Hernia Mesh (Davol/C.R. Bard) Lawsuit in Michigan

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Statute of limitations — Michigan

Michigan Compiled Laws § 600.5805(2) provides a 3-year limitations period for product liability personal injury claims. The discovery rule applies to latent injury cases. Michigan's statute of repose (MCL § 600.5839) bars claims more than 10 years after the product was first sold to the plaintiff. Michigan uses a modified comparative fault system — recovery is barred if plaintiff's fault is 51% or more.

3 years from discovery; 10-year statute of repose

Filing venue

Where to File in Michigan

Michigan hernia mesh claimants are routed by product to: Davol/CR Bard MDL 2846 (S.D. Ohio, Judge Sargus); Covidien Parietex MDL 2511 (S.D. Ohio, Judge Sargus); Atrium C-QUR MDL 2753 (D.N.H.); and Ethicon/J&J Physiomesh and Prolene cases to the Atlantic County NJ Superior Court mass tort before Judge Porto. Michigan's Eastern District (Detroit) is the common originating federal court before JPML conditional transfer.

Michigan applies a three-year statute of limitations for products liability under MCL § 600.5805(13), with the discovery rule tolling the period until the plaintiff discovered or should have discovered the injury and its cause. Michigan also has a product liability statute of repose of ten years from the date of delivery, but the discovery rule governs accrual within that window. Mesh complications arising years after implantation — erosion, bowel obstruction, seroma — are squarely within Michigan's discovery-rule framework.

Michigan's major hernia mesh implant centers include Henry Ford Health, Michigan Medicine (University of Michigan), Beaumont Health, and Spectrum Health in Grand Rapids. The Detroit metro area and Flint-Lansing corridor generate significant surgical volume. Bard Davol's PerFix Plug, Ventralex, and Composix L/P products are heavily represented in Michigan defendant product distribution. Michigan's large manufacturing and industrial workforce has historically elevated hernia incidence, driving above-average mesh implant rates.

Michigan Ethicon plaintiffs should file in Atlantic County, NJ Superior Court under the mass tort designation rather than seeking a federal transfer, as there is no federal MDL for Ethicon hernia mesh. Judge Porto's Atlantic County docket accepts Michigan plaintiffs, and Michigan firms with NJ co-counsel relationships can efficiently file direct actions in that forum. The geographic proximity to S.D. Ohio also makes MDL 2846 and 2511 convenient for Bard and Covidien Michigan plaintiffs.

Michigan data

Exposure in Michigan

Michigan's 3-year SOL for product liability is among the more generous deadlines, providing a wider window for mesh complication claimants

3-year SOL

Source: MCL § 600.5805

Michigan's large manufacturing workforce experiences elevated hernia rates from heavy lifting, increasing mesh complication caseloads among working-age claimants

Auto industry workforce

Source: Michigan Bureau of Labor Statistics

Estimated annual hernia repair surgeries in Michigan

~25,000

Source: Michigan Health and Hospital Association

Medical resources

Clinics & Specialists in Michigan

Michigan Medicine (University of Michigan) — Comprehensive Hernia Center

Henry Ford Hospital — General Surgery Department

FAQ

Frequently Asked Questions

12 QUESTIONS

Hernia mesh litigation is a mass tort action against manufacturers of defective synthetic mesh implants used in hernia repair surgery. The primary defendants are Davol Inc. and C.R. Bard (now part of Becton Dickinson), Ethicon (a subsidiary of Johnson and Johnson), Atrium Medical, and Covidien (now part of Medtronic). These companies manufactured polypropylene and composite mesh devices that have been associated with serious complications including mesh migration, adhesion, infection, chronic pain, and bowel obstruction. Thousands of patients have filed claims in MDL 2846 in the Southern District of Ohio and in state court coordinations.

The most litigated hernia mesh products include Davol/Bard 3DMax, Ventralex ST, Composix E/X, Composix Kugel (recalled 2005-2007), and Marlex; Ethicon Physiomesh Flexible Composite (voluntarily withdrawn globally in 2016), Proceed, and Prolene Soft; Atrium C-QUR; and Covidien Parietex and Symbotex. If you are unsure which mesh was used in your surgery, the operative report from your hernia surgery will identify the product by name, manufacturer, and lot number. Request this record from your surgeon's office or the hospital's medical records department.

Common signs of hernia mesh failure include: persistent or worsening pain at the original surgical site, a bulge or lump near the incision suggesting hernia recurrence, redness, swelling, or drainage from the wound, fever and chills suggesting infection, nausea and bowel problems that may indicate adhesions, or groin pain radiating into the thigh or genitals. Many patients experience symptoms for months or years before receiving a diagnosis connecting their pain to the mesh. If you have any of these symptoms after hernia repair surgery, see your doctor and request imaging (CT scan or MRI) to evaluate the mesh. Then contact an attorney to evaluate your legal options.

Qualifying complications include mesh migration (the mesh has moved from its original position), surgical site infection that required prolonged antibiotics, hospitalization, or surgery, mesh adhesion to the bowel or other organs, hernia recurrence (the hernia came back despite the mesh), chronic pain syndrome or inguinodynia lasting more than 3 months, bowel obstruction or fistula formation, and any complication requiring revision surgery or mesh removal. The strongest cases involve documented complications in medical records and at least one revision or explantation surgery. However, patients who have not yet had revision surgery but have documented complications may also have valid claims.

Hernia mesh cases are consolidated in multidistrict litigations (MDLs), not class actions. The distinction matters: in a class action, one settlement covers all plaintiffs. In an MDL, each plaintiff's case retains its individual identity and is ultimately resolved based on that person's specific injuries. The primary hernia mesh MDL is MDL 2846 in the Southern District of Ohio before Judge Edmund Sargus, which consolidates Davol/C.R. Bard claims. Ethicon mesh cases are in MDL 2753 in New Jersey federal court. New Jersey state court Ethicon cases are in MCL 616. Your attorney will file in the appropriate court based on which mesh product you received.

Hernia mesh claims in MDL 2846 and related litigations typically take 3 to 6 years from filing to resolution due to the complexity of mass tort proceedings. However, this estimate depends heavily on where the litigation stands when you file and whether a global settlement is negotiated. Some cases settle individually before any global resolution. During this time, plaintiffs are not required to appear in court — attorneys handle the MDL proceedings while plaintiffs complete their Plaintiff Fact Sheet and participate in depositions if selected. Staying in active treatment and maintaining complete medical records throughout the litigation period strengthens your claim value.

Revision surgery is not an absolute requirement to file a claim, but it significantly strengthens the case and typically places it in a higher settlement tier. Patients who have had mesh-related complications documented in medical records — even without surgery — may still have viable claims, particularly if they suffer from chronic pain, infection, or other documented consequences. However, MDL case administrators and defendants generally assign higher settlement values to cases involving documented surgical intervention because the complication severity is objectively verified. If your physician has recommended revision surgery, that recommendation itself is important supporting documentation even if the surgery has not yet occurred.

Hernia mesh plaintiffs can recover: past medical expenses related to treating mesh complications and revision surgery; future medical costs for anticipated ongoing treatment; lost wages during recovery periods; diminished earning capacity if complications caused permanent disability; pain and suffering, including chronic pain syndrome; emotional distress and loss of enjoyment of life; and loss of consortium (impact on the marital relationship). In cases where the manufacturer's conduct was particularly egregious — such as documented concealment of known risks — punitive damages may be awarded at trial. Mass tort settlements typically compensate economic damages plus a pain and suffering component scaled to injury severity.

Most states impose a 2- to 3-year statute of limitations for product liability claims, but hernia mesh cases benefit from the discovery rule in most jurisdictions. Under the discovery rule, the clock starts when you knew or reasonably should have known that your injury was caused by a defective mesh product — not on the date of your original surgery. This means patients implanted years ago may still have timely claims if their complications are recent. However, some states have statutes of repose that impose an absolute outside limit. Do not assume your case is time-barred without consulting an attorney — the analysis is state-specific and fact-dependent.

You need records from multiple sources: (1) The hospital where your original hernia surgery was performed — request the operative report and any implant documentation (the implant sticker identifies the exact mesh product). (2) Your surgeon's office — for pre-operative notes and post-operative follow-up records. (3) Any hospital or facility where revision or explantation surgery was performed — request the operative report and pathology reports. (4) Any imaging center — for CT scans, MRIs, or ultrasound reports. You have a legal right to all your medical records.

Hernia mesh litigation typically requires several categories of expert witnesses: (1) A general surgeon or hernia specialist to opine that the mesh product caused the plaintiff's complications. (2) A biomaterials expert to explain why polypropylene mesh degrades, shrinks, or fails — and what the manufacturer knew about these properties. (3) A regulatory expert to address whether the FDA's 510(k) clearance process adequately vetted the device and whether the manufacturer provided accurate risk information. (4) An economist to calculate lost wages and future earning capacity if applicable. In MDL 2846, plaintiff leadership has developed a shared pool of general experts who testify in bellwether trials and whose opinions support individual case settlements.

As of 2026, there is no announced global settlement for MDL 2846 (Davol/C.R. Bard). Individual cases have resolved through negotiated settlements, particularly those selected for bellwether trials or cases in advanced stages of discovery. Ethicon Physiomesh cases have seen individual settlement activity. The absence of a global settlement means claimants are in an active litigation posture — which makes filing and completing the required Plaintiff Fact Sheet now critically important. When a global settlement is eventually negotiated, only plaintiffs with timely-filed, complete cases will be eligible to participate. Claimants who waited and missed the statute of limitations or failed to register in the MDL will be excluded.

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Where to File in Michigan

Exposure in Michigan

Clinics & Specialists in Michigan

Michigan Medicine (University of Michigan) — Comprehensive Hernia Center

Henry Ford Hospital — General Surgery Department

Frequently Asked Questions

What is hernia mesh litigation and which companies are being sued?

Which hernia mesh brands are involved in lawsuits?

How do I know if my hernia mesh has failed?

What complications qualify for a hernia mesh lawsuit?

Is there a class action or MDL for hernia mesh?

How long does a hernia mesh claim take to resolve?

Do I need to have had revision surgery to file a hernia mesh claim?

What damages can I recover in a hernia mesh lawsuit?

What is the statute of limitations for hernia mesh claims?

How do I get my hernia mesh medical records?

What expert witnesses are needed in a hernia mesh case?

Are there hernia mesh settlements available?