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


Menu:
  •      Case: 09-31134     Document: 00511196661          Page: 1    Date Filed: 08/06/2010
    IN THE UNITED STATES COURT OF APPEALS
    FOR THE FIFTH CIRCUIT  United States Court of Appeals
    Fifth Circuit
    FILED
    August 6, 2010
    No. 09-31134                         Lyle W. Cayce
    Clerk
    RUTH CARTER; JAMES CARTER,
    Plaintiffs-Appellants
    v.
    MATRIXX INITIATIVES, INC.; ZICAM, L.L.C.,
    Defendants-Appellees
    Appeal from the United States District Court
    for the Middle District of Louisiana
    USDC No. 3:08-cv-00216
    Before SMITH, WIENER, and ELROD, Circuit Judges.
    PER CURIAM:*
    Plaintiffs-Appellents Ruth and James Carter (collectively, the “Carters”
    or “Carter”) 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,
    *
    Pursuant to 5TH CIR . R. 47.5, the court has determined that this opinion should not
    be published and is not precedent except under the limited circumstances set forth in 5TH CIR .
    R. 47.5.4.
    Case: 09-31134    Document: 00511196661      Page: 2   Date Filed: 08/06/2010
    No. 09-31134
    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 Zicam.”
    The Carters filed the instant suit on February 29, 2008 in the 21st Judicial
    District Court, Parish of Livingston, Louisiana, against Defendants-Appellees
    Matrixx 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.
    2
    Case: 09-31134         Document: 00511196661        Page: 3     Date Filed: 08/06/2010
    No. 09-31134
    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 Act2 “establishes the exclusive theories
    of liability for manufacturers for damage caused by their products.”3 L A. C IV.
    C ODE art. 3492 establishes a one-year prescriptive period for products liability
    claims:
    Delictual actions are subject to a liberative prescription of one year. This
    prescription commences to run from the 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 praescriptio 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
    1
    LaBarge Pipe & Steel Co. v. First Bank, 
    550 F.3d 442
    , 449 (5th Cir. 2008).
    2
    LA . REV .STAT . § 9:2800.51 et seq.
    3
    
    Id. at §
    9:2800.52.
    4
    Sharkey v. Sterling Drug, Inc., 
    600 So. 2d 701
    , 713 (La. App. Ct. 1st Cir. 1992).
    3
    Case: 09-31134        Document: 00511196661         Page: 4       Date Filed: 08/06/2010
    No. 09-31134
    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 plaintiff’s 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 23, 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
    5
    
    Id. 6 Cole
    v. Celotex Corp., 
    620 So. 2d 1154
    , 1156 (La. 1993).
    7
    Jordan v. Employee Transfer Corp., 
    509 So. 2d 420
    , 423 (La. 1987) (emphasis added).
    8
    
    Sharkey, 600 So. 2d at 713-14
    .
    4
    Case: 09-31134         Document: 00511196661        Page: 5     Date Filed: 08/06/2010
    No. 09-31134
    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 and the putative tortfeasor is
    established. 9 Rather, actual or constructive knowledge 10 of the “tortious act, the
    resulting injury, and the causal connection between the two”11 is the benchmark
    for beginning the prescriptive period. Carter experienced “excruciating” pain
    immediately after using Zicam on February 23, 2007, and evinced a firm,
    unwavering, and objectively reasonable belief no later than the next day,
    February 24, that Zicam was the cause of her suffering.                      Therefore, the
    prescriptive period began running on February 23 (February 24 at the latest).
    Thus, the Carters’ filing was at least five days late.
    The judgment of the district court is, in all respects, AFFIRMED.
    9
    See Luckett v. Delta Airlines, Inc., 
    171 F.3d 295
    , 299-300 (5th Cir. 1999) (“The
    commencement of prescription does not necessarily wait for the pronouncement of a victim’s
    physician or of an expert.”) (citing Hunter v. Sisters of Charity of the Incarnate Word, 
    236 So. 2d
    565, 568 (La. App. 1st Cir. 1970)).
    10
    See 
    id. 11 Sharkey,
    600 So. 2d at 714.
    5
    

Document Info

Docket Number: 09-31134

Citation Numbers: 391 F. App'x 343

Judges: Smith, Wiener, Elrod

Filed Date: 8/6/2010

Precedential Status: Non-Precedential

Modified Date: 11/5/2024