial hardships caused by defective hernia mesh products, these delays will likely feel like justice deferred—and most victims will understandably view this justice delayed as justice denied.
October 23, 2024 – Some Settlement Details
Some settlement details are coming out:
- The settlement program will take 3-4 years to administer, and payments will be made based on the order lawsuits were filed, meaning earlier cases will be paid first.
- A quick pay option offers a fixed settlement of $25,000 for claimants with straightforward cases (e.g., single surgery, less severe injuries). A smaller payment of $2,500 is available if Bard mesh was not deemed the cause of injuries. Otherwise, there is a more with potential higher payouts based on the severity of injuries. Payments will likely take 2-4 years to be distributed.
- There is the ability to opt-out of the settlement. But the form that will take remains to be seen.
October 14, 2024 – How Settlement Might Work
I don’t have any more details other than more rumor and speculation. So let’s talk generally how I think the Bard settlement will work.
If history is an guide, we will have a settlement points system in the Bard hernia mesh lawsuits to determine compensation amounts per person.
This system will assign points based on several factors, starting with the severity of injuries, such as chronic pain, mesh failure, or organ damage. More points will likely be awarded to plaintiffs who required multiple surgeries or suffered permanent disability. Other factors, such as lost wages, diminished earning capacity, or other objective factors of diminished quality of life should further increase the settlement point totals. Conversely, deductions will likely apply for complicating factors, such as pre-existing conditions.
The system will try—and inevitably fail—to get consistency in the numbers while properly accounting for individual variations, with higher settlements for more serious lawsuits. The reality is that a algorithm can never do this.
Again, I have been saying an per person average of $65,000 or $70,000 is my best guess. If you are a plaintiff, you are hoping as I suspect, that there are a lot of weak cases filed in the MDL. Why? Because that will push the average down meaning that cases were there was meaningful suffering will be higher than this average.
October 3, 2024 – Settlement Rumors
I’m hearing rumors of $65,000 average settlement and up to five years for payouts in some cases. The latter is not a unanimous sentiment.
October 2, 2024 – Bard Hernia Mesh Settlement
We have—finally—a Bard hernia mesh settlement. We do not know much except that it will resolve the “vast majority” of claims. The deal appears to have been strung out, at least for some plaintiffs, for years (“aggregate amount payable pursuant to this settlement is within the company’s current product litigation reserve for this matter and will be paid out over a multi-year period”).
We will have more information in the days and weeks to follow and will keep you posted on what we know.
October 1, 2024 – MDL Updates
In the past month, more than 100 new cases were added to the Bard hernia mesh class action MDL. Additionally, 41 cases were added to the Coviden MDL, raising its total number of cases to 1,511.
September 26, 2024 – Covidien MDL Progress; No News in Bard
The Covidien hernia mesh litigation is making significant headway, with nearly 1,500 lawsuits currently pending. Plaintiff attorneys have been busy deposing key witnesses from Covidien as part of a thorough discovery process aimed at uncovering critical evidence to strengthen their cases. Both parties remain actively engaged in this phase, with expert testimony expected to follow once fact discovery concludes later this year.September 17, 2024 – Judge Denies Motion to Remand
Yesterday, Judge Edmund Sargus denied a motion for remand filed by plaintiffs frustrated with the slow pace of settlement negotiations. The motion was denied without prejudice due to a limited stay in the case, as outlined in Case Management Orders 52 and 53, which restrict filings, including remand requests, apparently, during this period.
The decision was expected. You would have seen a flood of motions to remand if the motion was granted. But victims are growing tired of his holding pattern in the litigation and it is hard to blame them.
September 3, 2024 – Updated MDL Totals
The active hernia mesh MDLs continue to grow with new cases added each month. The Covidien hernia mesh MDL currently has 1,472 pending cases, while the Bard MDL has just over 24,000.
August 8, 2024 – New Bard Cases Still Getting Filed
Even as global settlement negotiations get closer to conclusion, new hernia mesh cases are still being filed in the Bard MDL. One of the most recent cases was filed by a man from Nevada. The complaint states that he had the Bard Ventralex Hernia Patch implanted back in 2010 and that complications caused by defects in that patch have resulted in subsequent corrective surgeries.
August 5, 2024 – Covidien MDL
While we wait for the Bard settlement to be finalized, it does not look like Covidien will settle anytime soon. From July to August 2024, the Covidien Hernia Mesh Products MDL saw a slight increase in active cases. In July 2024, there were 1,322 active claims, which increased to 1,410 in August 2024. This reflects an addition of 88 active lawsuits over the month.
July 9, 2024: Waiting
No other additional information has been provided on the settlement agreement. We are just waiting to see what is in it and more details on how it will work for victims who do not want to participate.
July 6, 2024: Master Settlement Agreement
Two new court orders published yesterday reference a Master Settlement Agreement. We do not have any more details, but a global settlement is becoming a reality.
July 1, 2024: Motion on Settlement Confidentiality Rejected; Settlement Rumors Continue
On Friday, two law firms with “several hundred” plaintiffs and Bard filed a motion in the Bard MDL to seal the terms of their hernia mesh settlement with Bard. Today, the court rejected the motion, emphasizing that the public has a strong right to access court records. To seal a document, there must be very strong reasons, which the parties have not provided, the MDL judge said. The Court has previously ruled that claims of potential prejudice are insufficient to justify sealing.
What we have been telling you is that some firms have settled out with Bard. All that has been under wraps until this motion broke the silence. This is in the midst of A LOT of rumors of a global settlement is on deck.
June 19, 2024: Study on Robotic Hernia Repairs
A research study published in a major medical journal this week reports that people who opt for robotic hernia repair surgeries are much more likely to have their hernia reoccur compared to those who undergo traditional procedures.
June 3, 2024: 640 New Cases
The Bard Hernia Mesh class action MDL is still expanding rapidly. In May alone, 640 new hernia mesh cases were added, surpassing last month’s increase. This brings the total number of pending cases to 22,896.
May 30, 2024: Bard Mesh Lawsuits Continue Getting Filed
Lawyers continue to file Bard hernia mesh lawsuits. In a newly filed case in the MDL this week, a resident of Puerto Rico sues alleging his Ventralex ST Patch implanted in 2020 was defective.
May 1, 2024: Continued High Volume in MDL
The volume of new cases in the Bard hernia mesh class action MDL continues to be very high. 583 new cases were added to the Bard hernia mesh MDL during the month of April. That is more than the 481 new cases added last month and it brings the total number of pending cases up to 22,256.
April 23, 2024: Quiet Docket
There has not been a peep on the Bard MDL docket in the last 11 days. All I have for you is rumors expressing optimism. Nothing else.
April 1, 2024: Over 400 New Cases Added to Bard MDL
Over the past month, the Bard hernia mesh class action MDL saw an addition of 411 new cases, bringing the total number of pending cases to 21,673. This also signifies the highest monthly influx of new cases observed in the Bard MDL in the last six months.
March 1, 2024: MDL Adds 100 More Cases
There are now 21,262 total cases pending in the Bard hernia mesh class action MDL. Around 100 new cases were added to the MDL just last month. The size of the MDL continues to make a global settlement deal difficult.
February 20, 2024: Settlement Mediation Is On
In the never-ending saga of the polypropylene hernia mesh litigation, Judge Sargus scheduled a mediation scheduling order.
The judge’s order schedules a settlement mediation for March 4 and 5, 2024. The settlement will be in person. This step – presided over by the court-appointed mediator, John Jackson – is at a critical juncture in the proceedings. There are no more bellwethers. All we have left is a remand for trials all over the country. That said, the contours of the settlement dynamics appear largely the same as they were in November.
The order’s provision for a notification deadline by May 24, 2024, in the event of an impasse, followed by a June 24, 2024, deadline for submitting a joint proposal on how to proceed, reminds of the measured approach Judge Sargus has taken throughout this litigation.
There is real hope for this settlement mediation because it just feels like all of this has gone on long enough. Hernia mesh lawyers are tired and, more importantly, victims are tired. But this for this settlement mediation is tempered by the fact the dynamics at play remain too reminiscent of past negotiations. My fear, and I want to be proven wrong, is that without trial dates all over the country, Bard is not feeling enough pressure to get reasonable settlement amounts from it.
February 6, 2024: Fourth Bellwether Trial Is Off
The MDL judge cancelled the Byran trial coming up in April and is not replacing it and not remanding the cases for trial in their original jurisdictions. Instead, the court seems to be saying get these lawsuits settled.
The sentiment is great. But these cases have not settled with the pressure of trial dates. It hard to imagine they will settle without the pressure of trial dates.
February 1, 2023: 100 More Cases Added to MDL
Nearly 100 new cases were added to the C.R. Bard hernia mesh class action in the month of January. That brings the total number of pending cases up to 21,169.
January 15, 2024: 20,973 Cases in Bard MDL
As we head into the new, the C.R. Bard hernia mesh class action MDL has 20,973 pending cases. It is still the largest of the hernia mesh MDLs.
November 13, 2023: More Bellwether Trials Set
What is next in the hernia mesh lawsuits? Another trial. Scheduled for January 2024, the fourth/fifth bellwether trial involving Bard centers on plaintiff Jacob Bryan, who underwent a surgical procedure involving the use of a 3DMax hernia mesh for inguinal/groin hernia repair. Post-surgery, Mr. Bryan experienced severe complications, including mesh deformation and chronic pain, which have necessitated ongoing medical treatment and may lead to additional surgery.
Originally selected as a bellwether trial by the defendants years ago, there was an effort by them to remove Mr. Bryan’s trial date. Their argument centered on the premise that Mr. Bryan’s complications were more severe than initially expected, potentially skewing the representative nature of the bellwether trial. However, the motion to replace Mr. Bryan as a bellwether case was denied by the Judge Sargus.
The product at the center of this case, the 3DMax hernia mesh, is subject to similar allegations as other products in similar lawsuits. The plaintiff accuses Bard of failing to adequately warn both patients and healthcare providers about the significant risks and potential complications associated with the use of the 3DMax mesh. This includes not just an omission of known risks but also underrepresentation of the severity and frequency of possible adverse effects. Additionally, the lawsuit raises issues regarding the design and manufacturing of the 3DMax mesh. It is alleged that defects in the design and manufacturing process contributed to the complications suffered by patients like Mr. Bryan.
November 9, 2023: We got a verdict yesterday: $500,000.
The jury found for Bard on design defect but found for the plaintiff on the failure to warn case. All along, we have been saying this case is about failure to warn. This verdict underscores that belief.
No punitive damages were awarded.
Let’s recap the verdicts now:
Plaintiff Date Venue Award Johns July 2021 MDL $0 Milanesi April 2022 MDL $250,000 Trevino August 2022 Rhode Island $4,800,000 Stinson October 2023 MDL $500,000
November 8, 2023: On Day 14 of the Stinson bellwether hernia mesh trial, Bard called brought Dr. Stephen Badylak to the stand, a witness with a history of testifying for Bard in similar cases. In a move reflective of the parties confidence in a favorable outcome, both sides have jointly filed a motion advocating for the use of a single damages’ verdict form, a measure in accordance with Maine law. This is intended to minimize confusion among jurors and reduce the risk of potential appeals or retrials due to the issue of multiple recoveries for a single harm.November 1, 2023: Yesterday was entirely focused on Dr. Pomerants’ testimony, which included continued direct questioning, cross-examination, and then a redirect.
October 31, 2023: Plaintiff rested his case yesterday.
October 27, 2023: We said Dr. Grischkan was a key witness. All day yesterday was spend on his continued testimony.
October 26, 2023: Today is Day 9 of the Stinson trial. Yesterday, the plaintiff and David Grischkan provided testiomony. Dr. Grischkan is a board certified general surgeon who specializes in the repair of abdominal wall and inguinal hernias. He is a key plaintiff’s expert on specific causation.
Let’s take a second and recap the allegation in Stinson. The main argument from the Plaintiff is that Bard was aware of the risks associated with its PerFix Plug device but still promoted and sold it without properly warning doctors and patients.
What was the problem? Plaintiff design defect claim contends that the PerFix Plug breaks down after being implanted, leading to a prolonged inflammatory reaction in the body. So instead of putting a warning on the product giving doctors the information they need to do a risk/benefit analysis, Bard minimized the potential complications of the device, patients at an undue risk of severe and lasting harm.
Plaintiff’s lawyers also argue that this inflammatory reaction is exacerbated by poor design choices in the device’s shape, weight, and the size of its pores.
October 17, 2023: The size of the Bard hernia mesh MDL actually decreased over the last month from 20,405 to 20,369 pending cases. This is the first time ever that this class action MDL has posted a monthly decrease in pending cases. What does this mean? It is difficult to say until we see if the trend continues, but this could be a sign that we are running out of possible plaintiffs.
October 10, 2023: The third bellwether trial is upcoming in the case of Stinson v. Davol, et al. The plaintiff in the case underwent a right inguinal hernia repair in 2015, during which he had a Bard Per-Fix Mesh implanted. For 2 years after the surgery, the plaintiff had chronic pain in the area. In 2017, he underwent exploratory surgery to determine if it was a recurrent hernia or nerve entrapment causing the pain. During this procedure, the surgeon found that the Bard mesh implant had curled up into a ball, causing major scarring on the internal tissue. The mesh was removed and replaced, but the plaintiff continued to have pain.
October 2, 2023: The third bellwether test trial is set to be in 2 weeks in the Stinson case. We could see this case settle before the trial actually happens, but in the meantime, the lawyers for both sides certainly appear to be gearing up for trial. Bard has filed numerous pretrial motions over the last 2 weeks, including a significant motion filed on September 29th seeking to limit the testimony of one of the plaintiffs’ experts.
September 23, 2023: The federal judge overseeing all Covidien hernia mesh lawsuits across the federal court system has approved a proposal from the plaintiffs. This proposal involves the preparation of a set of six bellwether cases, with two trial cases to be selected in early 2025. This litigation has moved slowly and 2025 is still a long way way. But this is progress. Getting trial dates is the key to getting reasonable settlement offers.
There are 641 hernia mesh lawsuits in the Covident MDL class action lawsuuit. These lawsuits all contend that a faulty design in Covidien Parietex, Covidien Symbotex, and others, has led to unnecessary pain and suffering. In most of these cases, the plaintiff was required to get more surgery to fix the problems caused by the defect.
September 14, 2023: The pace of new cases in the Bard hernia mesh class action MDL has slowed somewhat this summer. There are currently 20,405 pending cases in the MDL. At the start of the summer there were 19,707 pending cases. 250 cases per month is still significant, but its way less than the monthly volume we were seeing in this class action earlier this year.
September 1, 2023: After a very long wait, it looks like the next bellwether test trial in the Bard hernia mesh MDL is finally going to happen. In a new Case Management Order issued yesterday, the MDL Judge confirmed that trial in the case of Stinson v. Davol, Inc., et al. (18-cv-1022) will begin on October 16, 2023. A fourth bellwether trial will be scheduled for early 2024 in the case of Bryan v. C.R. Bard Inc., et al. (18-cv-1440).
August 16, 2023: The Bard MDL has been frustratingly quiet in August. The MDL did add 191 new cases last month, increasing the total case count for the 3rd largest MDL in the country to added to 20,126 lawsuits.
August 10, 2023: The pivotal 3rd bellwether test trial is on track to begin on October 16, 2023 in the case of Stinson v. C.R. Bard, et al. (2:18-cv-01022). In preparation for that upcoming trial, the MDL Judge recently issued an Order setting last-minute discovery deadlines related to the plaintiff’s post-operative treatment last month. The order gives the parties until August 14, 2023, to complete supplemental fact depositions and until September 27 to finish additional expert depositions. The short time frame of these deadlines suggests that the judge is committed to going to trial in October without further delays.
July 18, 2023: As we inch closer to the long-anticipated 3rd bellwether trial, new hernia mesh lawsuits continue to get transferred into the C.R. Bard class action MDL. Over the last month, 228 new hernia mesh cases were added to the MDL. That brings the total number of pending cases up to 19,935, making MDL 2846 the 3rd biggest consolidated mass tort behind 3M earplugs and Talcum Powder.
July 15, 2023: No reasonable person can suggest that hernia mesh implants have not been wrought with controversy and complications. The FDA is trying to help guide patients and doctors about the benefits and risks of utilizing surgical mesh for hernia treatment. This week, it put out a new guide that offers a detailed overview of the pros and cons of surgical mesh.
July 7, 2023: Plaintiff’s lawyers withdrew its manufacturing defect claim in Stinson. This narrows down the issues for trial. These cases will always be focused on the failure to warn.
June 30, 2023: This litigation is now focused on Stinson, as you can see from most of the recent updates. Defendants filed a motion for summary judgment, making its usual arguments. Plaintiff has until Wednesday, June 14, 2023, to file a response.
June 13, 2023: Judge Sargus ruled that the mesh used in Aaron Stinson’s surgery did not come from the Puerto Rican factory and was manufactured four years later. So Stinson’s lawyer cannot present what the court says is unrelated evidence to establish a general pattern of unsafe conduct, as per federal rules of evidence. Stinson alleges that the PerFix Plug mesh caused scarring, subsequent surgery, and ongoing complications.
Is this a big deal? It is not. This is not a big part of the plaintiff’s case in Stinson.
June 4, 2023: We have been telling you that Stinson’s next bellwether trial is the best case yet for defendants. The first two bellwether trials were more challenging cases for plaintiffs, arguably not representative cases because of the weaknesses in those cases that came out throughout pretrial discovery.
Naturally, Bard now claims that Stinson’s case has evolved medically to the point where he no longer represents the majority of the claims for bellwether purposes. Their fear is another significant verdict will escalate the settlement amounts Bard will have to pay in a global settlement. Conveniently, it ties in nicely with Bard’s “delay, delay, delay” tactic: to hold on to their money as long as possible while hoping the endless delays force plaintiffs to take lower compensation payouts. If the judge agrees to delay Stinson, there would be more delay to get the next case ready for trial.
June 1, 2023: A state court judge in Rhode Island made an interesting ruling in the post-verdict motions in the Trevino case. Justice Richard A. Licht of the Providence Superior Court remitted $250,000 of a disfigurement award while leaving $4.55 million intact. It seems like an odd place to draw a line, right? More importantly, the ruling confirmed that Bard could be liable under Rhode Island’s warning requirements, and there was sufficient evidence to support the failure-to-warn claim.
May 11, 2023: One issue the court wants to address in the Stinson trial is whether, under Maine law, manufacturers of medical devices hold an ongoing responsibility to inform patients (via their doctors) about any risks associated with a medical device that has already been implanted, especially if these risks are identified after the device has been implanted.
The parties are instructed to provide additional briefing by May 17, 2023.
May 5, 2023: The third MDL bellwether trial date, Stinson v. C.R. Bard, has now been rescheduled. The new date for the trial is set for October 18, 2023.
May 1, 2023: Settlement talk remains in the air, but losing the trial date in Stinson did not expedite settlement efforts.
March 22, 2023: The highly anticipated third bellwether test trial (Stinson v. C.R. Bard et al.) in the C.R. Bard hernia mesh class action MDL is now rescheduled for October 16, 2023. The trial was supposed to begin next month, but the MDL Judge granted a request by the defense to push the trial back. The first bellwether trial yielded a defense verdict, and the second test trial resulted in a modest $250,000 verdict. But in August 2022, a hernia mesh trial in Rhode Island state court ended in a $4.8 million verdict.
March 20, 2023: The third bellwether trial in the C.R. Bard hernia mesh MDL has been postponed. The case of Stinson v. C.R. Bard was supposed to go to trial on May 15, 2023, where it would serve as the third test case. Last week, the MDL judge denied a summary judgment motion by the defense, clearing the way for the Stinson case to proceed. Two days later, however, the Judge granted Bard’s defense team a request to postpone the upcoming trial date. No new trial date has been set.
Summary of Hernia Mesh Defects
A hernia is a very common medical condition that must be surgically repaired. Almost 1 million hernia repair surgeries are performed at hospitals in the U.S. every year, making hernia repairs the most common type of surgical procedure in modern medicine. Over the last 20-30 years, most hernia repairs have used a mesh or patch implant device. These devices most typically treat:
- Incisional Hernia: weakness in the muscle of the abdomen
- Ventral Hernia: weakness specifically in the abdominal wall muscles
- Femoral Hernia: upper thigh or outer groin
- Inguinal Hernia: inner groin
- Umbilical Hernia: a bulge that forms at the belly button
- Hiatal Hernia: stomach bulges up into your chest
When performing hernia repair surgery, doctors tuck the protruding organ (usually an intestine) back into place and surgically repair the muscle wall that holds it in place.
A mesh or patch is like a tiny net or screen the surgeon implants in or around the repaired muscle tissue. The surgical mesh has biological materials. This allows connective tissue to develop that acts as structural support to strengthen and reinforce the repaired muscle wall at the hernia site. The muscle tissue regrows around the mesh or patch.
Because these devices are implants, they must be made out of inert materials that can exist inside the human body without triggering an immune system response. They also need to stay intact to not move or protrude into adjacent tissue after the surgery.
Most of the earlier mesh products were non-permanent/absorbable. They were made out of animal byproducts designed to be gradually absorbed by the body and disappear after implantation. These absorbable devices had a good safety record but did not provide permanent abdominal wall support.
In the early 2000s, a new wave of permanent hernia mesh devices from various manufacturers began to hit the market. These devices were made out of a particular type of plastic, surrounded by some type of inert coating material that was supposed to make them bio-compatible inside the body. Unfortunately, many of these new permanent mesh/patch implants had significant design flaws. These flaws led to chronic pain and other disastrous consequences for many patients, including a revision hernia mesh surgery.
Adverse event reports from healthcare professionals to the U.S. Food and Drug Administration grew. Eventually, and arguably belatedly, the FDA issued safety warnings and demanded product recalls.
The fundamental problem with this type of hernia mesh is its biocompatibility inside the human body. Instead of being inert once implanted in the body, the permanent mesh devices had design or manufacturing issues that caused these synthetic materials to be incompatible with the human immune system.
Once implanted, the defective hernia mesh devices would trigger an immune system attack, resulting in inflammation and other complications. Another related problem is that their outer coating degraded too quickly, causing the mesh to become abnormally attached to internal organs or tissue.
Injuries Caused by Hernia Mesh Defects
The defective hernia mesh devices can cause internal injuries and/or health complications. The most common injuries linked to defective hernia mesh products:
- Internal infections and pain
- Bowel obstruction
- Mesh detachment and migration
- Puncture of adjacent tissue/organs
- Fistula formation
- Abscess formation
- Adhesion to other organs or tissue from scar tissue formation
Many of these complications require additional surgery to repair or correct.
In some cases, hernia repair surgery patients started experiencing some of these complications within just a few days after the mesh was surgically implanted. For others, however, there was a substantial delay between the hernia surgery and the onset of symptoms related to defects in the hernia mesh device.
Do I Qualify for a Hernia Mesh Lawsuit?
Our law firm is accepting new hernia mesh cases from anyone who meets the following basic criteria:
- You had a hernia repair surgery sometime in the last 15 years, AND a hernia mesh device was implanted.
- You experienced complications or injuries related to hernia mesh implant device defects.
If you or a family member meet these criteria, CONTACT US.
How Do I Know If My Hernia Mesh Has Failed?
When a hernia mesh implant fails, it can trigger several acute physical symptoms, including
- abdominal bloating or discomfort
- constipation or bowel blockage
- fever
- nausea and vomiting
- hernia recurrence
- pain and swelling.
In most cases, these physical symptoms will be severe enough that the patient will seek medical attention. This is usually when the failure of the hernia mesh implant is identified.
Hernia Mesh Lawsuits Medical Studies
The key to success for victims in the hernia mesh litigation at the settlement table and trial is the strength of the scientific and medical literature that underscores the risk of mesh implants. These are some of the critical studies at issue in the litigation.
- Dong, Z. et al. “Does using hernia mesh in surgical inguinal hernia repairs cause male infertility? A systematic review and descriptive analysis.” Reproductive Health. 15.1 (2018): 1-14. (This study looked at the association between hernia meshes and male infertility. The researchers looked at 29 related trials. They found that hernia mesh repairs, open and laparoscopic-assisted, did not negatively affect male fertility. This nixed any claim in this regard in the hernia mesh lawsuits.)
- Gachabayov, M., et al. “Recurrence of infection and hernia following partial versus complete removal of infected hernia mesh: a systematic review and cohort meta-analysis.” Hernia. 24.3 (2020): 433-439. (This meta-analysis and systematic review compared infection and hernia recurrence rates in partial and complete hernia mesh removals. Infection recurrence rates were 59 percent in partial removals and 26 percent in incomplete removals. Hernia recurrence rates were about 10 percent in partial removals and 40 percent in incomplete removals. The researchers concluded that partial removals increased the infection recurrence risk, while complete removals increased the hernia recurrence risk.)
- Ilyashenko, V. V., et al. “Laparoscopic management of large hiatal hernia: mesh method using ProGrip mesh versus standard crural repair.” Surgical Endoscopy. 32.8. (2018): 3592-3598. (This study compared and contrasted the effectiveness of laparoscopic-assisted hernia mesh repairs and crural repairs. The researchers concluded that hernia mesh repairs were “effective and durable” for an extended period.)
- Raj, P.P., et al. “Morbid obesity with a ventral hernia: is concomitant bariatric surgery with laparoscopic ventral hernia mesh repair the best approach? An experience of over 150 cases.” Surgery for Obesity and Related Diseases. 15.7 (2019): 1098-1103. (This study examined whether combining bariatric surgery with an intraperitoneal hernia mesh repair was the best treatment for obese patients with ventral hernias. The researchers concluded that bariatric surgeries with intraperitoneal hernia mesh repairs could treat obesity and hernias without significant risk of recurrence.)
- Sandø, A., et al. “Long-term patient-reported outcomes and quality of the evidence in ventral hernia mesh repair: a systematic review.” Hernia. (2020): 1-11. (This study looked at whether patient-reported outcomes changed three months after a ventral hernia mesh repair. The researchers found patients who underwent sizeable incisional hernia mesh repairs experienced pain and physical impairment.)
Get a Lawyer for Your Hernia Mesh Lawsuit
If you have a potential hernia mesh implant lawsuit and want to discuss the potential value of your claim, contact a hernia mesh attorney at Miller & Zois for a free consultation. Three things to know:
- You pay nothing unless you get compensation.
- You will not get a hard sell from us. Just information and help if you want it.
- Our law firm has spent the last 20 years fighting exclusively for injury and wrongful death victims.
Call a hernia mesh lawyer today at 800-553-8082 or submit an online contact form.