Justia Products Liability Opinion Summaries

Timothy Davis accidentally shot himself in the leg with his Sig Sauer P320 X-Carry pistol while getting out of his truck. Davis claimed the gun was fully holstered and that he did not pull the trigger. He alleged that the P320 was defectively designed, making it prone to accidental discharge, and that alternative designs could have prevented his injury. Davis filed a products-liability lawsuit against Sig Sauer under Kentucky law, citing strict liability and negligence.The United States District Court for the Eastern District of Kentucky granted Sig Sauer’s motions to exclude Davis’s expert witnesses and for summary judgment. The court found that Davis’s experts, James Tertin and Dr. William J. Vigilante, Jr., did not investigate the exact circumstances of the shooting and thus could not opine on causation. Without expert testimony, the court held that Davis could not pursue his products-liability claims.The United States Court of Appeals for the Sixth Circuit reviewed the case. The court affirmed the district court’s exclusion of the experts’ opinions on causation but reversed the exclusion of their testimonies on design defects and reasonable alternative designs. The appellate court found that the experts’ opinions were admissible to prove that the P320 was defectively designed and that reasonable alternative designs existed. The court held that Davis had demonstrated a genuine issue of material fact regarding whether the P320 was defectively designed and caused his injury. Consequently, the court vacated the district court’s grant of summary judgment and remanded the case for further proceedings. View "Davis v. Sig Sauer, Inc." on Justia Law

Jackson died in a car accident on U.S. Highway 70 after he lost control of his 2012 Ford Focus. Mrs. Jackson, who was a passenger in the car, was seriously injured. She sued, alleging that Ford was responsible for the accident because it equipped the car with a defective “Electronic Power Assisted Steering” (EPAS) system that caused the loss of control. The district court dismissed, finding that Jackson did not adequately plead proximate cause. The Seventh Circuit reversed, stating that “the district court demanded too much of Jackson under the familiar Iqbal and Twombly pleading requirements.” Jackson plausibly alleged that a defect in the 2012 Ford Focus’s EPAS system was a substantial factor in bringing about the accident, as is apparent from the litany of other accidents identified by Jackson where the EPAS system allegedly failed, causing the driver to lose control of the vehicle. Ford’s “hypertechnical arguments regarding the allegations” in Jackson’s complaint rest on an inaccurate understanding of notice pleading. View "Jackson v. Ford Motor Co." on Justia Law

In the 1990s, Stryker purchased a Pfizer subsidiary that made orthopedic products, including the “Uni-knee” artificial joint. It was later discovered that those devices were sterilized using gamma rays, which caused polyethylene to degrade. If implanted past their five-year shelf-life, the knees could fail. Expired Uni-Knees were implanted in patients. Stryker, facing individual product-liability claims and potentially liable to Pfizer, sought defense and indemnification under a $15 million XL “commercial umbrella” policy, and a TIG “excess liability” policy that kicked in after the umbrella policy was fully “exhausted.” XL denied coverage, arguing that the Uni-Knee claims were “known or suspected” before the inception of the policy. Stryker filed lawsuits against the insurers, then unilaterally settled its individual product-liability claims for $7.6 million. Stryker was adjudicated liable to Pfizer for $17.7 million. About 10 years later, the Sixth Circuit held that XL was obliged to provide coverage. XL paid out the Pfizer judgment first, exhausting coverage limits. TIG declined to pay the remaining $7.6 million, arguing that Stryker failed to obtain “written consent” at the time the settlements were made. Stryker claimed that the policy was latently ambiguous because XL satisfied the Pfizer judgment first, Stryker was forced to present its settlements to TIG years after they were made. The district court granted Stryker summary judgment. The Sixth Circuit reversed, finding the contract unambiguous in requiring consent. View "Stryker Corp. v. National Union Fire Insurance Co." on Justia Law

The American husband and German wife have lived together in Germany since 2002. They sought damages for complications that arose when a surgical stapler manufactured in Mexico by an American corporation, Ethicon, allegedly malfunctioned during a 2012 surgery that husband underwent in Germany. An Ohio district court dismissed on the ground of forum non conveniens in favor of litigating in Germany. The Sixth Circuit affirmed. Where a district court has considered all relevant public- and private-interest factors, and has reasonably balanced those factors, its decision deserves substantial deference. Private-interest factors include the relative ease of access to sources of proof; availability of compulsory process and the cost of obtaining witnesses; possibility of view of premises, id appropriate; and all other practical problems. Public-interest factors include administrative difficulties from court congestion; the local interest in the controversy’; the interest in having the trial in a forum that is at home with the law that governs the action; and the unfairness of burdening citizens in an unrelated forum with jury duty. The court here correctly concluded that Ethicon met its burden of showing that if the case remained in Ohio, the vexation it would endure and trouble to the court would be disproportionate to the plaintiffs’ minimal convenience. View "Hefferan v. Ethicon Endo-Surgery, Inc." on Justia Law

While working amidst a high-wall mining (HWM) system at Southern Coal’s Harlan County mine, Smith, disengaging a conveyor car from the system, inadvertently placed his foot in a “pinch point” that existed between a hydraulic pusher used to launch cars into the mine and an outer guide rail on the mining platform. When the hydraulic pusher was prematurely activated by another worker, it crushed Smith’s foot against the guide rail. The injury resulted in the amputation of his lower left leg. In Smith’s suit, alleging negligence and strict liability for defective design and failure to warn, a jury returned a verdict in favor of the HWM manufacturer (Joy). The Sixth Circuit affirmed, rejecting Smith's arguments that the district court erred by instructing the jury that Joy could be liable for negligent failure to warn only if Smith was unaware of the danger he faced and regarding a rebuttable presumption of nondefectiveness. The court declined a request to certify to the Kentucky Supreme Court questions of state law concerning both of those jury instructions. View "Smith v. Joy Techs., Inc." on Justia Law

In 2004, Yates, 17 years old, was sexually active and was suffering from severe menstrual cramps. Smith, a licensed physician assistant, counseled Yates about various contraceptives, and the risks and benefits accompanying each. Yates admits that she was counseled concerning the risk of a stroke and clotting associated with ORTHO EVRA®. She decided to try Depo-Provera, which requires injections at three-month intervals. In 2005 she discontinued Depo-Provera due to weight gain and switched to the ORTHO EVRA® patch. Smith again discussed side effects. Yates admitted that she would have used ORTHO EVRA® even if she had read package warnings. Yates suffered a stroke while she was wearing her first weekly patch. A board-certified neurologist and neurophysiologist opined that Yates’s “use of the Ortho-Evra patch was the contributing cause of her stroke.” Smith’s suit was transferred for consolidated pretrial proceedings in connection with In re: Ortho Evra Products Liability Litigation. The district court dismissed her claims. The Sixth Circuit affirmed. The ORTHO EVRA® warnings in effect when Yates was prescribed the patch adequately warned her prescribing medical provider of the risk of stroke; there was no duty to directly warn Yates. The court rejected design defect, manufacturing defect, and negligence claims. View "Yates v. Ortho-McNeil-Janssen Pharma., Inc." on Justia Law