In Re Diet Drugs (Phentermine/Fenfluramine/Dexfenfluramine) Products Liability Litigation ( 2013 )


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  •                                                                    NOT PRECEDENTIAL
    UNITED STATES COURT OF APPEALS
    FOR THE THIRD CIRCUIT
    ________________
    No. 12-3138
    ________________
    IN RE: DIET DRUGS (PHENTERMINE/FENFLURAMINE/DEXFENFLURAMINE)
    PRODUCTS LIABITY LITIGATION
    Roberta Haberman,
    Appellant
    ________________
    Appeal from the United States District Court
    for the Eastern District of Pennsylvania
    (D.C. Civil Action Nos. 2-99-cv-20593/ 2-12-MD-01203)
    District Judge: Honorable Harvey Bartle, III
    ________________
    Argued March 5, 2013
    Before: RENDELL, AMBRO, and VANASKIE, Circuit Judges
    (Opinion filed: May 21, 2013)
    Howard J. Bashman, Esquire
    Suite G-22
    2300 Computer Avenue
    Willow Grove, PA 19090
    Stanley D. Hudson, Esquire
    Kip A. Petroff, Esquire (Argued)
    Petroff & Associates
    3838 Oak Lawn Avenue, Suite 1620
    Dallas, TX 75219
    Counsel for Appellant
    Geoffrey J. Michael, Esquire
    Arnold & Porter
    555 Twelfth Street, N.W.
    Washington, DC 20004
    Raymond M. Williams, Esquire
    DLA Piper
    1650 Market Street
    One Liberty Place, Suite 4900
    Philadelphia, PA 19103
    Jules S. Henshell, Esquire (Argued)
    Semanoff, Ormsby, Greenberg & Torchia
    2617 Huntingdon Pike
    Huntingdon Valley, PA 19006
    Laurence S. Berman, Esquire
    Michael D. Fishbein, Esquire
    Arnold Levin, Esquire
    Levin, Fishbein, Sedran & Berman
    510 Walnut Street, Suite 500
    Philadelphia, PA 19106
    Charles R. Parker, Esquire
    Yetter & Coleman
    909 Fannin Street, Suite 3600
    Houston, TX 77010
    Counsel for Appellees
    ________________
    OPINION
    ________________
    AMBRO, Circuit Judge
    In November 1999, Wyeth L.L.C. (―Wyeth‖) entered into a nationwide class
    action settlement agreement (the ―Settlement Agreement‖) related to its marketing of two
    weight-loss agents, fenfluramine/phentermine (known as ―fen-phen‖) and
    dexfenfluramine, linked to the development of valvular heart disease. When a patient
    2
    suffers from this condition, blood that is supposed to move in a forward direction through
    the heart leaks backward, or regurgitates, through the diseased valve. However, as the
    parties acknowledge, other factors can also cause or contribute to the development of this
    medical problem; we refer to these as alternative causation factors.
    Under the Settlement Agreement, qualifying diet drug users suffering from
    valvular heart disease receive compensation based on their age and the severity level of
    their medical condition. In general, to qualify for these benefits, a claimant must be
    diagnosed as FDA Positive (having a requisite level of valvular regurgitation).
    The Settlement Agreement has two payment matrices—Matrix A (which provides
    greater compensation) and Matrix B (which provides lesser compensation)—that are used
    to calculate the compensation a claimant will receive.1 Matrix A applies to claimants
    who ingested diet drugs for fewer than 61 days and do not have any of the alternative
    causation factors listed by the Settlement Agreement. Matrix B applies to resolve all
    other qualifying claims. Claimants whose valvular heart conditions worsen to a higher
    severity level are permitted to file supplemental claims seeking additional benefits.
    In 2010, Roberta Haberman—a class member who previously received
    compensation under the Settlement Agreement because she suffered from valvular heart
    disease2—filed a supplemental claim after undergoing dual heart valve surgery in 2009.
    1
    Each Matrix has five severity levels and 11 age groups that determine the amount due to
    the claimant.
    2
    In 2004, the Settlement Agreement was amended to establish a streamlined process for
    resolving the large number of low-level severity claims that had been filed by putative
    class members. The amendment did not use the payment matrices to determine the
    amount due to each claimant. Instead, claimants received a pro rata distribution from a
    3
    In her supplemental claim form, she asserted that she was entitled to Matrix A benefits.
    She based this claim for additional compensation on a 2002 echocardiogram showing that
    she had valvular heart disease and did not have any of the listed alternative causation
    factors. The AHP Settlement Trust (the ―Trust‖), which administers the settlement fund,
    rejected her request for Matrix A benefits. It determined that Matrix B applied to her
    claims because four echocardiograms performed between 2007 and 2009 showed that she
    had developed mitral annular calcification—one of the listed alternative causation
    factors—prior to her surgery. The District Court affirmed the Trust‘s determination, and
    Haberman subsequently filed this appeal.3 Both the Trust and class counsel have filed
    briefs opposing her request for Matrix A benefits.
    The question raised on appeal is whether the Settlement Agreement imposes a
    time limitation on the medical evidence upon which the Trust may rely in determining
    whether a claimant has an alternative causation factor. It is undisputed that FDA Positive
    regurgitation, which determines whether a claimant is entitled to Matrix benefits at all,
    must be diagnosed by an echocardiogram performed between beginning diet drug use and
    the end of the screening period on January 4, 2003. What the parties dispute is whether
    newly created fund based on the review of their claims. Haberman was one of the class
    members covered by the amendment. She received a distribution of $122,687.57.
    3
    The District Court had diversity jurisdiction pursuant to 
    28 U.S.C. § 1332
    . We have
    jurisdiction over this timely filed appeal under 
    28 U.S.C. § 1291
    . ―We apply ‗plenary
    review to a district court‘s construction of settlement agreements,‘ but we review any
    underlying factual findings for clear error.‖ In re Diet Drugs Prod. Liab. Litig., 
    706 F.3d 217
    , 223 n.4 (3d Cir. 2013) (quoting Coltec Indus., Inc. v. Hobgood, 
    280 F.3d 262
    , 269
    (3d Cir. 2002)) (citing In re Cendant Corp. Prides Litig., 
    233 F.3d 188
    , 193 (3d Cir.
    2000)).
    4
    this same limitation applies to the diagnosis of alternative causation factors. Because the
    screening period ended on January 4, 2003, application of this limitation would preclude
    the Trust from relying on the echocardiograms performed between 2007 and 2009 to
    determine whether Haberman‘s claim should be resolved under Matrix A or Matrix B.
    Settlement agreements are interpreted according to ―basic contract principles.‖ In
    re Cendant Corp., 
    233 F.3d at 193
    . Under Pennsylvania law,4 when a term in an
    agreement is clear and unambiguous, its meaning ―must be determined from the four
    corners of the contract.‖ Glenn Distribs. Corp. v. Carlisle Plastics, Inc., 
    297 F.3d 294
    ,
    300 (3d Cir. 2002) (citing Steuart v. McChesney, 
    444 A.2d 659
    , 661 (Pa. 1982)). In
    contrast, ―if the written contract is ambiguous, a court may look to extrinsic evidence to
    resolve the ambiguity and determine the intent of the parties.‖ 
    Id.
     (citing Bohler-
    Uddeholm Am., Inc. v. Ellwood Grp., Inc., 
    247 F.3d 79
    , 93 (3d Cir. 2001)).
    We believe the Settlement Agreement is unambiguous in not placing a time limit
    on the medical evidence on which the Trust can base its determination of whether an
    alternative causation factor is present. The relevant provision of the Settlement
    Agreement states that Matrix B applies to ―Diet Drug Recipients who ingested [diet
    drugs] for sixty-one (61) or more days, who were diagnosed by a Qualified Physician as
    FDA Positive by an Echocardiogram performed between the commencement of Diet
    Drug use and the end of the Screening Period, with any of the following conditions.‖ J.A.
    4
    The parties do not address what jurisdiction‘s law is applicable. We have previously
    applied Pennsylvania law in interpreting the Diet Drugs settlement. See In re Diet
    Drugs., 706 F.3d at 223 n.5. We presume that Pennsylvania law applies here as well.
    5
    at 75–77 (emphasis added). It then lists a series of conditions, the alternative causation
    factors, among which is mitral annular calcification. Id. at 76.
    On its face, the provision refers to ―Diet Drug Recipients‖ who have ―any of the
    following conditions.‖ The commas separating ―who who were diagnosed by a Qualified
    Physician as FDA Positive by an Echocardiogram performed between the
    commencement of Diet Drug use and the end of the Screening Period‖ support this literal
    reading. In addition, some of the alternative causation factors contain their own
    timeframes that preclude them from being diagnosed by an echocardiogram performed
    between the outset of diet drug use and the end of the screening period. One of the
    factors listed, for example, is ―FDA Positive regurgitation (confirmed by
    Echocardiogram) prior to [diet drug] use for the valve that is the basis of the claim.‖ Id.
    at 77. This alternative causation factor must expressly be diagnosed before, not after, the
    beginning of diet drug use.5
    Haberman‘s argument that the temporal limitation does apply to the diagnosis of
    alternative causation factors primarily relies on the rule of the last antecedent. This ―rule
    generally holds ‗that qualifying words, phrases, and clauses are to be applied to the words
    or phrase immediately preceding and not to others more remote.‘‖ Stepnowski v. C.I.R.,
    
    456 F.3d 320
    , 324 (3d Cir. 2006) (quoting United States v. Hodge, 
    321 F.3d 429
    , 436 (3d
    Cir. 2003)). Applying this rule, Haberman argues that ―the phrase with any of the
    5
    Moreover, at least one other alternative causation factor—a ―[h]istory of daily use of
    methysergide or ergotamines for a continuous period of longer than 120 days‖—
    presumably cannot be diagnosed by an echocardiogram at all. 
    Id.
    6
    following conditions modifies the immediately preceding phrase who were diagnosed.‖
    Appellant‘s Br. at 26–27 (emphases in original).
    We do not agree that the last-antecedent rule requires us to adopt this reading of
    the provision. The rule of the last antecedent, despite its name, is a guide, not a binding
    rule of interpretation. Stepnowski, 
    456 F.3d at 324
    . As discussed, applying this
    limitation to the diagnosis of all alternative causation factors would be, among other
    things, at odds with the literal words as well as the timeframes that the Settlement
    Agreement provides for some of those factors.
    *   *   *   *   *
    To summarize, Haberman argues that the Settlement Agreement prohibits the
    Trust from relying on four echocardiograms conducted between 2007 and 2009 to
    determine whether she was entitled to Matrix A or Matrix B benefits. The Agreement,
    however, does not impose that limitation. Accordingly, we affirm the District Court‘s
    order denying her challenge to the Trust‘s determination that she is not entitled to Matrix
    A benefits.
    7