Statute of Limitations
Ohio Revised Code § 2305.10 imposes a 2-year statute of limitations for product liability claims, measured from the date of discovery of the injury (discovery rule applies). Ohio has a 10-year statute of repose for product liability running from the date of first sale of the product to the plaintiff (ORC § 2305.10(C)). Patients implanted with mesh products first sold before 2016 face potential repose exposure and should consult an attorney immediately.
2 years from discovery; 10-year statute of repose from product first sale
Where to File in Ohio
Ohio occupies a unique position in hernia mesh litigation: it is the home district of both major federal MDLs. Davol/CR Bard MDL 2846 and Covidien Parietex MDL 2511 are both pending before Judge Edmund Sargus in the Southern District of Ohio (Cincinnati). Ohio plaintiffs can file directly in S.D. Ohio without a tag-along transfer. Atrium C-QUR cases go to MDL 2753 in D.N.H., and Ethicon cases to the Atlantic County NJ Superior Court mass tort.
Ohio's statute of limitations for products liability is two years from the date of discovery under Ohio Rev. Code § 2305.10. Ohio applies the discovery rule: the cause of action accrues when the plaintiff discovers, or in the exercise of reasonable diligence should have discovered, the injury and its cause. Ohio courts have found that mesh injuries presenting as chronic pain, infection, or bowel obstruction years after implantation warrant delayed accrual, making the discovery rule especially important for Ohio mesh claimants.
As home to Judge Sargus and both major MDLs, Ohio holds particular strategic significance. Cincinnati, Columbus, Cleveland, and Dayton are major hernia surgical hubs. The Cleveland Clinic and Ohio State Wexner Medical Center are high-volume mesh implant centers. Ohio plaintiffs benefit from the convenience of direct filing in S.D. Ohio for Bard and Covidien cases, with no transfer delay. Bard Davol's Composix L/P, Ventralight, and PerFix products are the most-litigated Ohio-implanted devices.
Ohio's role as the MDL seat means local counsel have developed strong MDL practice infrastructure in Columbus and Cincinnati. For Ethicon/J&J claims, Ohio plaintiffs must file in Atlantic County NJ state court or have their state court cases transferred to the New Jersey mass tort. Judge Porto's docket accepts all Physiomesh and Prolene Hernia System claims regardless of the plaintiff's home state.
Exposure in Ohio
Source: U.S. District Court, S.D. Ohio
Source: ORC § 2305.10(C)
Source: Ohio Department of Health hospital data
Clinics & Specialists in Ohio
Cleveland Clinic — Digestive Disease and Surgery Institute, Hernia Center
The Ohio State University Wexner Medical Center — Minimally Invasive Surgery Program
Your Legal Team
Robert Kaufman
Senior Partner
Columbus, OH
Robert Kaufman has spent 19 years at the center of medical device mass tort litigation, with a practice anchored in the Southern District of Ohio — the forum for MDL 2846. His proximity to and familiarity with the MDL court, case management orders, and Plaintiff Steering Committee processes provides clients with strategic advantages from day one. Robert has represented over 400 hernia mesh claimants and served as local counsel for out-of-state firms navigating MDL 2846 practice requirements. He is known for meticulous Plaintiff Fact Sheet preparation — a skill that directly affects claim tier placement and settlement value. Robert is a member of the American Association for Justice Mass Tort Litigation Group and a frequent presenter at mass tort conference panels on MDL 2846 developments.
Education
- J.D., Ohio State University Moritz College of Law (2007)
- B.S., Biology, Case Western Reserve University (2004)