Opinion
In two published decisions the United States District Court for the Central District of California denied class certification in putative class actions brought by current and former users of the prescription drug Paxil against GlaxoSmithKline, Inc. (GSK), the drug’s manufacturer, which alleged GSK had deceptively advertised Paxil as non-habit-forming.
FACTUAL AND PROCEDURAL BACKGROUND
1. Johnson’s First Amended Complaint
Paxil, a drug manufactured and distributed by GSK, is prescribed for conditions including depression, panic disorder and generalized anxiety disorder. On January 14, 2003 Johnson filed his original complaint and on July 15, 2003 filed a first amended putative class action complaint against GSK on behalf of all California residents who had taken Paxil after 1992 and had become addicted to it or had suffered withdrawal symptoms when they attempted to stop taking it. 1 The complaint asserted causes of action for negligent misrepresentation, concealment, negligence, strict product liability and violation of California’s unfair competition law (Bus. & Prof. Code, § 17200 et seq. (section 17200)), largely on the basis GSK had falsely and deceptively advertised Paxil as non-habit-forming.
Johnson alleged he was prescribed Paxil in early 2000 for moderate anxiety caused by the stress of work and family. Johnson further alleged, albeit without specifying the timing, that he had seen television and heard radio advertisements stating Paxil had few side effects and was not addictive; in addition, his doctor never informed him of any side effects or addiction-related symptoms. For a short while the drug was effective; Johnson felt euphoric and better able to deal with stress. Johnson, however, began suffering from fatigue and sexual dysfunction, motivating him to discontinue using Paxil in January 2002. When Johnson stopped, he experienced severe physical and emotional withdrawal symptoms, including headaches, heart palpitations and the sensation of electric shocks throughout his body. Even after one year Johnson continued to suffer from, among other symptoms, insomnia and the electric shock sensation. Johnson alleged he would not have taken Paxil had these symptoms been explained to him by his doctor, who himself was inadequately warned by GSK about these symptoms.
The first amended complaint defined the putative class as “all California residents, who are not deceased, who have been prescribed, and have taken Paxil at any time after 1992, and who have suffered or continue to suffer from withdrawal episodes or symptoms, or those who have become addicted and/or [are] unable to stop taking Paxil for fear of these symptoms.” In response to the trial court’s request at a status conference for a definite class definition, in a joint statement filed June 25, 2004, the class definition was revised to include “all California residents, who are not deceased, who have been prescribed, and have taken Paxil at any time after 1992 until the present.”
3. GSK’s Motion for Summary Adjudication
On January 19, 2007 GSK filed a motion for summary adjudication to preclude Johnson’s lawsuit from proceeding as a class action. GSK asserted under the collateral estoppel principles applied to class action determinations by Division Four of this court in its then-recent decision in
Alvarez, supra,
a. Paxil I
On August 1, 2002 in
Paxil I, supra,
The district court denied the plaintiffs’ motion, generally finding they had failed “to define a manageable class” and had “failed to demonstrate that a manageable trial plan exist[ed] that would make a class action lawsuit feasible.”
(Paxil I, supra,
b. Paxil II
On March 24, 2003 the plaintiffs filed a second motion for class certification proposing only two classes. The equitable relief class consisted of California residents who took prescribed Paxil after December 29, 1992, and sought injunctive relief prohibiting certain GSK advertising statements and restitution pursuant to section 17200.
(Paxil II, supra,
Notwithstanding the court’s negative description of the classwide claims, however, accepting the plaintiff’s representations concerning the breadth of section 17200 (prior to its amendment by Proposition 64), the district court held “[t]here is no serious dispute that the proposed Equitable Relief Class meets Rule 23(a)’s numerosity and commonality requirements.”
(Paxil II, supra,
c. Alvarez v. May Dept. Stores Co.
In what appears to have been a case of first impression in California, the court in
Alvarez, supra,
The
Alvarez
court held the
Duran
and
Alvarez
complaints each alleged the same general misconduct concerning the same policies and procedures, occurring over approximately the same period of time. The same putative class of present and former employees was alleged in both cases; and the
Alvarez
plaintiffs conceded they were, by definition, included within the putative
Duran
class.
(Alvarez, supra,
4. The Trial Court’s Order Granting Summary Adjudication in Favor of GSK on the Class Issues
The trial court granted GSK’s motion on March 29, 2007, ruling the district court’s denials of class certification in
Paxil I
and
Paxil II
collaterally estopped Johnson from proceeding with a class action. The trial court stated, “The
In re Paxil
court twice considered and rejected a class identical to the one [Johnson] seeks.
Alvarez
and principles of collateral estoppel bar [Johnson] from again pursuing certification.” Johnson filed a timely notice of appeal. (See
Morrissey
v.
City and County of San Francisco
(1977)
1. Standard of Review
The trial court’s application of the doctrine of collateral estoppel or issue preclusion is a question of law subject to de novo review.
(Noble v. Draper
(2008)
2. The Doctrine of Collateral Estoppel (Issue Preclusion) and Class Action Determinations
a. Collateral estoppel generally
“ ‘Res judicata’ describes the preclusive effect of a final judgment on the merits. Res judicata, or claim preclusion, prevents relitigation of the same cause of action in a second suit between the same parties or parties in privity with them. Collateral estoppel, or issue preclusion, ‘precludes relitigation of issues argued and decided in prior proceedings.’ ”
(Mycogen Corp.
v.
Monsanto Co.
(2002)
A prior decision precludes relitigation of an issue under the doctrine of collateral estoppel only if five threshold requirements are satisfied: “First,
Even if all these requirements are satisfied, however, a court must analyze the public policies underlying the doctrine before concluding that collateral estoppel should be applied in a particular case.
(Pacific Lumber Co. v. State Water Resources Control Bd., supra,
37 Cal.4th at pp. 943-944;
Lucido v. Superior Court, supra,
51 Cal.3d at pp. 342-343.) “[I]n deciding whether to apply collateral estoppel, the court must balance the rights of the party to be estopped against the need for applying collateral estoppel in the particular case, in order to promote judicial economy by minimizing repetitive litigation, to prevent inconsistent judgments which undermine the integrity of the judicial system, or to protect against vexatious litigation.”
(Clemmer v. Hartford Ins. Co.
(1978)
b. Requirements for class certification
Class actions are statutorily authorized “when the question is one of a common or general interest, of many persons, or when the parties are numerous, and it is impracticable to bring them all before the court . . . .” (Code Civ. Proc., § 382.) “The party seeking certification has the burden to establish the existence of both an ascertainable class and a well-defined
“ ‘The adequacy inquiry . . . serves to uncover conflicts of interest between named parties and the class they seek to represent.’ [Citation.] ‘. . . To assure “adequate” representation, the class representative’s personal claim must not be inconsistent with the claims of other members of the class.’ ”
(J. P. Morgan & Co., Inc.
v.
Superior Court
(2003)
“A class action also must be the superior means of resolving the litigation, for both the parties and the court. [Citation.] ‘Generally, a class suit is appropriate “when numerous parties suffer injury of insufficient size to warrant individual action and when denial of class relief would result in unjust advantage to the wrongdoer.” [Citations.]’ [Citation.] ‘[Relevant considerations include the probability that each class member will come forward ultimately to prove his or her separate claim to a portion of the total recovery and whether the class approach would actually serve to deter and redress alleged wrongdoing.’ [Citation.] ‘[B]ecause group action also has the potential to create injustice, trial courts are required to “ ‘carefully weigh respective benefits and burdens and to allow maintenance of the class action only where substantial benefits accrue both to litigants and the courts.’ ” ’ ”
c. Principles of collateral estoppel apply to relitigation of class action determinations
If all five elements required for application of collateral estoppel are present, the doctrine is fully applicable to preclude relitigation of issues finally resolved as part of a class certification determination in a prior proceeding. (See
Alvarez, supra,
3. The Trial Court Erred in Ruling Collateral Estoppel Precluded Johnson’s Efforts to Pursue His Section 17200 Paxil Claim As a Class Action
a. The issue of adequacy of representation actually litigated and determined in Paxil II is not identical to the adequacy or typicality issues presented by Johnson’s putative class claim
The propriety of class certification was actually and necessarily litigated in
Paxil I, supra,
“Being a matter of
issue
preclusion, collateral estoppel is naturally confined to issues ‘actually litigated.’ [Citations.] [][] A corollary is that the issue decided previously be ‘identical’ with the one sought to be precluded. [Citations.] [][] Accordingly, where the previous decision rests on a ‘different factual and legal foundation’ than the issue sought to be adjudicated in the case at bar, collateral estoppel effect should be denied.”
(Wimsatt v. Beverly Hills Weight etc. Internat., Inc.
(1995)
Both
Paxil I
and
Paxil II
were litigated before the voters approved Proposition 64 on November 2, 2004 (effective the following day), which significantly restricted the previously broad standing requirements for pursuing a private cause of action under section 17200. Prior to their amendment by Proposition 64, section 17200 and related provisions permitted any person acting for the general public to sue for relief from unfair competition and did not predicate standing on a showing of injury or damage. (See
Californians for Disability Rights
v.
Mervyn’s, LLC
(2006)
The district court “assume[d] for the purposes of the class certification that Section 17200 ha[d] the broad scope that Plaintiffs ascribe[d] to it.”
(Paxil II, supra,
b. The primary rights theory does not permit application of collateral estoppel absent an identity of issues actually and necessarily litigated and finally decided on the merits
In
Alvarez, supra,
Relying on Alvarez, GSK argues the primary right asserted in Paxil I and Paxil II, on the one hand, and the case at bar, on the other hand, is the same—the right to litigate claims involving Paxil in a class action lawsuit— and that the differences in the issues actually litigated discussed in the preceding section of this opinion are immaterial to the application of collateral estoppel. The trial court, as well, quoted the Alvarez court’s language regarding primary rights in rejecting Johnson’s argument that identity of issues does not exist because rule 23, which governed the class determinations in Paxil II, purportedly differs from Code of Civil Procedure section 382.
Moreover, the procedural right to prosecute a claim as a class action, “a means to enforce substantive law” by collectively litigating substantive claims
(Washington Mutual Bank v. Superior Court
(2001)
4. Conclusion
To avoid possible uncertainty as to the reach of our reversal of the trial court’s order granting GSK’s motion for summary adjudication, we emphasize we are not deciding Johnson has established the existence of both an ascertainable class and a well-defined community of interest among class members. (See
Lockheed Martin Corp. v. Superior Court
(2003)
DISPOSITION
The order granting summary judgment on the class certification issues is reversed. Johnson is to recover his costs on appeal.
Woods, J., and Zelon, J., concurred.
A petition for a rehearing was denied October 14, 2008, and the opinion was modified to read as printed above. Respondent’s petition for review by the Supreme Court was filed December 23, 2008, S167892. Werdegar, J., and Corrigan, J., did not participate therein.
Notes
Other named plaintiffs were George Grair and Lynn Booker. For reasons unrelated to class certification, the trial court dismissed with prejudice all of Booker’s claims on June 2, 2005 and Grair’s claims on May 24, 2006.
The decision in
Alvarez, supra,
The other proposed class was a general causation issues class comprised of 215 California residents who had experienced one or more specified symptoms and would litigate the capacity of Paxil to cause the complained-of symptoms.
(Paxil II, supra,
218 F.R.D. at pp. 244, 248.)
The district court also found it “problematic” whether the named representatives’ claims were typical of those in the class.
(Paxil II, supra,
As the Supreme Court noted in
Mycogen Corp.
v.
Monsanto Co., supra,
28 Cal.4th at pages 896 to 897, footnote 7, traditionally the doctrine of res judicata defines the preclusive effect of a judgment in a prior proceeding in terms of both claim preclusion (at common law, merger and bar) and issue preclusion (collateral estoppel). (See, e.g.,
Brinton v. Bankers Pension Services, Inc.
(1999)
California courts properly give preclusive effect to final decisions by federal courts. (See
Younger v. Jensen
(1980)
“Rule 23(a) states four threshold requirements applicable to all class actions: (1) numerosity (a ‘class [so large] that joinder of all members is impracticable’); (2) commonality (‘questions of law or fact common to the class’); (3) typicality (named parties’ claims or defenses ‘are typical ... of the class’); and (4) adequacy of representation (representatives ‘will fairly and adequately protect the interests of the class’).”
(Amchem Products, Inc.
v.
Windsor
(1997)
As a general principle of due process of law, “one is not bound by a judgment
in personam
in a litigation in which he is not designated as a party or to which he has not been made a party by service of process.”
(Hansberry v. Lee
(1940)
In
Clemmer v. Hartford Insurance Co., supra,
As discussed, the court in
Alvarez v. May Dept. Stores Co., supra,
As Johnson contends, the
Alvarez
court’s emphasis on the absence of any challenge to the adequacy of the representation by the named plaintiffs in the earlier
Duran
case raises the question whether the denial of class certification may be enforced against an absent putative class member when, as here, the basis for the earlier determination was that the named representatives could not adequately represent the putative class. (See also
In re Bridgestone/Firestone, Inc., Tires Products, supra,
Additional questions regarding the
Alvarez
court’s virtual representation analysis are potentially raised by the United States Supreme Court’s recent decision in
Taylor v. Sturgell, supra,
The protections for absent class members prescribed by rule 23, of course, are afforded after a motion for class certification has been granted, not by the filing of a motion for certification that is denied. Similarly, the concept of a “properly conducted class action” suggests a class action that has been certified, following a hearing in which the named representatives have established they satisfy the requirements of rule 23, and then litigated to judgment or settled, not a individual lawsuit in which a motion for class certification was denied. Literally (and narrowly) read, therefore,
Taylor v. Sturgell, supra,
In its petition for rehearing, which we have denied, GSK correctly notes the court may refer to the entire record, as well as other extrinsic evidence, not simply the first court’s written decision, to determine what issues were actually and necessarily decided in the earlier case. (See generally 7 Witkin, California Procedure (5th ed. 2008) Judgment, § 417(1), p. 1062 [entire record in the first action may be admitted for the purpose of determining what issue was decided by the judgment].) However, when, as here, the first court expressly defines the issue it is deciding, we are not permitted to examine the record of the earlier proceeding and preclude litigation of issues that were raised and either could or should have been addressed in the first proceeding, but were not.
Proposition 64 also amended Business and Professions Code section 17203 to provide that, other than public officials, a person may pursue representative claims or claims on behalf of others only if the representative plaintiff complies with Code of Civil Procedure section 382, governing class actions.
In its ruling granting GSK’s motion for summary adjudication, the trial court stated, “[T]he In re Paxil court’s adequacy determination was not premised on any particular characteristic of the named plaintiffs, but on the potential conflicts of interest inherent in any class certified under the plaintiffs’ broad formulation of a § 17200 class.” To the extent the trial court understood Paxil II, supra, 218 F.R.D. at pages 246 to 247 as determining no putative class representatives could represent the class proposed, including potential plaintiffs who had seen or heard the allegedly deceptive, non-habit-forming advertisements prior either to taking or attempting to stop using Paxil, and who thereafter suffered serious withdrawal symptoms, we believe it simply misread Judge Pfaelzer’s decision.
As noted, the court also questioned whether the putative class representatives’ claims were “typical” of those in the class, once again based on the likelihood individuals who had never seen or heard the challenged advertisements and who, in fact, may not have suffered any adverse effects from having taken Paxil sought to represent a diverse class of Paxil users.
(Paxil II, supra,
Section 17200 defines “unfair competition” broadly to include “any unlawful, unfair or fraudulent business act or practice and unfair, deceptive, untrue or misleading advertising and any act prohibited by [California’s false advertising law (Bus. & Prof. Code, § 17500 et seq.)].”
Relying on material submitted by GSK in this proceeding, the trial court observed that one of the named class representatives in
Paxil II, supra,
The California Supreme Court is currently considering whether each member of a proposed class, or only the class representative, must have suffered “injury in fact” in a class action under section 17200 and whether each member of a proposed class must have relied on the manufacturer’s representation in order to bring a class action based on alleged misrepresentation of a product. (In re Tobacco II Cases, review granted Nov. 1, 2006, S147345 ; Pfizer, Inc. v. Superior Court, review granted Nov. 1, 2006, S145775; McAdams v. Monier, Inc., review granted Sept. 19, 2007, S154088.)
Noting an injury-in-fact standing requirement based on Article HI of the United States Constitution was applied by federal courts to plaintiffs asserting section 17200 claims prior to adoption of Proposition 64 (see, e.g.,
Lee v. American Nat’l Ins. Co.
(9th Cir. 2001)
The two cases cited by the
Alvarez
court in its discussion of the primary rights theory and collateral
estoppel—Balasubramanian v. San Diego Community College Dist.
(2000)
