Hernia Mesh Lawsuit Settlement Calculator
Three active MDLs for defective polypropylene mesh — bowel obstruction, fistulas, chronic pain, revision surgery. 25,909 cases pending as of the JPML's August 2026 report. First bellwether $255M (reduced to $80M).
⚖ 4 Active MDLs: Bard 2846 (S.D. Ohio) settlement framework; Ethicon 2782 nearly resolved; Atrium 2753 ~500 cases; Covidien first bellwether July 2026.
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$105,000 — $195,000
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Hernia Mesh Litigation — 4 Active MDLs
Defective polypropylene hernia mesh products contracted, degraded, migrated, or caused adhesions post-implantation — leading to bowel obstruction, fistulas, chronic pain, and required revision surgery. 25,909 cases were pending across three active MDLs as of the JPML's 3 August 2026 report — 23,321 against Bard/Davol (MDL 2846), 2,449 against Covidien (MDL 3029) and 139 in the Atrium C-Qur litigation (MDL 2753). A fourth, Ethicon Physiomesh (MDL 2782), has closed out at zero pending cases after 4,054 filings.
MDL 2846 Bard Hernia (S.D. Ohio): Becton Dickinson entered a settlement agreement in the fourth quarter of its fiscal year 2024 resolving "the vast majority of its existing hernia litigation," payable over a multi-year period — but the terms are not public and the court's own published order list for MDL 2846 contains no settlement allocation order. BD reported approximately 7,090 hernia claims pending at June 30, 2026, up from 6,905 at September 30, 2025, and stated "there are no trials currently scheduled" (Form 10-Q filed August 6, 2026). MDL 2782 Ethicon Physiomesh (N.D. Ga.): nearly resolved — only ~16 cases remaining after mass settlement. MDL 2753 Atrium C-Qur (D.N.H.): ~500 pending. MDL 3029 Covidien (D. Mass.): first bellwether (Patterson v. Covidien) postponed to July 2026.
Bard bellwether: $255M punitive verdict (reduced on appeal to $80M). Individual Bard verdicts routinely $1M-$5M. Ethicon settled after plaintiff verdicts. Covidien outcome critical — no verdicts yet. Typical settlement values: low (hernia recurrence, minor revision) $20K-$60K; moderate (significant revision, chronic pain) $60K-$100K (median); severe (bowel obstruction, multiple surgeries) $100K-$500K+.
Hernia Mesh Lawsuit FAQs
Which hernia mesh brands are covered by active litigation?
Bard (3DMax, Perfix, Ventralex), Ethicon (Physiomesh), Atrium (C-Qur), Covidien (Symbotex, Parietex). Each has its own MDL with specific eligibility. If you had mesh from an unbranded or other manufacturer, consult an attorney — some cases proceed outside MDLs.
Does revision surgery qualify me for a lawsuit?
Yes — revision surgery is typically the primary qualifying event. Your original operative notes identifying mesh brand + surgeon's records of the revision procedure + explanation of why revision was needed (defect, infection, migration, etc.) are the critical evidence.
How is compensation calculated in hernia mesh settlements?
Honestly: no public schedule exists for the Bard settlement. This is an aggregate settlement negotiated privately between Becton Dickinson and plaintiffs' firms — not a class action — so there is no court-approved allocation plan on a public docket. BD's own SEC filings disclose no point values, no tiers and no per-claimant amounts, and the company states that its settlement activity "has resulted in confidential settlements … the terms of which may be confidential" (Form 10-Q filed August 6, 2026). The court's published order list for MDL 2846 contains dispositive-motion, case-management, discovery and pretrial orders only — no allocation order. Any site showing you a Bard point chart or per-point dollar value is publishing an unsourced estimate. Factors that plausibly drive individual valuations in mesh litigation generally — revision surgery, infection, bowel or visceral complications, chronic pain, lost wages — are matters your own attorney can weigh against the terms your firm actually negotiated. That is the only reliable source for your number.
What is the typical timeline to settlement?
Enrolled Bard plaintiffs: 2025-2027 distributions. Covidien: 2027+ estimated (after first bellwether July 2026). Individual state-court cases outside MDLs: 1-3 years typical. MDL-enrolled plaintiffs face longer timelines due to bellwether + mass settlement process.
Do I need my surgical records to file?
Yes — operative notes identifying mesh brand + revision surgery records are essential. Hospital records, pathology from mesh removal (if possible), device identification stickers in operative report. Without these, causation is difficult to establish.
Can I join if my mesh was placed years ago?
Yes, if within statute of limitations from discovery. Many cases date to early 2000s. Discovery rule typically tolls SOL until plaintiff knew or should have known mesh caused injury. Bard MDL tolling agreements may apply for previously enrolled plaintiffs.
Is Ethicon Physiomesh still accepting cases?
Very few remain (~16 active). Effectively resolved. New Ethicon cases unlikely to succeed due to SOL + resolved docket. Consult an attorney about state-court options.
What if my surgery was outside the US?
Claims must have been treated by US-licensed physicians with US venue connection. Foreign surgeries typically don't qualify for US MDLs. Some countries have their own mesh litigation (UK, Australia). Consult a product liability attorney in your jurisdiction.
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