Monday, June 01, 2026

 

Subject: CRITICAL: Constitutional Conflict in Election Disclaimer Mandates (IC § 3-9-3-2.5)
Chairman,
As a GOP candidate for Marion County Clerk, I am reaching out regarding a major legal liability embedded in Indiana election law.
Indiana Code § 3-9-3-2.5 enforces compelled disclaimers on political printing. This statute is unconstitutional under a mountain of settled U.S. Supreme Court precedents—including Talley, McIntyre, Buckley v. ACLF, and the recent Chiles v. Salazar decision.
Furthermore, the federal ruling in Majors v. Abell left the Indiana state constitutional claims completely unresolved, meaning our current enforcement structure sits on a legal cliff. It exposes county election boards and the state to massive federal lawsuits and damages under Monell and Section 1983, specifically concerning pure electoral slogans like those previously litigated in Stewart v. Taylor.
I have drafted a formal request for an Official Attorney General Opinion (AGO) focused strictly on independent Indiana state constitutional claims (Articles 1 and 2). This will force the AG to evaluate the law before a costly federal lawsuit is filed.
Because I am a candidate, I lack the statutory standing to submit this request directly. I need you, as Elections Chair, to sign this draft and submit it on your official legislative letterhead.
I have the complete, seven-question draft ready for your review. Please let me know where I can send the full text for your signature.
Respectfully,
[Your Name]
GOP Candidate for Marion County Clerk
[Your Email Address]

Representative Timothy Wesco Email: h21@iga.in.gov
Senator Mike Gaskill Email: Senator.Gaskill@iga.in.gov
You can now copy this text and close the tab. If you need any final address updates or routing numbers later, just ask when you are ready.

 

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  • Sunday, May 31, 2026

     tasks for monday

    beech grove city council 7 pm 9ish. have first ten letters mailed.  

    bring public record requests

    look for keys

    list budget schedule

    statement for cops:  

    michelle mighty jordan carlos other carlos tj zach mcvey 

    michelle was hospitalized anbd evicted but has noit been charged recently. she is a felon, a forger, a drug user, a thief embezzler and liar.

    she had hoped to have me civilly committed so she could get my house and funds. she is a former nurse, removed due to drug use and criminal activity.

     she had help in robbing me. jordan came to me offering to help me with my h h problem, but he was really there to steal. 

    j is cgararismatic, goodlooking, persuasive, hardworking, smart, determined, but a drug adduct, was wanted on a warrant for probabtion violation for armed robbery, a liar anbd thief, was dating michelle. she wnet after him with a baseball bat. he sends me fuck you letters from jail.  he has lost custody of his sons. he sent carlos to hassle us.

    racheal. racheal's boyfriends, the dead one, the drug addic tthief one. 

    we heard that kid died of diabetes. not josh, likelu od's at taco bell, but the cute thioefy one from southereastern.

    zach. zack was recently arrested driving the motorcycle he stole from me. peanut knows more. ab filled me in so trust but verify. zack trespassed here, allegedly stole michelle's phone to steal my credit card info, but that was mostly micghelle. zack night hace my stolen volvo in his dads garage zack had a stolen gun and drugs when he was arrested. michelle thinks he has clout e g might be a narc. zacj said to have rsperd a minor.  

    mighty is dennis washington jr. he threatened me, hit me, we fought, he threatened me again, he hit me very hard, he stole my wallet, used the cr4edit cards $1000. the prosecutor is avoiding me.  i've bene walked out of th ebuiding. i am functionally illeteratee. 911 hung up on me. cop at transist cetner re3fused to take report of gang activity, concealed identify iof victim's attacker. i called 911, they sent 3 cops, swat outfits, but they did not file a report. or  assign a detective. need to get those police reports again.

    collection agency is hassling me. i'll need to follow up w them. 

    5th 3trd is the bank tht is the problem.  

    wrinkle:  michelle was a client. i got her off a warrant in johnson county. she had told me we'd work together to expose corruption in johnson county, but it was all lies.  

    make list tof open cases:

    signs. marion county, me as plaintiff.

    johnson county greenwood bob. 

    h h 

    dog bite case

    alaska letter

    beech grove/hannah wrecker

    colorado letter 

     

     

    make list tof open cases:

    signs. marion county, me as plaintiff.

    meet w carla re campaign issues, access.  

    johnson county greenwood bob. 

    to do send letters requesting the policy to bob to the clerk, to the judge. 

    h h 

    change ownership of 4015. file motions. draft motions. let ai help. 

    fines: we won, but could still sue, lower priority.

    vote denial: file hava complaint prepare lawsuit. shop it around. 

    notices of tort claim. public records requests for who.  

    terre haute: church. pay 20k. get elecric. get wifi. visit. check progr4ess. look for keys, get locksmith. 

    dog bite case

    alaska letter

    beech grove/hannah wrecker

    colorado letter 

    clean front yard towards house. lost plates issue get cop contact, need paper from cop for lost plates. share rest opf story w cop.

    dustin? talk to re h h 

    dani get with. list budget schedule. her auto accidne thtiungy.

    needs referral. 

    mikle 13th emerson needs referral can we use his yard for a sign? stop the emerson boondoggle. vote stewart for clerk.  

     sherry has her stent thingy class action 

    doesnt qualify fo rfree vendoers permit?

    get p i license. pay the insurance. pay the fee, fill out the form.  

     

     

     

    Saturday, May 30, 2026

    Dear Todd,  

    Stop the Emerson boondoggle. Thank you. 

    Alias.

    Arbitrary Aardvark 

    Yo Senator Todd Youngster,  

    Until the federal budget gets balkanced and a plan is in place to pay poff the national debt, I request you urge yiour pal sean duffy to hold off on expneding funds for the merson boondoggle. We would like to see alternative budgets with less overall spoending and more local involvement, at least 1/2. 

    A pathetic Nunvoter. 

    Dear Governor Braun. Elections have consequences. Under Biden and Butigieg, the feds tried to funnel 17 million to a  Democratic mayor of a town in Indiuana. 

    That would have added to the national debt and the deficit, with no coresponding income stream such as a toll road or private sector investment would produce.   

    Help President Trump drain the swamp. Cancel this grant, or that is declaine to spend any state funds on this [project. Your adminstration should not be tainted with the Emerson boondoggle. Thanks. mark.  

     

    Emerson Avenue High Injury Network Safety Improvements

     

    BEECH GROVE, Ind. — Beech Grove has received a $17,082,400 grant to go toward improving safety along Emerson Avenue

    The grant is from the Safe Streets and Roads for All program.

    The city was awarded the grant for the "Emerson Avenue High Injury Network Safety Improvements," officials said, which will increase safety for drivers, pedestrians, cyclists and transit users along Emerson Avenue between Victory Drive and Main Street.

    "We knew it was a safety need for a long time," city engineer Andrew Wolf.

    City officials said there was one deadly crash and 32 serious injury crashes along Emerson Avenue between 2018-2022. 

    The grant will help the city convert four signalized intersections to roundabouts, close three median cuts and add raised medians and pedestrian refuge islands at 17 crossings. 

     

    A Wolf. A. Blinjken. A Dick.  

     

    The funding will pay for the majority of the City of Beech Grove’s Emerson Avenue High Injury Network Safety Improvement initiative. The project’s total price tag is $21.35 million.

    The City has indicated that its initiative “will boost safety for drivers, pedestrians, cyclists and transit users along Emerson Avenue between Victory Drive and Main Street.”

    Crews will do the following along Emerson Avenue during the project:

    • Replace four signalized intersections with modern roundabouts
    • = - = 
    • remove indent
    • now what if we built an app or say a mailijng list for people to write in to opose grant applications for any federsal money coming to indiana. we just start makiung sure every federal grant gets 100 letters against it. even if we have to buy them
    •  

     

     

      

     

    sherry use my name and attorney number

    need your medical records. 

    we could do an affidavit  w lydia

     

    Free Case Evaluation: 800-553-8082

    May 29, 2026

    Many of the new hernia mesh lawsuit filings this month have been in Rhode Island state court.

    May 4, 2026 – New Mesh Cases

    Our law firm is still taking new hernia mesh lawsuits after the settlement.  The total number of Bard hernia mesh trials is approaching 27,000.  The Covidien MDL has 2,396 as of May 1.

    Unlike many law firms, ours is still reviewing claims from victims.

    March 4, 2026 – Covidien Case Count

    Covidien is facing more than 2,200 hernia mesh lawsuits in the Massachusetts federal MDL before Judge Patti Saris. Many of the claims focus on mesh products such as Symbotex and Parietex, and plaintiffs say the materials can degrade, shrink, or trigger inflammatory reactions that lead to chronic pain, adhesions, infections, recurrence, and revision surgery.

    The first test case is finally coming (Patterson) in July. This case involves an Alabama man who says he got Symbotex implanted in 2017, later developed bowel adhesions and an obstruction, and then needed major corrective surgery in 2020 that included bowel resection, where the mesh allegedly stuck to his small bowel.  It is a pretty classic case in this litigation.

    Plaintiffs are finally getting what these MDLs often delay for years: a real jury trial. A bellwether does not bind the rest of the docket, of course, but it is the first time plaintiffs get to put the product, the corporate conduct, and the injury story in front of actual jurors. That matters because defendants can file motions and fight discovery forever, but a trial date forces a moment of truth. If the case is not resolved, a jury will decide whether this mesh is defective and what damages are appropriate.

    Covidien Hernia Mesh MDL: What Really Matters for Plaintiffs
    The core liability question Not whether complications happen with hernia repairs (everyone agrees they do), but whether specific Covidien mesh designs (especially polyester or composite configurations) create avoidable risks like adhesions, bowel involvement, shrinkage, chronic inflammation, infection, and recurrence.
    The injury story juries understand The most persuasive cases tend to be those with objective, surgical proof of harm, such as adhesions to bowel, obstruction, erosion, infection, fistula, or a revision surgery where surgeons document mesh involvement and removal is difficult or incomplete.
    The defense playbook Covidien will try to reframe every case as a “known surgical risk,” blame technique, patient factors, smoking, obesity, prior repairs, or infection unrelated to the mesh, and argue that any warnings were adequate. They also push hard on causation, especially in cases without a clean revision narrative. These may be a tough sell to a jury.
    The proof that moves the needle Plaintiffs gain leverage when records show a clear timeline: implantation → escalating pain or infection → imaging or hospitalizations → recurrence/obstruction → revision surgery documenting adhesions, shrinkage, or integration problems. Surgeon notes, pathology, explant analysis, and treating doctor testimony are often more persuasive than hired experts alone.
    Bellwether trial value The first bellwether is not binding on other cases, but it is a stress test for both sides. If plaintiffs get a strong liability finding or meaningful damages, it forces the defense to price the risk across the docket. If the defense wins by narrowing claims or exploiting weak facts, it will try to use that result to push down settlement values.
    What plaintiffs want before trial A clear ruling that lets key defect and warning theories reach a jury, plus an evidence record showing what Covidien knew about performance problems and how it marketed these meshes. Trial dates create urgency. Without them, defendants can litigate “forever” at the pretrial stage.
    Key takeaway for readers The strongest Covidien cases usually involve revision surgery with documented mesh involvement. If you have operative reports showing adhesions, obstruction, recurrence, infection, or difficult removal, you are in a different category than someone with pain complaints alone.  Our lawyers do not take a case without a revision.
    COVIDIEN UPDATE:  The MDL is moving toward a trial.  Finally.  Plaintiffs get a chance to put the device story and the injury story in front of jurors. It has taken a long time to get there

    January 30, 2026 – New Study

    new study examined 31 studies on robotic hiatal hernia (HH) repair and compared outcomes with traditional laparoscopic techniques. The analysis found that robotic surgery is generally safe and feasible, with complication and recurrence rates similar to those of conventional surgery. Benefits cited include improved 3D visualization, better dexterity, and potential advantages in complex cases, especially for overweight or obese patients. Some studies noted shorter hospital stays and reduced blood loss, though operative times were sometimes longer and costs consistently higher.

    The review also discussed mesh use. While mesh can lower recurrence rates, it carries risks such as esophageal erosion. Some robotic techniques avoid mesh altogether, using precise suture closure with promising early results. Surgeons’ experience significantly affects outcomes, with learning curves ranging from 7–15 cases for efficient, safe procedures. Overall, the evidence suggests robotic HH repair is a viable alternative to laparoscopy, but long-term randomized studies are lacking.

    How could this study be used in the mesh litigation?  The findings suggest that mesh-free approaches exist and are safe, making a warning about the risks all that more important.

    Relevance to Hernia Mesh Litigation

    This review could support plaintiffs’ arguments that surgical outcomes depend heavily on technique and operator experience, not just on the product. Evidence of complications from mesh, even in robotic cases, reinforces claims about risk, precision, and informed consent. Demonstrating that alternative, mesh-free approaches exist and are safe may bolster arguments that patients were exposed to unnecessary risk. Moreover, the documented variability in complication rates and outcomes could be used to question manufacturer claims of consistent safety, highlighting the importance of proper surgical technique alongside device design.

    More Pre- 2026 Hernia Mesh Lawsuit Updates 👈

    September 1, 2025 – More Lawsuits Filed Before Possible Settlement

    There is an increasing number of Covidien hernia mesh lawsuits being filed in anticipation of a possible settlement.

    In a new lawsuit filed on Friday in the District of Massachusetts as part of the Covidien Hernia Mesh MDL, a New Mexico resident alleges that he suffered serious complications following the implantation of a defective hernia mesh product manufactured by Covidien LP and Sofradim Production SAS. The plaintiff claims he was implanted with the Parietex Optimized Composite Mesh on or about August 2, 2021, in New Mexico, and has since required corrective surgery due to complications from the device.

    The lawsuit incorporates claims from the MDL’s Master Complaint, asserting causes of action for strict product liability (defective design, failure to warn, and manufacturing defect), negligence, gross negligence, and violations of both New Mexico and Massachusetts consumer protection laws. It also alleges breach of warranty, negligent and intentional infliction of emotional distress, fraudulent misrepresentation and concealment, and seeks punitive damages.

    August 21, 2025 – Settlement

    Judge Patti Saris granted Covidien and Medtronic an additional four months to participate in mediation, extending the settlement deadline to January 14, 2026. That is a win for the defense, which has every incentive to stall, but it does nothing for the thousands of patients who have been waiting years for justice. Plaintiffs want a trial, not another extension, and thankfully, the judge kept the February 2026 bellwether date locked in. That date is the critical pressure point.

    Because, until a jury rules, Covidien can continue to prolong this. A February verdict is the moment of truth, the scoreboard that will drive real settlement dollars. Plaintiffs know it, defendants know it, and the court knows it. This extension just stretches the pregame warm-up. The real fight begins when those bellwether trials start, and that is where plaintiffs finally get what they want… a jury weighing the evidence.

    August 4, 2025 – Bard Hernia Mesh MDL Case Count and Settlement Context

    As of August 1, 2025, 24,029 active cases are pending in MDL 2846, consolidated in the Southern District of Ohio before Judge Edmund Sargus.  This tells us two things: (1) new cases are still being filed post-settlement, and (2) the process of getting settlement checks is taking longer than victims would have hoped. 

    July 29, 2025 – Strattice Hernia Mesh Lawsuits

    The Strattice hernia mesh litigation is quietly evolving into a significant but often overlooked mass tort. While Bard and Covidien dominate the conversation, largely because of the enormous number of cases filed against them, Strattice has remained under the radar.

    The Bard MDL alone has drawn so much judicial and media attention that it has effectively crowded out other claims involving similarly dangerous mesh products. But the Strattice litigation deserves attention in its own right, particularly because it raises serious questions about the safety of biologic mesh.

    Strattice is made from porcine tissue, preserved through chemical cross-linking. It was marketed as a safer alternative to synthetic mesh for hernia repair, especially in complex or high-risk patients. Plaintiffs now argue that it causes many of the same problems as its synthetic counterparts, including chronic infections, foreign body responses, and tissue degradation. The FDA has received over 450 adverse event reports tied to Strattice, including hundreds of injuries and multiple deaths. That is not a signal to ignore. It is a warning that this device, biologic or not, carries risks that may have been underplayed.

    While many of the Strattice cases have been filed in New Jersey state court and coordinated through a multicounty litigation, a separate and growing group is being litigated in federal court in the District of New Jersey. That federal proceeding is now under the management of U.S. Magistrate Judge Leda Wettre, with the first bellwether trial scheduled for February 2026. The court has issued a detailed schedule for expert disclosures, dispositive motions, and Daubert hearings. The seventh amended case management order outlines deadlines that stretch into late October, signaling that the parties are entering the heart of pretrial litigation.

    Although the number of Strattice cases does not yet rival the Bard MDL, the claims are built on the same core theories of liability: design defects, failure to warn, and inadequate testing. What sets Strattice apart is the focus on biologic mesh, a product category that has been marketed as more compatible with human tissue. The litigation challenges that narrative and puts the safety of cross-linked biologics under the microscope.

    This is not just a smaller version of Bard. It is a distinct battleground, and for plaintiffs’ lawyers already working in the mesh space, it offers another path forward. The Strattice litigation is likely to shape how courts and juries view biologic mesh, and it may open the door to broader scrutiny of devices once assumed safer simply because they were not synthetic.

    July 16, 2025 – New Covidien Lawsuit

    A New Mexico woman has sued Covidien and Sofradim Production SAS, alleging injuries from the implantation of a Symbotex Composite Mesh hernia device.

    Filed as part of the hernia mesh multidistrict litigation in the District of Massachusetts, the suit contends that the plaintiff required surgical intervention following the 2016 implantation procedure.

    The plaintiff asserts multiple claims, including defective design, failure to warn, manufacturing defect, and various negligence-based counts. She also invokes New Mexico and Massachusetts consumer protection laws and seeks punitive damages. The case underscores ongoing concerns in the hernia mesh litigation involving allegations of inadequate testing and misrepresentations about the safety and efficacy of the mesh products.

    July 10, 2025 – Bard Mesh Lawsuits Moving Forward

    Our lawyers are still seeing a steady flow of new Bard hernia mesh lawsuits. Not a ton of lawyers are looking at new cases but we are.

    Many of these cases are coming from patients who only recently connected their chronic pain or surgical complications to their earlier mesh implant. That delay between implantation and diagnosis is common and expected.

    Hernia mesh complications often emerge slowly over time as the material breaks down, adheres to tissue, migrates, or causes infection or inflammation. A person might live for months or even years with unexplained pain, digestive issues, or hernia recurrence before a doctor pinpoints the underlying issue as mesh failure.  So these cases will go on for a while.

    The process for settling new cases is still likely pretty far away. That is the reality. The next major procedural step will not begin until January 2027, when the court launches the Inventory Settlement Process (ISP). This will mark the formal start of active settlement negotiations–but that is still more than two years away. In the meantime, plaintiffs must wait, and their cases remain in procedural limbo.

    The ISP is designed to last until all claims are addressed. However, for those whose claims are not resolved by June 2029, there will be an option to opt out of the process and resume individual litigation. That means some victims may still be without a resolution four-and-a-half years from now.

    Bard might decide it wants to get rid of these cases hanging over its head and offer a fair settlement. This is possible. But honestly, we think it is unlikely.

    June 2, 2025 – Case Count Updates

    The two major hernia mesh multidistrict litigations—Bard and Covidien—continue to move forward, albeit on different tracks.

    • Bard Hernia Mesh MDL (MDL No. 2846 –  S.D. Ohio):  As of June 1, the Bard Hernia Mesh MDL has 25,015 active cases, up from 24,074 at the start of May. That is a net increase of 941 cases in just one month.

    Although a major settlement resolved many claims last year, the litigation remains open and active. New lawsuits continue to be filed, while some older cases are being dismissed—either through resolution or procedural steps. The increase shows that despite earlier deals, Bard is still facing ongoing legal exposure as additional plaintiffs step forward.

    • Covidien Hernia Mesh MDL (MDL No. 3029 –  D. Mass.)

    The Covidien MDL experienced slower movement last month, adding six new active cases to bring the total to 2,004, up from 1,998. This litigation is still in an earlier phase compared to Bard, with discovery and case development continuing. Plaintiffs’ Covidien hernia mesh lawyers are excited about the upcoming bellwether trial.  Normally, we say we think the defendants will try to settle before the significant bellwether. But this case might get tried. Because I don’t think Covidien settlement amounts will be as low as they were for Bard.

    May 21, 2025 – New Hernia Mesh Lawsuit

    A federal hernia mesh lawsuit filed by a Mississippi woman has been selected as the second bellwether case in the Covidien hernia mesh multidistrict litigation (MDL No. 3029). Her trial is scheduled to begin on July 13, 2026, in the U.S. District Court for the District of Massachusetts. Again, the first bellwether is set for February 17, 2026, involving an Alabama plaintiff who alleges a defect in her Parietex Optimized Composite Mesh.

    The second bellwether trial involves allegations that a Symbotex hernia mesh device implanted in January 2017 during ventral hernia repair caused severe complications, including adhesions, chronic inflammation, bowel problems, infections, and the need for corrective surgery. The lawsuit alleges that the collagen coating on the mesh prematurely resorbed, thereby defeating its intended purpose of preventing adhesion.

    The problem in getting these cases settled before that trial is the Bard settlement.  Covidien will not get the exact numbers that Bard got. If they are waiting for that, those trials will go forward.

    May 8, 2025 – New Hernia Mesh Lawsuit

    Settlement or not, new lawsuits continue to flow. In one new suit, a Virginia resident has sued Bard, alleging serious injuries stemming from the implantation of a hernia mesh device. The plaintiff, a resident of Kenbridge, Virginia, underwent hernia repair surgeries at VCU Medical Center in February 2022 and again in March 2023. During the second surgery, Bard’s 3D Max Mesh product was implanted.

    The lawsuit claims that the mesh caused severe complications, including a recurrent incisional hernia, extensive adhesions requiring surgical removal of the mesh, and a left orchiectomy. The plaintiff asserts that Bard, both individually and as the parent company of Davol, Inc., is liable for designing, manufacturing, marketing, and distributing a defective medical device. The complaint emphasizes Bard’s failure to meet applicable safety standards, alleging inadequate warnings and improper labeling.

    The plaintiff contends that Bard derived substantial revenue from the interstate sale of hernia mesh devices and exercised direct control over product safety and adverse event reporting. Jurisdiction is asserted in New Jersey based on Bard’s corporate presence and business operations within the state.

    April 11, 2025 – Bellwether Trial Set in Covidien

    se because the polyester used in Covidien’s products is even more problematic than the materials used by Bard.

    Covidien Plaintiffs claim that polyester incites inflammation and a heightened foreign body response. It is described as being more brittle and significantly more susceptible to fatigue fracture, breakage, fragmentation, and other mechanical failures. Bard’s hernia mesh typically used polypropylene, which, with all of its flaws, does not have the same level of brittleness or susceptibility to mechanical failures as alleged with polyester.

    As of May 1, there were 1,081 cases in the Covidien MDL-3029.

    When will the Covidien hernia mesh case settle?  Let’s just say that is projected to be after the Bard settlement, although there is hope for a domino effect.

    March 19, 2024 – Settlement Is Focus

    All the energy in the hernia mesh litigation – even for non-Bard cases – is centered around settlement negotiations set to begin on Monday.  Too many victims have waited far too long.  Are the parties far apart at this point?  No.  But even small differences are many millions of dollars.

    After all this time, the plaintiffs want to get as much as possible.  Bard wants to pay as little as possible, and there are no trial dates to put real pressure on them to move off its position.  Still, there is a sense Bard wants to move on from this. It has other litigation – the BardPowerPort litigation is getting in full swing – to manage.  If these cases get remanded, Bard’s legal costs will escalate quickly.  Hopefully, that realization forces Bard to offer reasonable settlement amounts to resolve these lawsuits.

    March 16, 2024 – Settlement Circle Is Small

    Judge Sargus issued an order that establishes the mediation plan and schedule aimed at facilitating settlement in the Bard hernia mesh MDL.

    According to the order, an in-person mediation session is slated for March 25 and March 26, 2024. The parties involved will convene under the guidance of Court-Appointed Mediator John Jackson, with further meetings subject to the mediator’s discretion.

    However, if the parties fail to reach a mutually acceptable resolution or extend the deadline for discussions, they must notify the court of an impasse by May 24, 2024. In the event of an impasse, the parties are directed to collaborate on a joint proposal outlining a plan for advancing the litigation, including suggestions for remand. This proposal, or individual submissions if no consensus is reached, must be submitted by June 24, 2024. The court may then set a schedule for subsequent briefing and/or argument on the proposals.

    These settlement negotiations that impact thousands of plaintiffs do not require a big conference room like you might think.  The group is small.  The plaintiffs will send just three lawyers on their negotiation committee.

    March 1, 2024 – Covidien MDL

    Judge Saris, the Covidien MDL judge, has ordered the company to release a significant number of complaint files in the pretrial discovery process. These documents detail the issues faced by individuals following the use of hernia repair products distributed in the last decade.

    Covidien was instructed to submit an extensive collection of hernia mesh complaint files without redactions to speed up the production process. As it should, this order bars plaintiffs from using any personal data from the complaint files unless they demonstrate a valid reason and obtain court or defendant approval.

    It has been slow but this litigation is starting to move forward. Key deadlines have been set, including October 14, 2024, for submitting dispositive or Daubert motions, and November 22, 2024, for responses to these motions.  So we are looking at a bellwether trial in 2025.

    January 4, 2024 – Plaintiffs’ Want to Push Ball Forward Faster

    What would put more pressure on Bard to make a reasonable settlement offer in the hernia mesh lawsuits in 2024?  More trials.  Plaintiffs keep winning but the spacing of these wins zaps some of the momentum.

    The plaintiff’s hernia mesh lawyers have been trying to change this, asking for a new Case Management Order to oversee the future handling of cases and potential remand to state court where we can start trying these cases in multiple jurisdictions.  Plaintiffs’ attorneys argue that it’s time for an order that sets out a process for remand to ensure plaintiffs, many of whom have been waiting for nearly six years, will get their day in court or reach a fair resolution of their claims.

    Their proposed order doesn’t suggest dumping all cases into district courts at once but rather working up cases in large groups at intervals. Once case-specific discovery is done, cases will be remanded back to the original district courts. The first group includes 1,500 cases, about 7.5% of the total filed cases.

    The attorneys argue that continuing at the current pace of 1 to 2 trials per year would be impractical, taking thousands of years to try every case. They propose a measured approach to remand, beginning the process now, and organizing it in a logical and efficient manner. This includes selecting cases based on severity of injury, length of time filed, and involvement in bellwether trials. They also suggest multi-plaintiff trials to allocate costs efficiently and avoid duplicate testimony.

    Here is where we are after four trials.

    CASE DATE RESULT VENUE
    Stinson Oct 2023 $500,000 MDL
    Trevino Aug 2022 $4.8 million Rhode Island
    Milanesi April 2022 $250,000 MDL
    Johns July 2021 DEFENSE MDL

    Hopefully, if Bard is not going to come to its senses, we can have four trials a month instead of four trials over two-and-a-half years.

    December 5, 2023 – Ethicon Settlement in Georgia

    Johnson & Johnson and its subsidiary Ethicon, have reached a settlement in a Georgia multidistrict litigation involving 224 lawsuits.

    The settlement agreement was formalized with a joint motion for dismissal of the claims, which was filed by both parties and subsequently granted by U.S. District Judge Richard W. Story. Ethicon Inc. issued a statement with the usual blah blah blah about its commitment to patient safety and reminding us all that the settlement is not an admission of liability or wrongdoing. They stated that the decision to settle was made to avoid a prolonged legal process.

    This settlement follows a previous agreement approximately six months earlier, where the companies had settled with 161 plaintiffs in the same MDL

    November 9, 2023 – $500,000 Verdict

    The jury came back in Stinson with a $500,000 verdict.  It is not $4.8 million like the last one, but this is a big win.  Plaintiffs are winning these cases.

    Here is the verdict sheet from the jury..

    July 1, 2023 – Post-Trial Conversations with Jurors

    In the first bellwether trial, the Johns case that is discussed below in the older updates, resulted in a defense verdict.  One lesson the plaintiffs got from that verdict is that Mr. Johns’ failure to seek additional medical treatment did not help his cause.

    A lawyer in the MDL leadership said this to someone who put it on their website.  Bard, being petty, thought that the attorney must have talked to a juror.  Ohio has a local rule that you cannot talk to jurors after the trial without the court’s permission (which is a little bit of an unusual rule).

    So, already fearful that the next two cases going to trial are not “representative” because the victims have severe injuries, they filed a motion complaining about his breach of ethics and saying the cases that went to trial after Johns were not representative of the other cases in the MDL.  But the plaintiffs’ attorneys were able to explain that the ‘feedback’ mentioned was based on a jury question during deliberations and the Court’s comments in a meeting with the PSC.

    This satisfied Judge Argus. So Bard just wasted everyone’s time chasing windmills instead of working on offering a reasonable settlement amount to resolve the 20,000 lawsuits against it.

    ut mediation efforts are advancing.

    📈 Case Numbers

    • Bard: 27,000+ pending cases (post-settlement)
    • Covidien: 2,396 pending federal cases
    • Atrium: 436 pending
    • Ethicon: Mostly settled (16 pending)

    🚩 Legal Issues & Allegations

    • Design defects (polypropylene and polyester mesh degradation, improper collagen resorption)
    • Failure to warn about risks (adhesions, chronic pain, infections, recurrence)
    • Marketing misrepresentations and post-market concealment of adverse outcomes

    📞 Need Legal Help?

    If you or a loved one suffered complications after hernia mesh surgery, contact our legal team at 800-553-5053 for a free consultation.

    Summary of the Hernia Mesh Lawsuits

    A hernia mesh is a small piece of surgical mesh or screen used to reinforce and strengthen tissue walls in hernia surgeries. The hernia mesh products at issue in the lawsuits suffered from a host of similar defects in their design which caused them to fail.

    Some of the mesh products were made out of materials that were not “biologically inert,” which caused the patient’s immune system to reject the mesh as a foreign object. Other mesh products had a design flaw that caused them to attach and fuse abnormally into the adjacent tissue.

    The defects in these hernia mesh implants caused them to fail after being implanted. The results were severe post-surgical complications, which eventually required the patients to undergo corrective surgery to remove the defective mesh. Many patients were left with permanent injuries.

    As these hernia mesh injuries started accumulating, a steady stream of product liability lawsuits were filed in response. Within a year, the number of hernia mesh lawsuits in federal courts around the country was enough to trigger the Judicial Panel on Multidistrict Litigation to create three new class action MDLs for consolidated handling of the cases:

    1. The Bard Hernia Mesh MDL (In re: Davol, Inc./C.R. Bard, Inc., Polypropylene Hernia Mesh Products Liability Lit. – MDL-2846)
    2. The Ethicon Hernia Mesh MDL (In re: Ethicon Physiomesh Flexible Composite Hernia Mesh Products Liability Lit. – MDL-2782) (which has recently settled, but new cases will continue to be filed)
    3. Atrium C-Qur Hernia Mesh MDL (In re: Atrium Medical Corp. C-Qur Mesh Products Liability Litigation – MDL-2753)

    The ProLite, Strattice, and ProLoop (manufactured by Atrium Medical Corp.) are the latest polypropylene hernia mesh products to be the subject of a growing wave of product liability lawsuits.

    The lawsuits allege that the polypropylene material these products are made from is defective because it is not biologically inert and degrades inside the body, leading to infections and chronic pain. Atrium is accused of ignoring scientific studies showing the various problems with polypropylene mesh implants.

    Lawyers for some of the plaintiffs in the ProLite hernia mesh lawsuits filed a motion asking the Judicial Panel on Multidistrict Litigation to consolidate all pending ProLite and ProLoop lawsuits into a new MDL.  But this effort was rejected, and these cases will proceed as individual claims.

    What Is the Nutshell of the Allegations in the Bard Hernia Mesh Class Action?

    If you are trying to understand the Bard hernia mesh lawsuits, the core allegation is pretty straightforward. Plaintiffs say Bard sold hernia mesh products that were supposed to help repair their bodies, but instead caused serious and sometimes life-changing complications. Bard, a subsidiary of Becton Dickinson, manufactured the hernia mesh devices at the center of these claims.

    We argue that these products were defectively designed and improperly manufactured. We also say that the mesh did not perform the way a safe medical device should. Instead of acting like a sturdy patch on a torn sail, plaintiffs claim the mesh sometimes became the very thing that created more damage. The alleged complications include chronic pain, infections, mesh migration, mesh shrinkage, organ perforation, and hernia recurrence. For many patients, that meant more surgery, more pain, and a longer road than they ever expected.

    Allegation That Bard Knew of the Risk

    A major allegation in the Bard hernia mesh litigation is that Bard knew or should have known about the risks associated with its mesh products and failed to give doctors and patients fair warnings. This allegation really drives these cases. A complication is one thing. But what if the manufacturer understood the danger and still did not clearly tell the people who needed that information most?

    So our lawyers contend that Bard did not adequately disclose the risk of serious mesh-related complications or provide proper instructions for safe use of the devices. The argument is that surgeons and patients were left without a full picture of the risks before these products were implanted.

    Compensation Sought

    The plaintiffs are seeking compensation for the harm they say Bard’s hernia mesh products caused. That includes damages for physical injuries, chronic pain, additional surgeries, emotional distress, medical bills, lost wages, and the cost of future care.

    These lawsuits are not just about the mesh failing. They are about the human cost that follows when a medical device allegedly creates more problems than it solves. If you had a hernia repair and later needed revision surgery, suffered ongoing pain, or developed serious complications, you can see why plaintiffs are pushing to hold Bard accountable. The claim is that patients trusted the product to help fix one problem, but for too many people, it allegedly opened the door to another.

    Settlements in Prior Surgical Mesh Cases

    Estimating the potential settlement amounts of product liability claims in a mass tort is hardly an exact science. There are too many variables and unknowns that can have a drastic impact on settlement compensation.

    In the hernia mesh litigation, in addition to the bellwether trials, we do have some prior verdicts in earlier hernia mesh or surgical mesh defect lawsuits. These results give us some basis to come up with a reasonable value estimate for the present cases. The prior mesh litigation involved C.R. Bard and its Kugel Hernia Mesh product.

    What Is the Expected Settlement Amount for the Average Hernia Mesh Lawsuit?

    Based on the awards in the Kugel hernia mesh litigation and results in similar medical device cases, our lawyers believe that claims in the current hernia mesh litigation will end up with a settlement ranges between $10,000 and $1,000,000.

    The reason this range is so broad is that the value of each individual claim will vary significantly based on the level of injury involved. What do we think the average hernia mesh settlement be?  Our guess – and we are getting closer to the end of this thing is – the average hernia mesh payout will be between $70,000 and $80,000. 

    If you think your case is more serious than the average and deserves a higher settlement, you may choose to opt out of any global settlement and keep going forward with your claim.

    Prior Mesh Settlement Amounts

    The Kugel was an earlier type of hernia mesh. Unfortunately, it had a serious design flaw, which caused a plastic ring on the mesh to break off inside the patient after being implanted. This caused painful bowel obstruction and required corrective surgery – very similar to the injuries involved in the current hernia mesh cases.

    After a $1.5 million verdict in the first Kugel bellwether case, Bard agreed to a $184 million global settlement, which amounted to $70,000 per claim. Not all claimants received the same amount, however, with some getting more and some less than $70,000 per person.

    The settlement in the Kugel hernia mesh litigation resulted in a very similar value range for individual cases. The total Kugel hernia mesh lawsuit settlement payment of $184,000,000 resolved just over 2,000 individual claims, which equals about $70k per claim.

    But each plaintiff in the Kugel litigation did not simply get a $70,00 check. Instead, the plaintiffs were grouped into settlement tiers with a points system based on the level of injury they suffered. Plaintiffs in Tier 1 had the most severe injuries and reportedly received around $900,000. Tier 2 plaintiffs reportedly received less than half of this amount, and the bottom-tier plaintiffs got much less than the $70k per claim average.

    Vaginal Mesh Also Gives Us Settlement Amount Clues

    We saw similar mesh lawsuit settlement numbers in another mass tort case involving Endo International’s vaginal mesh implants. In that litigation (which had many similarities to the hernia mess litigation), Endo paid $900 million to settle about 20,000 individual claims. This worked out to an average individual settlement amount of $45,000 per claim. But the settlement proceeds were distributed based on a tiered settlement system. The cases in the lowest settlement tier received very little, while plaintiffs in the top tier received over $500,000.

    Of course, some plaintiffs opted out of the Kugel hernia mesh settlements.  Bard veterans will remember a jury awarded a plaintiff $3.6 million in a mesh lawsuit in 2016. In 2018, another jury awarded a plaintiff $18.5 million in a mesh lawsuit (Boston Scientific was the defendant).  So Bard understands that juries will award large verdicts in mesh cases where the injuries are severe.

    Do I Qualify for a Hernia Mesh Lawsuit?

    You may qualify for a hernia mesh lawsuit if you underwent hernia repair surgery in which a mesh was used and you subsequently suffered serious post-surgery complications such as adhesion or infection that were potentially related to defects in the hernia mesh.

    (In this sense, “qualify” is defined as our hernia mesh lawyers being willing to take your case.)

    Contact Us About Your Hernia Mesh Case

    It is not too late to file your hernia mesh lawsuit. If you were injured by a defective hernia mesh implant, call our hernia mesh lawyers today at 800-553-5053.