Justia U.S. 5th Circuit Court of Appeals Opinion Summaries

In 2018, a $200 million mixed-use development project at Louisiana State University experienced issues with its fire-protection sprinkler systems, which began to crack and leak. Allied World National Assurance Company, which paid over $10 million for system replacements, sued Nisus Corporation in 2021, alleging that Nisus falsely represented its product's compatibility with the pipe material, leading to the damage.The United States District Court for the Middle District of Louisiana granted summary judgment in favor of Nisus, concluding that Allied's claims were time-barred under Louisiana law. The court found that while Provident, the insured party, did not have actual or constructive knowledge of the cause of the damage, RISE Residential, Provident's agent, had constructive knowledge of the cause by November 2019. This knowledge was imputed to Provident, starting the prescription period.The United States Court of Appeals for the Fifth Circuit reviewed the case de novo and affirmed the district court's decision. The court held that RISE Residential's constructive knowledge of the sprinkler system issues, which was imputed to Provident, triggered the running of the prescription period well before July 23, 2020. The court also found that Nisus did not prevent Allied from timely availing itself of its causes of action, as a reasonable inquiry by RISE Residential would have uncovered the necessary information. Therefore, Allied's claims were prescribed, and the summary judgment in favor of Nisus was affirmed. View "Allied World National v. Nisus" on Justia Law

In 2021, Grant and Sarah Palmquist, on behalf of their minor son, sued baby-food manufacturer Hain Celestial Group, Inc. and grocery retailer Whole Foods Market, Inc. in Texas state court. They sought damages for their son Ethan’s physical and mental decline, which they allege began when he was about thirty months old and had been consuming Hain’s Earth’s Best Organic Products, purchased from Whole Foods. The Palmquists attributed Ethan's health issues to heavy metal toxicity caused by the baby food. The case was removed to federal court, where Whole Foods was dismissed as improperly joined and judgment was granted in favor of Hain during trial.The district court dismissed Whole Foods on the grounds of improper joinder and denied the Palmquists’ motion to remand the case to state court. The court also granted Hain’s motion for judgment as a matter of law, concluding that the Palmquists had presented no evidence of general causation. The Palmquists appealed these decisions.The United States Court of Appeals for the Fifth Circuit reversed the district court’s judgment denying the Palmquists’ motion to remand, vacated the final judgment of the district court, and remanded with instructions for the district court to remand the case to the state court. The court held that the Palmquists were entitled to a remand to state court because the allegations in their state-court complaint stated plausible claims against Whole Foods. The court did not address whether the district court erred in granting judgment as a matter of law in favor of Hain. View "Palmquist v. Hain Celestial Group" on Justia Law

The case involves four plaintiffs who took docetaxel, a chemotherapy drug, as part of their treatment for early-stage breast cancer and subsequently suffered permanent chemotherapy-induced alopecia (PCIA). The plaintiffs allege that the manufacturers of the drug, Hospira, Inc., Hospira Worldwide, LLC, and Accord Healthcare, Inc., violated state law by failing to warn them that docetaxel could cause PCIA.The case was initially heard in the United States District Court for the Eastern District of Louisiana, where the defendants moved for summary judgment on the basis that the plaintiffs' state law failure-to-warn claims were preempted by federal law. The district court denied the motion, and the defendants appealed.The United States Court of Appeals for the Fifth Circuit was tasked with determining whether federal law preempts the plaintiffs' state law failure-to-warn claims against the defendant drug manufacturers. The court found that the district court had erred in its interpretation of what constitutes "newly acquired information" under the changes-being-effected (CBE) regulation, which allows manufacturers to file a supplemental application with the FDA and simultaneously implement a labeling change before obtaining FDA approval. The court held that the district court failed to enforce the requirement that newly acquired information must "reveal risks of a different type or greater severity or frequency than previously included in submissions to FDA."The court vacated the district court's judgment on the plaintiffs' failure-to-warn claims and remanded the case for further consideration of one outstanding issue: whether the Bertrand Abstract, a scientific study, constituted "newly acquired information" that revealed a greater risk of PCIA than previously known. If the Bertrand Abstract does not meet this standard, the court held that the defendants would not be liable to the plaintiffs on their state law failure-to-warn claims. View "Hickey v. Hospira" on Justia Law

In this case, the United States Court of Appeals for the Fifth Circuit reversed a verdict from the United States District Court for the Northern District of Texas. The plaintiffs, C. Sidney Johnston and Danette Johnston, had sued Ferrellgas, Incorporated after Mr. Johnston was injured using a propane tank manufactured by Ferrellgas. A jury had found Ferrellgas liable for a manufacturing defect and negligence and awarded the Johnstons $7 million, which the district court reduced to $1.7 million. On appeal, Ferrellgas contended that the district court erred in denying its motion for judgment as a matter of law because there was insufficient evidence to support the verdict.The Court of Appeals agreed with Ferrellgas. The Court found that there was no substantial evidence to support the jury's finding that the tank was defective when it left Ferrellgas's possession, a crucial element of a manufacturing defect claim. The Court also found that the negligence claim must fail, as it was dependent on the tank having a manufacturing defect.The Court therefore reversed the district court's denial of Ferrellgas's motion for judgment as a matter of law on both the manufacturing defect and negligence claims, and rendered judgment for Ferrellgas. View "Johnston v. Ferrellgas" on Justia Law

In this diversity case, Plaintiff sued Biomet Inc. and Zimmer, Inc. (collectively, “Biomet”) under the Louisiana Products Liability Act (“LPLA”). The district court found Plaintiff’s claims were prescribed and granted summary judgment in favor of Biomet.   The Fifth Circuit vacated the district court’s summary judgment order and remanded for further proceedings consistent with this opinion, including any additional discovery the district court may order. The court explained that given Plaintiff’s consultations with his doctor, a medical professional. But on the other hand, a jury could just as reasonably determine that contra non valentem tolled prescription until some point in time before September 2019. It is unclear whether Plaintiff stopped suffering complications from infections after the removal, such that his recovery after the device’s removal would have put him on notice of any fault of Biomet’s before the letter was received. As the record stands, when the prescriptive period expired, and whether contra non valentum applies, is a question best left for the jury. View "Bruno v. Biomet" on Justia Law

Defendant appealed his sentence following his guilty-plea conviction of felon in possession of a firearm. He argued that the district court erred in enhancing his sentence under U.S.S.G. Section 2K2.1(b)(4)(B), which applies only when a defendant’s firearm “had an altered or obliterated serial number,” because there is no evidence that his rifle ever had a serial number.   The Fifth Circuit agreed and vacated Defendant’s sentence and remanded. The court explained that it agreed that Section 2K2.1(b)(4)(B) does not apply when there is no evidence that the firearm ever had a serial number. The text of Section 2K2.1(b)(4)(B) is clear that it only applies when the firearm “had an altered or obliterated serial number.” U.S.S.G. Section 2K2.1(b)(4)(B). And in ordinary parlance, something cannot be “altered or obliterated” if it never existed in the first place. Consequently, to apply an upward enhancement under the provision, the government must present evidence showing that Defendant’s rifle once had a serial number. Because there was no such evidence, the court held that the district court erred in applying a four-level enhancement under Section 2K2.1(b)(4)(B). View "USA v. Sharp" on Justia Law

Fourteen women (“Plaintiffs”) from seven states brought the present putative class action against Ashley Black and her companies (“Defendants”), alleging false and deceptive marketing practices. They take issue with various representations in Defendants’ ads about a product called the FasciaBlaster, a two-foot stick with hard prongs that is registered with the Food and Drug Administration as a massager. The district court dismissed Plaintiffs’ claims in their entirety.  Plaintiffs appealed the order striking the class allegations and the dismissal of individual claims.   The Fifth Circuit found that the district court correctly struck Plaintiffs’ class allegations and properly dismissed all but two of their claims. Accordingly, the court affirmed in part, reversed in part, and remanded the case to the district court. The court explained that it agreed with the district court that Plaintiffs’ allegations suffer from a combination of defects, including a failure to plead adequately what representations were actually made when those representations were made, who made the representations, and where those representations occurred.   However, the court reversed the dismissal of Plaintiffs’ breach of express warranty under, respectively, California Consumer Code Sections 2313 & 10210, and Florida Statutes Sections 672.313 & 680.21. The court wrote that the district court did not apply the law of a specific jurisdiction when conducting its analysis. Plaintiffs on appeal cite various Fifth Circuit cases in addition to Texas and California state law precedents. Defendants proffer Fifth Circuit, California, and Florida precedents. Neither party, however, briefed what law should be applied to each claim. View "Elson v. Black" on Justia Law

In June 2011, a fifteen-year-old shot his brother, an eleven-year-old, with a Remington Model 700 rifle equipped with an X-Mark Pro trigger. The boy and his parents (collectively, “Plaintiffs”) sued Remington, the retailer that sold the rifle, and Remington’s predecessors in interest (collectively, “Defendants”) in Mississippi state court. Plaintiffs emphasized that Remington had in April 2014 recalled all Model 700 rifles with X-Mark Pro triggers because the rifles “can and will spontaneously fire without pulling the trigger.” They brought state-law claims for product liability, failure to warn, negligence, and gross negligence.   Defendants moved to dismiss under Rule 12(b)(6). In their response to that motion, Plaintiffs asked to file a federal-court complaint to allege additional facts related to the statute of limitations. The Fifth Circuit affirmed. The court explained that the district court’s subject-matter jurisdiction was based on diversity of citizenship. The court, therefore, applied “federal procedural and evidentiary rules and the substantive laws of the forum state.” Mississippi has a general three-year statute of limitations. For “non-latent injuries” like the one alleged here, the cause of action accrues on the date of the injury. But Plaintiffs, who filed suit in March 2018, argue that the statute of limitations was tolled by Defendants’ fraudulent concealment. The district court rejected that argument. The Fifth Circuit agreed, finding that Plaintiffs failed to meet Rule 9(b)’s requirements. View "Stringer, et al v. Remington Arms, et al" on Justia Law

Plaintiffs sued Defendants, C.R. Bard, Inc. and Bard Peripheral Vascular, Inc. (“Bard”), due to complications Plaintiff experienced after implantation of a filter used as a medical device. The Plaintiffs now appeal the district court’s grant of summary judgment to Bard on their failure to warn and design defect claims.The Fifth Circuit affirmed. The court explained that n a failure-to-warn case, a plaintiff must show by the preponderance of the evidence that the product was defective because it failed to contain adequate warnings or instructions, the defective condition rendered the product unreasonably dangerous to the user or consumer, and the defective and unreasonably dangerous condition of the product proximately caused the damages for which recovery is sought.Here, Bard’s warning label warned in two different locations that Filter fracture and migration were “known complication[s].” Plaintiffs have thus failed to raise a genuine issue of material fact as to their failure to warn claim.Further, the court wrote that Plaintiffs make broad statements throughout their brief that presume a design defect must have caused Plaintiff’s complications. But actual evidence had to be identified to the district court in order to advance beyond the summary judgment stage for a design defect claim. View "Nelson v. C. R. Bard, Incorporated" on Justia Law

Plaintiffs seek to hold Bodum USA, Inc., responsible for an alleged manufacturing defect in one of its French press coffee makers (“the Press”) that they claim caused it to malfunction and injure their young child. The district court granted summary judgment for Bodum, concluding that no reasonable jury could find that the Press deviated from its intended design.The Fifth Circuit reversed and remanded. The court explained that a manufacturing defect may be established exclusively through circumstantial evidence and plaintiffs must allege a specific deviation from the product’s intended design that allegedly caused the injury. Here, Plaintiffs show the alleged defect was present when the Press left Bodum’s control, Plaintiffs point to French press coil assemblies advertised on Bodum’s website that also contain an outwardly protruding coil. Moreover, the court wrote that the following evidence creates a genuine issue of material fact as to whether the Press contained a manufacturing defect: (1) testimony from Plaintiffs that they purchased their Press in brand-new condition; (2) a specific alleged defect consisting of a metal coil protruding beyond its mesh enclosure; (3) the district court’s finding that “the metal mesh was intended to completely engulf the metal coil,” which is corroborated by expert testimony; (4) an expert witness who examined the Press, tested it, compared it with two exemplars, and opined that the protruding metal coil deviated from the Press’s intended design, and caused the glass to fracture and ultimately shatter; and (5) the shattering of the Press’s glass carafe allegedly during ordinary use, albeit by a five-year-old child. View "Norman v. Bodum USA" on Justia Law