Ruth Carter v. Matrixx Initiatives, Inc., e

391 F. App'x 343
CourtCourt of Appeals for the Fifth Circuit
DecidedAugust 6, 2010
Docket09-31134
StatusUnpublished
Cited by2 cases

This text of 391 F. App'x 343 (Ruth Carter v. Matrixx Initiatives, Inc., e) is published on Counsel Stack Legal Research, covering Court of Appeals for the Fifth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ruth Carter v. Matrixx Initiatives, Inc., e, 391 F. App'x 343 (5th Cir. 2010).

Opinion

PER CURIAM: *

Plaintiffs-Appellants Ruth and James Carter (collectively, the “Carters” or “Car *344 ter”) appeal the district court’s grant of summary judgment dismissing their products liability and loss of consortium claims. We affirm.

I. FACTS AND PROCEEDINGS

The facts of this case are undisputed. On February 23, 2007, Ruth Carter used Zicam No Drip Liquid Nasal Gel Cold Remedy and immediately experienced “immediate,” “blind[ing],” and “excruciating” pain. The next day, Carter realized that she had lost her senses of smell and taste and, because of the continuing pain, did not report to work. She told her husband and her employees that she either had “a heck of an allergy” or “the Zicam” had burned her nasal passages. Her loss of sensory ability and pain continued until she saw her primary care physician on March 2, 2007. During the appointment she reported her suspicion that the Zicam was the cause of her discomfort; her physician did not confirm or deny this, except to note he was unaware that Zicam caused such problems, but he did suggest that Carter’s injury may have been caused by her allergies. Carter’s symptoms did not improve, so she was referred to a radiography center to image her nasal passages. During the imaging on May 7, 2007, Carter told a radiography technician about her suspicions regarding Zicam, to which the technician responded that she had received an e-mail communication warning “to be on the lookout for this problem with Zi-cam.”

The Carters filed the instant suit on February 29, 2008 in the 21st Judicial District Court, Parish of Livingston, Louisiana, against Defendants-Appellees Ma-trixx Initiatives, Inc. and Zicam, L.L.C. (collectively, “Matrixx”) alleging damages for various claims, including personal injury and loss of consortium resulting from Ruth Carter’s use of the Zicam homeopathic nasal remedy. After the Carter’s action was removed to federal district court on diversity grounds and all claims other than those allowed under the Louisiana Products Liability Act were dismissed, Matrixx filed a motion for summary judgment seeking dismissal of the Carters’ remaining claims. Matrixx argued that because the action was filed six days after the expiration of Louisiana’s one-year prescriptive period for products liability suits, it should be dismissed. The district court granted summary judgment on this ground, and the Carters timely appealed.

II. ANALYSIS

We apply a de novo standard of review when determining whether a district court erred in granting summary judgment. 1 Under Federal Rule of Civil Procedure 56(c)(2), summary judgment “should be rendered if the pleadings, the discovery and disclosure materials on file, and any affidavits show that there is no genuine issue as to any material fact and that the movant is entitled to judgment as a matter of law.”

The Louisiana Products Liability Act 2 “establishes the exclusive theories of liability for manufacturers for damage caused by their products.” 3 La. Civ.Code art. 3492 establishes a one-year prescriptive period for products liability claims:

Delictual actions are subject to a libera-tive prescription of one year. This prescription commences to run from the *345 day injury or damage is sustained. It does not run against minors or interdicts in actions involving permanent disability and brought pursuant to the Louisiana Products Liability Act or state law governing product liability actions in effect at the time of the injury or damage.

By filing the complaint on February 29, 2008 — six days after the one-year anniversary of Ruth Carter’s sustaining her initial injury — the Carters’ suit falls outside of the prescriptive period. The Carters nevertheless insist that the doctrine of contra non valentem agere nulla currit praes-criptio applies. Under that doctrine, “prescription does not commence running until the facts necessary to state a cause of action are known or reasonably knowable to the plaintiff.” 4 “In such cases of [medical causation], even if a plaintiff is aware that an undesirable condition developed at some point in time after medical treatment, prescription does not run until the plaintiff has actual or constructive notice of the causal connection between the medical treatment and the subsequent condition.” 5 “Damage is considered to have been sustained, within the meaning of the article, only when it has manifested itself with sufficient certainty to support accrual of a cause of action.” 6 Furthermore:

prescription will not begin to run at the earliest possible indication that a plaintiff may have suffered some wrong. Prescription should not be used to force a person who believes he may have been damaged in some way to rush to file suit against all parties who might have caused that damage. On the other hand, a plaintiff will be responsible to seek out those whom he believes may be responsible for a specific injury. When prescription begins to run depends on the reasonableness of a plaintiff’s action or inaction. 7

When a plaintiff alleges the affirmative defense of contra non valentem, the defendant must show “that the plaintiff had actual or constructive notice of the tortious act, the resulting injury, and the causal connection between the two or that the plaintiffs lack of such knowledge was willful, negligent or unreasonable.” 8

It is apparent that Carter first sustained the injury that allegedly resulted from her use of Zicam on February 28, 2007 and that she had actual knowledge of pain and sensory loss on that same day. From the very outset, Carter suspected and attributed her injury to Zicam, and she never wavered in that belief. That she did not possess an affirmative and conclusive medical opinion supporting this belief on that day, or even a week later when she consulted her physician, is of no moment. On February 24 at the latest, Carter indisputably had both the belief that Zicam was the cause of her injuries and a reasonable basis for seeking to hold the manufacturer responsible. It is true that her doctor initially expressed ambivalence about whether it was the Zicam or Carter’s allergies that were causing her injury and that she did not receive any kind of cause-and-effect corroboration from a third party until she heard about the technician’s email on May 7. It is not the rule in Louisiana, however, that the prescriptive period does not begin until conclusive, dispositive proof of a causal connection between the suspected injury *346

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Bluebook (online)
391 F. App'x 343, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ruth-carter-v-matrixx-initiatives-inc-e-ca5-2010.