Justia U.S. 8th Circuit Court of Appeals Opinion Summaries

Articles Posted in Products Liability
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Plaintiff filed a negligence and strict products liability suit against Stryker, the manufacturer and seller of the pain pump that was inserted into her shoulder to mitigate her pain while recovering from surgery. Plaintiff's husband filed a claim for loss of consortium. The court concluded that Stryker could not have foreseen the potential for articular cartilage damage as the result of the surgical implementation of its pain pump on the medical community's knowledge in 2002; Stryker, as a matter of law, had no duty to protect or warn plaintiff of the harm that Stryker's pain pumps may inflict; and the FDA denials did not indicate to Stryker that use of its pain pumps in intra-articular spaces was unsafe or could result in foreseeable harm. Accordingly, the court affirmed the district court's grant of summary judgment to Stryker. View "Mack, et al. v. Stryker Corp., et al." on Justia Law

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Plaintiff filed suit under 42 U.S.C. 1983 against the city and several police officers after her son was shot in the chest with an electronic control device (ECD). After the case settled, plaintiff filed suit against TASER for products liability and negligence. The court concluded that plaintiff's failure to warn claim failed as a matter of law because she did not establish on the record that an additional warning would have changed the behavior of the officers involved; the district court did not abuse its discretion in excluding plaintiff's expert's testimony on the issue of whether a different or additional warning would have altered the officer's actions under the existing circumstances; even if the court were to conclude that there was a legitimate jury question as to whether the officer had been made aware of the specific risk of cardiac danger when the ECD was fired directly at the subject's chest, such a conclusion would be rebuttable by undisputed evidence in the record that he had not been instructed on available warnings and did not heed the limited training he had received; there was no genuine dispute on the record that the officer would not have read any additional warning TASER may have added as to the cardiac danger of the ECD in any of its product warnings or bulletins, or in any training materials prepared after January 1, 2005; even if an adequate warning had appeared, the officer would not have heeded it; and therefore, TASER was entitled to summary judgment on plaintiff's negligence and failure to warn claims where she failed to establish that an additional warning would have altered the behavior of the officer. The court also concluded that plaintiff failed to present evidence that the ECD device used by the officer was unreasonably dangerous as designed. Plaintiff's design defect claim failed as a matter of law where plaintiff failed to demonstrate any "specific design choices" that rendered the model unreasonably dangerous. Accordingly, the court affirmed the district court's judgment and dismissed plaintiff's remaining claims as moot. View "Bachtel v. TASER Int'l, Inc." on Justia Law

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Plaintiff, after being diagnosed with tardive dyskinesia (TD), filed suit against Lilly, manufacturer of the antipsychotic drug, Zyprexa, alleging personal injury and product liability claims. The district court concluded that Lilly adequately warned plaintiff's treating and prescribing physicians of the risk of developing movement disorders like TD. On appeal, plaintiff argued, inter alia, that the district court erred in excluding his expert opinion testimony that 15% of Zyprexa users will develop TD after three years of use. The court concluded that the district court was well within its substantial discretion to conclude that plaintiff had not provided sufficient scientific support for the opinion and to exclude the opinion. The court also concluded that the district court properly applied the learned intermediary doctrine in dismissing the failure-to-warn claim. Finally, assuming Arkansas law recognized an overpromotion exception, the exception would not apply in this case because plaintiff presented no evidence that any representation by a salesperson affected a prescribing doctor's decision to continue plaintiff on Zyprexa and because there was no reliable evidence that Zyprexa had significantly more risk of movement disorders than the drug reps allegedly said it had. Accordingly, the court affirmed the district court's dismissal of plaintiff's complaint. View "Boehm v. Eli Lilly & Co." on Justia Law

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Plaintiff filed suit against Novartis alleging that Novartis negligently failed to provide adequate warnings for two drugs she took, Aredia and Zometa, after having two of her teeth extracted. Plaintiff developed osteonecrosis of the jaw (ONJ) after the extraction. Plaintiff was awarded $225,000 in compensatory damages and Novartis appealed. The court concluded that a jury could reasonably find that plaintiff's injury was the natural and probable consequence of Novartis's behavior and rejected Novartis's arguement that plaintiff did not establish that her injuries were proximately caused by inadequate warnings; the district court did not err in applying Missouri law where Missouri had the most significant relationship to the punitive damages claim; and Novartis correctly reasoned that the MedWatch checkmarks were inadmissible hearsay, out-of-court assertions offered for their truth but Novartis failed to demonstrate the prejudice required for a new trial. The court concluded, however, that the district court abused its discretion in awarding plaintiff full costs for depositions conducted as part of multi-district litigation. Accordingly, the court affirmed in Case No. 12-3121 and vacated in Case No. 12-3409. View "Winter v. Novartis Pharmaceuticals Corp." on Justia Law

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OMJP appealed from the district court's denial of its motion for relief from judgment under Federal Rule of Civil Procedure 60(b)(2) and (3). In Levaquin I, the court upheld a jury award in compensatory damages against OMJP for Achilles tendon injuries plaintiff suffered while taking OMJP's prescription antibiotic Levaquin. In this appeal, OMJP contended that the district court abused its discretion in denying OMJP relief under Rule (60)(b)(2) based on the delinquent and belated disclosure of an expert's calculation regarding the relative risk of Achilles tendon rupture to certain patients. The court concluded that the district court did not abuse its discretion in denying relief based on OMJP's claim of "newly discovered evidence" where the evidence was merely cumulative or impeaching and OMJP had not demonstrated that it was probable it would produce a different result. In regards to OMJP's misconduct claim under Rule 60(b)(3), the court concluded that the district court did not abuse its discretion in finding that the lack of the expert's calculation did not prevent OMJP from mounting a vigorous defense and that any misconduct did not warrant a new trial. Accordingly, the court affirmed the judgment of the district court. View "Schedin v. Ortho-McNeil-Janssen Pharmaceuticals" on Justia Law

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This case arose when groups of plaintiffs filed product liability actions against four manufacturers of transvaginal mesh devices, including Boston Scientific. Three groups filed similar motions proposing that the state court assign each group to a single Judge for purposes of discovery and trial. Two district judges granted plaintiffs' motions and remanded to state court on the ground that no case included more than 100 plaintiffs and plaintiffs had not proposed to the state court that the actions be tried jointly. The court granted Boston Scientific leave to appeal and vacated the order remanding to state court where the three groups of plaintiffs have already proposed to try their cases jointly within the meaning of the Class Action Fairness Act of 2005 (CAFA), 28 U.S.C. 1332(d)(11)(B)(i), because plaintiffs' counsel urged the state court to assign the claims of more than 100 plaintiffs to a single judge. View "Atwell, et al. v. Boston Scientific Corp." on Justia Law

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Bruce Martin filed suit against CTB for negligent misrepresentation and breach of express warranty after the power sweeps it purchased from CTB did not work. The court concluded that it's decision in Dannix Painting, LLC v. Sherwin-Williams foreclosed Bruce Martin's argument that the district court erred in concluding that Missouri's economic loss doctrine precluded its negligent misrepresentation claim. Further, the court concluded that the district court did not err in granting summary judgment to CTB on Bruce Martin's breach of express warranty claim. Under Indiana law, the court agreed with the district court that Bruce Martin had alleged a defect in the design of the sweeps that was not covered by CTB's warranty against "defects in material and workmanship." Accordingly, the court affirmed the judgment of the district court. View "Bruce Martin Construction, Inc. v. CTB, Inc." on Justia Law

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PETCO sought a declaration that ICNA had to defend and indemnify PETCO in an underlying litigation with Medtronic. Medtronic sued PETCO after an aquarium heater it had purchased from PETCO malfunctioned and started a fire at a Medtronic plant. The district court granted ICNA's motion for summary judgment and PETCO appealed. At issue was whether the aquarium heater satisfied a condition precedent to coverage under the policy. The court affirmed the district court's judgment on the ground that PETCO failed to identify any mandatory or voluntary safety standard with which the heater complied. View "PETCO Animal Supplies Stores, et al. v. Ins. Co. of North America" on Justia Law

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In this product liability suit against the manufacturers of the prescription drug Reglan and its generic equivalent (metoclopramide), plaintiff appealed the district court's adverse grant of summary judgment to Brand Defendants and its dismissal of her claims with prejudice against Generic Defendants. The court affirmed the district court's grant of summary judgment in favor of the Brand Defendants where plaintiff's claims were not viable under Arkansas law because she stipulated that she never used Reglan manufactured or distributed by any of the Brand Defendants. In regards to the claims against the Generic Defendants, the court reversed the dismissal of plaintiff's non-warning breach of implied warranty claims and remanded for further consideration as to whether they adequately stated viable claims under Arkansas law and if so, whether the Generic Defendants could nonetheless establish preemption. It was not immediately clear whether Arkansas offered generic drug manufacturers an opportunity, consistent with federal obligations to somehow alter an otherwise unreasonably dangerous drug. Accordingly, the court affirmed the district court's dismissal of plaintiff's failure to warn and failure to update claims; reversed the dismissal of plaintiff's non-warning design defect and breach of implied warrant claims; and remanded for further proceedings. View "Fullington v. Pfizer, Inc., et al." on Justia Law

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Plaintiff alleged various causes of action against the maker of the generic drug (Pliva), brand defendants, and others after she was injured by the prescription medication metoclopramide. On appeal, plaintiff challenged the district court's grant of summary judgment in favor of brand defendants and dismissal of her claims against Pliva. The court denied plaintiff's motion to supplement the record, finding no compelling reason to allow plaintiff to do so; the district court did not err in determining plaintiff's claims against brand defendants failed as a matter of law because she stipulated that she had not ingested a product manufactured by brand defendants; reversed the district court's dismissal of plaintiff's non-warning design defect and breach of implied warranty claims and remanded for further consideration; and because there was no causal link between Pliva's failure to incorporate the 2004 labeling change and plaintiff's injury, the district court's dismissal of that claim was not error. Accordingly, the court affirmed in part, reversed in part, and remanded for further proceedings. View "Bell v. Pfizer, et al." on Justia Law