Lead Opinion
The opinion of the Court was delivered by
This products-liability case poses two troubling questions: (1) whether the Federal Cigarette Labeling and Advertising Act, 15 U.S.C. §§ 1331-41 (1982 & Supp. III 1985) (hereinafter Cigarette Act), preempts plaintiffs claims, and (2) whether the recently-enacted New Jersey Products Liability Law, N.J.S.A. 2A:58C-1 to -7 (hereinafter Products Liability Law) is applicable retroactively and renders a surviving claim invalid as a matter of law. The Law Division entered an order of partial summary judgment in faver of defendant Brown & Williamson Tobacco Co. Dewey v. R.J. Reynolds Tobacco Co., 216 N.J.Super. 347, 358,
I
In 1982 plaintiff, Claire Dewey, individually and as executrix of her husband’s estate, sued R.J. Reynolds Tobacco Co., R.J. Reynolds Industries, Inc., American Brands, Inc., and Brown & Williamson Tobacco Co. Plaintiff’s complaint alleged that her husband had developed lung cancer from smoking defendants’ cigarettes from 1942 until eight months before his death in 1980. Count one asserted general theories of design defect, including a claim of inadequate warning, and count two alleged theories of fraud and misrepresentation in advertising. Counts three and four were derivative.
During discovery, plaintiff disclosed that her husband had not smoked defendant Brown & Williamson’s cigarettes (“Viceroy”) until 1977, thirty-five years after he had started to smoke and eleven years after Congress had enacted the Cigarette Act, which requires that each package of cigarettes carry a warning of the alleged health hazards of smoking. See 15 U.S.C. § 1333. Brown & Williamson then moved for summary judgment on two grounds: (1) that the Cigarette Act preempted all of plaintiff’s claims, and, alternatively, (2) that the complaint was deficient as a matter of New Jersey substantive law because comment i of Section 402A of the Restatement of Torts (Second) (hereinafter Restatement) bars the imposition of strict liability for a product “whose danger is contemplated by the ordinary consumer who purchases it, with the ordinary knowledge common to the community as to its characteristics * * *.”
The trial court dismissed so much of the first count of plaintiff’s complaint as alleged liability for failure to warn, and the entire second count, which alleged fraud and misrepresentation in advertising, on the ground that the Cigarette Act preempts all those claims. 216 N.J.Super. at 355,
The trial court in this case, however, did not dismiss plaintiff’s design-defect claim on preemption grounds. The court believed that “Cipollone made clear that the regulatory scheme of the [Cigarette] Act and the federal interest involved was not so pervasive as to preclude all tort remedies which a plaintiff in smoking and health-related litigation may have under state law.” 216 N.J.Super. at 356, 523 A.2d 712. Plaintiff could pursue a design-defect claim by showing, under the “risk-utility” test for determining design defect, that the risks posed by cigarettes outweighed their utility. She did not have to prove the existence of an alternative, safer design. Ibid. The court made no mention of the impact of comment i of Restatement Section 402A on the claim that survived preemption.
The Appellate Division affirmed substantially for the reasons expressed by the trial court, subject to “such modifications as intervening law makes necessary,” 225 N.J.Super. at 377,
In addition to granting plaintiff and Brown & Williamson leave to appeal, we allowed defendant R.J. Reynolds Tobacco Company to file a brief and appear as intervenor.
II
Integral to our analysis is a preliminary determination of whether plaintiff’s complaint states a claim for design defect. Although our Rules of Court require that “all pleadings must be construed liberally in the interest of justice, R. 4:5-7, a party’s pleadings must nonetheless fairly apprise an adverse party of the claims and issues to be raised at trial.” Miltz v. Borroughs-Shelving, 203 N.J.Super. 451, 458,
Although the first count of the second amended complaint does not contain the words “design defect,” the complaint does allege that defendants’ tobacco products “were not reasonably fit, safe and suitable for human use at the time the products were placed in the stream of commerce” — the talismanic language of a strict-liability claim. See Suter v. San Angelo Foundry & Mach. Co., 81 N.J. 150, 176,
-A-
We turn to the issue of whether the federal Cigarette Act preempts any of plaintiffs common-law tort claims. Defendants contend that although the Appellate Division correctly affirmed the trial court’s dismissal of plaintiff’s inadequate-warning and fraudulent-advertising claims on preemption grounds, the court should also have held that the Cigarette Act preempts plaintiff’s alternative design-defect claim. Plaintiff counters that dismissal, on the basis of preemption, of any of the theories alleged in her complaint would represent a misapplication of United States Supreme Court precedent.
Pursuant to the Supremacy Clause of the United States Constitution, article VI, clause 2, Congress may preempt state common law as well as state statutory law through federal legislation. Chicago N.W. Transp. Co. v. Kalo Brick & Tile Co., 450 U.S. 311, 325-26, 101 S.Ct. 1124, 1134, 67 L.Ed.2d 258, 270 (1981). The essential question for any preemption analysis is “whether Congress intended that the federal regulation supersede state law.” Louisiana Pub. Serv. Comm’n v. Federal Communications Comm’n, 476 U.S. 355, 369, 106 S.Ct. 1890, 1899,
Obviously, then, preemption often hinges “on * * * question[s] of statutory construction and interpretation.” Palmer v. Liggett Group,
when adjudicating federal questions, the state courts form an integral part of the national structure and that:
In that capacity they occupy exactly the same position as the lower federal courts, which are coordinate, and not superior to them. There is no appeal from the state to the lower federal courts. Instead both are subject to the reviewing power of the Supreme Court, which furnishes the unifying principle. Decisions of a lower federal court are no more binding on a state court than they are on a federal court not beneath it in the judicial hierarchy. [Id. at 37,214 A.2d 393 (quoting Note, supra, 48 Colum.L.Rev. at 946-47).]
Neither Coleman nor the article quoted in Coleman distinguished between the binding effect of decisions involving constitutional interpretation and those involving statutory interpre
Instead, the operative principle that informs the discussion is the principle of “judicial comity.” Stated simply, lower-federal-court decisions in this area should be accorded due respect, particularly where they are in agreement. See, e.g., State v. Norflett, 67 N.J. 268, 286,
-B-
Perhaps the most significant event that precipitated the Cigarette Act was the 1964 Surgeon General’s Advisory Committee Report, which authoritatively concluded that “[c]igarette smoking is a health hazard of sufficient importance in the United States to warrant appropriate remedial action.” H.R.Rep. No. 449, 89th Cong., 1st Sess. 1, reprinted in 1965 “U.S.Code Cong. & Admin. News” 2350, 2351. Specifically, the report found that smoking was related to lung cancer, chronic bronchitis, emphysema, cardiovascular diseases, and cancer of the larynx. The report also concluded that “overwhelming evidence indicates that smoking — its beginning, habituation, and occasional discontinuation — is to a large extent psychologically and socially determined.” Id. at 2357. Public response to the report was “immediate and vocal.” Palmer v. Liggett Group, supra,
The Federal Trade Commission also responded to the Surgeon General’s Advisory Committee report by immediately issu
Among the significant provisions of the Cigarette Act is the statement of policy and purpose, which originally provided:
It is the policy of the Congress, and the purpose of this chapter, to establish a comprehensive Federal program to deal with cigarette labeling and advertising with respect to any relationship between smoking and health, whereby—
(1) The public may be adequately informed that cigarette smoking may be hazardous to health by inclusion of a warning to that effect on each package of cigarettes; and
(2) commerce and the national economy may be (A) protected to the maximum extent consistent with this declared policy and (B) not impeded by diverse, nonuniform, and confusing cigarette labeling and advertising regulations with respect to any relationship between smoking and health. [15 U.S.C. § 1331.]
Changes to subsection (1) made in 1984 are not relevant to this appeal.
Section 1333 of the Cigarette Act prescribes the exact language to be placed on the warning label. The label required in the original 1965 enactment was: “Warning: The Surgeon General Has Determined That Cigarette Smoking May Be Dangerous To Your Health.” 15 U.S.C. § 1333 (1965). That warning was subsequently strengthened in 1970 to read: “Warning: The Surgeon General Has Determined That Cigarette Smoking Is Dangerous To Your Health.” 15 U.S.C. § 1333 (1970). A 1984 revision to that section requires four rotating warnings that specifically describe the hazards attendant to smoking. 15 U.S.C. § 1333 (1984). Thus, the tentative message of the 1965 warning has been replaced by stronger assertions of the dangers of smoking.
Also relevant is the Cigarette Act’s preemption section, which provided originally that “no statement relating to smoking and health, other than the statements required by section 1333 of
(b) No requirement or prohibition based on smoking and health shall be imposed under State law with respect to the advertising or promotion of any cigarettes the packages of which are labeled in conformity with the provisions of this chapter.
-c-
Because we do not write on a clean slate, we briefly examine the slate as it comes to us, beginning with the Third Circuit’ decision in Cipollone v. Liggett Group, supra,
Consequently, the court examined the principles of implied preemption. As á preliminary matter, the court observed that although informative, the “vast” legislative history of the Cigarette Act was not “wholly dispositive of the issue.”
The Cipollone court then turned to the second form of implied preemption, termed “actual conflict,” which occurs when state law creates “an obstacle to the execution of the full purposes and objectives of Congress.” Id. at 187 (quoting Hines v. Davidowitz, supra, 312 U.S. at 67, 61 S.Ct. at 404, 85 L.Ed. at 587). According to the court, the Cigarette Act “represents a carefully drawn balance between the purposes of warning the public of the hazards of cigarette smoking and protecting the national economy.” Ibid. Allowing state-law damage claims to proceed would “upset” that balance by effectively requiring manufacturers to change their warning labels. Ibid. Consequently, the Court concluded that the Cigarette Act preempts “state law damage actions relating to smoking and health that challenge either the adequacy of the warning on cigarette packages or the propriety of a party’s actions with respect to the advertising and promotion of cigarettes.” Ibid. (footnote omitted). In addition, it found that the Act preempts all state-law damage claims that necessarily depend on a duty to provide an adequate warning. Ibid.
The Cipollone rationale found favor with four federal circuit courts: the first, Palmer v. Liggett Group, supra, 825 F.2d
It should be noted, however, that two of the federal circuit court opinions were reversals of lower-court decisions that had concluded that the Cigarette Act had no preemptive effect. See Palmer v. Liggett Group, 633 F.Supp. 1171 (D.Mass.1986), rev’d,
Specifically, the intermediate appellate court in Forster disagreed with the federal Circuit Courts’ approach to preemption, concluding that the traditional presumption against preemption is “heightened” by the following four factors: (1) the Cigarette Act does not explicitly preempt state tort claims, id. at 696; (2) the matter involves the state police powers of protecting the health and safety of the public, id. at 696-98; (3) the legislative history of the Cigarette Act, which the Third Circuit completely disregarded in Cipollone, indicates that Congress did not intend to supersede the traditionally state-run area of tort com
Like the trial-court decisions in Cipollone and Palmer, the Minnesota Court of Appeals decision in Forster was eventually reversed on appeal.
-D-
In deciding the preemption issue, we first point out that “the settled mandate” governing preemption of matters traditionally under state supervision “is not to decree such a federal displacement ‘unless it was the clear and manifest purpose of Congress.’ ” Florida Lime & Avocado Growers v. Paul, supra, 373 U.S. at 146, 83 S.Ct. at 1219,
The preemption arguments advanced by defendants are premised not on a clear showing of congressional intent but rather on dubious inferences and assertions. We agree with those courts that hold that the Cigarette Act neither expressly preempts common-law remedies nor impliedly preempts those remedies by pervasively occupying the field of law. Nor is there any indication that compliance with both state and federal law is impossible. See Pennington v. Vistron Corp., supra,
Preemption by “actual conflict,” as explained in Hines v. Davidowitz, supra, 312 U.S. 52, 61 S.Ct. 399, 85 L.Ed. 581, occurs in those instances in which, as a result of the operation of state law, “the purpose of the [federal] act cannot otherwise be accomplished — [] its operation within its chosen field else must be frustrated and its provisions be refused their natural effect * * *.” Id. at 68 n. 20, 61 S.Ct. at 404 n. 20, 85 L.Ed. at 587 n. 20. In contrast to express and implied preemption, the “actual conflict” analysis is “more an exercise of policy choices
The Cigarette Act’s statement of policy and purpose announces two separate goals: (1) “to adequately inform[] [the public] that cigarette smokipg may be hazardous to health by [the] inclusion of a warning to that effect on each package of cigarettes,” and (2) to protect “commerce and the national economy * * * to the maximum extent consistent with this declared policy [by] not impeding it with] diverse, nonuniform, and confusing cigarette labeling and advertising regulations.” 15 U.S.C. § 1331 (emphasis added). It is significant that the second goal, the protection of trade and commerce, must be achieved “consistent with” and not “to the detriment of” the first and principal goal — to inform the public adequately that cigarettes may be hazardous to health. H.R.Rep. No. 449, 89th Cong., 1st Sess. a, reprinted in “1965 U.S.Code Cong. & Admin.News” 2350 (noting that the Act’s “principal purpose” was to “provide adequate warning to the public of the potential hazards of cigarette smoking by requiring the labeling of cigarette packages with the [warning]”). Moreover, the secondary goal focuses on the need for uniform labeling and advertising regulations as a way of protecting commerce and the national economy, but does not go so far as to restrict the rights of injured consumers.
The question here is whether state common-law tort remedies will have the effect of creating “an obstacle to the accomplishment and execution of [those] purposes.” Hines, supra, 312 U.S. at 67, 61 S.Ct. at 404, 85 L.Ed. at 587. It is clear that the allowance of such remedies will further, not impair, the goal of
In other contexts the United States Supreme Court has commented on the regulatory effect of state damage actions. For example, in holding that the provisions in the National Labor Relations Act preempted a state common-law action for business losses associated with union picketing, the Court stated:
Our concern is with delimiting areas of conduct which must be free from state regulation if national policy is to be left unhampered. Such regulation can be as effectively exerted through an award of damages as through some form of preventative relief. The obligation to pay compensation can be, indeed is designed to be, a potent method of governing conduct and controlling policy
[San Diego Trades Council v. Garmon, 359 U.S. 236, 246-47, 79 S.Ct. 773, 780, 3 L.Ed.2d 775, 784 (1959).]
The quoted language has limited applicability, however, in view of the presumption in favor of federal preemption where the National Labor Relations Board (NLRB) is involved. Brown v. Hotel Employees, supra, 468 U.S. at 502, 104 S.Ct. at 3185,
More recently in Silkwood v. Kerr-McGee Corp., 464 U.S. 238, 104 S.Ct. 615,
It may be that the award of damages based on the state law of negligence or strict liability is regulatory in the sense that a nuclear plant will be threatened with damages liability if it does not conform to state standards, but that regulatory consequence was something that Congress was quite willing to accept. [Id. at 256, 104 S.Ct at 625,78 L.Ed.2d at 457 .]
Silkwood is relevant because it suggests that Congress may be willing to tolerate the regulatory consequences of the application of state tort law even where direct state regulation is preempted. See, e.g., Goodyear Atomic Corp. v. Miller, 486 U.S. 174, 186, 108 S.Ct. 1704, 1712, 100 L.Ed.2d 158, 171 (1988) (“Congress may reasonably determine that incidental regulatory pressure is acceptable, whereas direct regulatory authority is not”). And just this term, in English v. General Electric Co., — U.S. -, 110 S.Ct. 2270, 110 L.Ed.2d 65 (1990), the Court held that a nuclear-plant employee’s state-law claim for intentional infliction of emotional distress based on employer’s alleged retaliatory firing for plaintiff’s “whistleblowing” did not conflict with federal regulations or specific remedies of the Energy Reorganization Act, despite tangential effect on their purposes, and hence was not preempted by federal law. Both Silkwood and English, therefore, pose an obstacle to defendants’ “actual conflict” analysis, which is premised solely on the assertion that Congress could never have intended to tolerate such tension. See also Cipollone, supra,
Instead, in order to determine whether the goal of uniformity will be impaired, we prefer to scrutinize the actual extent to which state-law damage claims have a “regulatory effect”. Although liability may indirectly provide incentives to change behavior, the form of such change is never dictated by a court unless, of course, it be by way of injunctive or declaratory relief. Cipollone v. Liggett Group, supra, 593 F.Supp. at 1154; see also Garner, “Cigarette Dependency and Civil Liability: A Modest Proposal,” 53 S.Cal.L.Rev. 1423, 1454 (1980) (“a damages award * * * requires only payment — it is not an injunction requiring the defendant to incorporate into its advertising a fixed legend different from the federally required label”). In this case a manufacturer that incurs a judgment of liability may change its conduct by (1) adding an additional warning (which would not be barred under the Cigarette Act because the preemption section provides that no statement shall be “required,” hence, there is no prohibition against a manufacturer “voluntarily” saying more); or (2) placing a package insert in the product, as has been done with a multitude of products; or (3) simply choosing to do nothing and risking exposure to liability. “The decision * * * to choose whichever path is most prudent — is up to the industry. In either case, as long as it continues to meet the requirements of Federal law, it is free to meet its state-imposed obligations to its customers as it sees fit.” Tribe, “Federalism With Smoke and Mirrors,” The Nation, June 7, 1986, at 788. Defendants overstate the regulatory pressure that state-law damage claims would generate.
More significantly, defendants’ analysis completely ignores the fact that state-tort claims advance a substantial goal apart from regulating behavior: to provide compensation to those injured by deleterious products when that result is consistent
even if the ultimate purposes of federal and state law in this area are the same, a state (acting through its jurors) may assign distinct weight to the elements which go into determining whether a substance as labelled is of sufficient net benefit as to warrant its use. * * * [Thus] a state may choose to tip the scales more heavily in favor of the health of its citizens than EPA is permitted to by FIFRA. [736 F.2d at 1540.]
In rejecting Chevron’s contention that the exclusive “regulatory aim” of FIFRA would be frustrated by state damage actions, the court stated:
Damage actions typically, however, can have both regulatory and compensatory aims. Moreover, these aims can be distinct; it need not be the case, as Chevron apparently assumes, that the company can be held liable for failure to warn only if the company could actually have altered its warning. * * * In this case, a Maryland jury found that the EPA-approved label did not sufficiently guard against certain injuries. Even if Chevron could not alter the label, Maryland could decide that, as between a manufacturer and an injured party, the manufacturer ought to bear the cost of compensating for injuries that couldhave been prevented with a more detailed label than that approved by the EPA. That is, Maryland can be conceived of as having decided that, if it must abide by EPA’s determination that a label is adequate, Maryland will nonetheless require manufacturers to bear the risk of any injuries that could have been prevented had Maryland been allowed to require a more detailed label or had Chevron persuaded EPA that a more comprehensive label was needed. [Id. at 1541 (emphasis added).]
Similarly, in this case, a New Jersey jury could decide that a cigarette manufacturer, rather than an injured party, ought to bear the cost of injuries that could have been prevented with a more detailed warning label than that required under the Cigarette Act. Cf. Freund v. Cellofilm Properties, Inc., 87 N.J. 229, 238 n. 1,
Like cigarettes, paraquat has been “extensively regulated since 1966 by the federal government.” Ferebee v. Chevron Chem. Co., supra, 736 F.2d at 1532. The insecticide can be sold in the United States only when accompanied by a label approved by the EPA. Id. at 1539. Moreover, FIFRA contains a preemption section, which provides that a “State shall not impose or continue in effect any requirement for labeling * * * in addition to or different from those required under this subchapter.” 7 U.S.C. § 136v(b). No doubt such a provision was intended to promote a similar goal of uniformity.
The Ferebee case prompts an additional observation: defendants’ “implied preemption through incidental regulatory effect” analysis is equally applicable to the myriad of other federal labeling statutes and regulations that have as their foundation an express or implied goal of uniform labeling. The United States Food and Drug Administration (FDA), for example, prescribes warnings to be used on oral contraceptives to ensure that patients are “fully informed of the benefits and risks involved in the use of these drugs,” 43 Fed.Reg. 4220 (1978); 21 C.F.R. § 310.501(a) (1984), and requires “precise and nationally uniform” labeling in that respect. 21 C.F.R.
Another analogous statute is the Federal Hazardous Substances Act (FHSA), 15 U.S.C. § 1261 et seq., which requires that hazardous household substances sold in interstate commerce have a label containing specific warnings and instructions. 15 U.S.C. § 1261(p), 1262, 1263. That Act provides that states may not establish or continue “a requirement applicable to such substance * * * unless such requirement is identical to the warning established pursuant to the Act.” Pub.L. 94-284, § 17(a), 90 Stat. 510 (1976). Defendants’ argument suggests that compliance with the FHSA would preclude a finding of negligence for failure to give additional warnings. The FHSA, however, prescribes only the minimum warning. It does not immunize the manufacturer of a hazardous product from failure to supply an adequate warning. Burch v. Amsterdam Corp.,
Finally, defendants contend that the Cigarette Act preempts plaintiff’s design-defect claims because those claims would necessarily disturb the balance struck by Congress between its concern for the health of Americans and for the health of the tobacco industry. We find no legislative or judicial support for the proposition that Congress engaged in its own risk-utility analysis and decided that cigarettes were not defectively designed.
We are persuaded by the view most forcefully stated by Solicitor General Kenneth Starr, in his unpublished monograph “The Law of Preemption,” that “[o]ur federal system, with its
We hold that the Cigarette Act does not preempt plaintiff’s claims.
Ill
We focus now on the second issue on this appeal, namely, whether the New Jersey Products Liability Law, which in N.J.S.A. 2A:58C-3a(2) provides a defense to manufacturers and sellers for harms caused by products whose dangerous propensities are known to the ordinary user, can retroactively insulate these defendants from liability for design defects inherent in their cigarettes.
New Jersey’s tort-reform statute, which became effective after the trial court’s decision in this ease, was intended to “establish clear rules [in] actions for damages for harm caused by products, including certain principles under which liability is imposed and the standards and procedures for the award of punitive damages.” N.J.S.A. 2A:58C-1. The Products Liability Law was not intended to “codify all issues relating to product liability, but only to deal with matters that require clarification.” Ibid. The Products Liability Law leaves unchanged the three theories under which a manufacturer or seller may be held strictly liable for harm caused by a product — defective
The new statute, however, establishes new rules regarding the burden of proof and the imposition of liability. Those changes are not to be applied to products-liability actions instituted on or before the date of enactment, a category that includes this case. L.1987, c. 197, § 8. That provision reinforces the presumption in New Jersey favoring the prospective application of a statute, Gibbons v. Gibbons, 86 N.J. 515,
Section 3a(2) provides in part as follows:
a. In any product liability action against a manufacturer or seller for harm allegedly caused by a product that was designed in a defective manner, the manufacturer or seller shall not be liable if:
(2) The characteristics of the product are known to the ordinary consumer or user, and the harm was caused by an unsafe aspect of the product that is an inherent characteristic of the product and that would be recognized by the ordinary person who uses or consumes the product with the ordinary knowledge common to the class of persons for whom the product is intended, except that this paragraph shall not apply to industrial machinery or other equipment used in the workplace and is not intended to apply to dangers posed by products such as machinery or equipment that can feasibly be eliminated without impairing the usefulness of the product.
In O’Bren, the Supreme Court endorsed the use of risk-utility analysis since it “provides the flexibility necessary for an appropriate adjustment of the interests of manufacturers, consumers and the public.” 94 N.J. at 183, [463 A.2d 298 ]. Moreover, the O’Brien court made clear that in a design-defect case containing a claim that a product is unavoidably unsafe, manufacturers cannot insulate themselves from liability merely by placing warnings on their products. [216 N.J.Super. at 357,523 A.2d 712 .]
Hereafter, under the Products Liability Law, the consumer-expectations test cannot be avoided in a claim for design defect.
Section 3a(2) also modifies the method of analyzing “obvious danger” as established in Campos v. Firestone Tire & Rubber Co., supra, 98 N.J. 198,
Although some jurisdictions have adopted an “obvious danger rule” that would absolve a manufacturer of a duty to warn of dangers that are objectively apparent, in our state the obviousness of a danger, as distinguished from a plaintiff’s subjective knowledge of a danger, is merely one element to be factored into the analysis to determine whether a duty to warn exists. [Id. at 207,485 A.2d 305 .]
Instead of representing a single factor in the analysis, “obvious danger” has now been transformed into a defense, except in
Defendant’s argument that section 3a(2)’s adoption of Restatement Section 402A’s comment i represents a mere codification of New Jersey common law, and hence is entitled to retroactive application, likewise must fall. Comment i defines the term “unreasonably dangerous” by stating that
[mjany products cannot possibly be made entirely safe for all consumption, and any food or drug necessarily involves some risk or harm, if only from over-consumption. * * * That is not what is meant by “unreasonably dangerous” in this Section. The article sold must be dangerous to an extent beyond that which would be contemplated by the ordinary consumer who purchases it, mth the ordinary knowledge common to the community as to its characteristics. * * * Good tobacco is not unreasonably dangerous merely because the effects of smoking may be harmful; but tobacco containing something like marijuana may be unreasonably dangerous.
The “good tobacco” example included in comment i has never been adopted by this Court. Even though in Cepeda v. Cumberland Engineering Co., 76 N.J. 152, 170,
explains that the qualification “unreasonably dangerous” was meant to negate the notion that products normally useful, such as sugar, whiskey, tobacco, or butter, could be regarded as defective because, if used improperly, excessively or in an adulterated condition, they could also be harmful,
the Court never embraced that proposition as a statement of New Jersey law. See Suter, supra, 81 N.J. at 187,
that recovery in a products liability action should be permitted only if a product is more dangerous than that contemplated by the average consumer, [which would] permit the low esteem in which the public might hold a dangerous product to diminish the manufacturer’s responsibility for injuries caused by that product. [Barker v. Lull Eng’g Co., Inc., 20 Cal.3d 413, 425, 573 P.2d 443 , 451, 143 Cal.Rptr. 225, 233 (1978)]
Indeed, if any trend is apparent, it is this Court's reluctance to adhere to the restrictive language in comment i’s formulation of strict liability, which would of course include the “good tobacco” example.
As a last resort, defendants turn to the legislative history of the Products Liability Law to support its assertion that comment i in its entirety has been embraced by this Court. The Assembly Insurance Committee Statement to Senate, No. 2805, explains that
certain provisions of the act simply codify the existing common law of the State, which should continue to apply in pending cases as well as new cases. For example, section 2 states that the burden is on the claimant in a product liability action to prove by a preponderance of the evidence that the product is defective. This is the rule under the existing common law. Similarly, the New Jersey courts have adopted certain provisions of the commentary to the American Law Institute’s "Restatement (Second.) of Torts, ” (e.g., comments i and k to section 402A) that are codified in this act. (Emphasis added.)
Defendants add that even if the Assembly Insurance Committee was incorrect in its assessment of the common law, its statement must be construed as evidence of the legislature’s intent that section 3a(2) apply to pending cases — an argument that the federal district court in Cipollone found persuasive, despite that court’s conclusion that N.J.S.A. 2A:58C-3a(2) did not codify existing common law. See Cipollone v. Liggett Group, supra,
Putting aside the legislature’s interpretation of common law, the Assembly Insurance Committee Statement is not inconsistent with our position. Citing comment i as an example, it asserts that certain provisions in the Restatement’s commentary were adopted prior to the Products Liability Law. As previously discussed, in Suter, supra, 81 N.J. at 171, 406 A.2d 140, this Court did adopt comment i to the extent that it
Having concluded that section 3a(2) of the Products Liability Law does not codify existing common law, and hence is inapplicable, we are left with the remaining argument that as a matter of public policy this Court should immunize cigarette manufacturers from liability for the harm caused by their products by finding that no duty exists. See, e.g., Cepeda v. Cumberland Eng’g Co., supra, 76 N.J. at 173,
Defendants’ argument completely ignores the extensive efforts of the tobacco manufacturers to saturate the public with information regarding the benefits of cigarette smoking, the aim of which is to rebut the assertions of public-health advocates and the Surgeon General. We note that in the ensuing quarter-century since the 1964 Surgeon General’s Advisory
In sum, our decision today alters the Appellate Division decision by overturning the dismissal of plaintiff’s failure-to-warn and misrepresentation claims, because we conclude that the Cigarette Act does not preempt such claims. We agree, however, with the Appellate Division’s refusal to apply the “comment i” example relating to tobacco and with its decision to allow plaintiff’s design-defect claim to proceed under the risk-utility analysis. ' We therefore refuse to apply N.J.S.A. 2A:58C-3a(2) retroactively to eliminate plaintiff’s design-defect claim.
Judgment affirmed in part, reversed in part. We remand the cause to the Law Division.
Concurrence Opinion
concurring in part, dissenting in part.
I respectfully dissent from the conclusion that the labeling requirement of the Federal Cigarette Labeling and Advertising
The majority correctly states that in the interpretation of federal statutes principles of comity dictate that lower federal court decisions “be accorded due respect, particularly where they are in agreement, [citation omitted]. Judicial comity helps to ensure uniformity and hence discourages forum shopping.” From this posture the Court then undertakes its “independent analysis of the federal scheme,” an inquiry in which it rejects the well-reasoned, unanimous determinations of the five federal Circuit Courts of Appeal and the Supreme Court of Minnesota which all conclude that Congress has preempted the question of adequate warnings concerning the use of cigarettes. So much for comity.
The Act’s twofold concern is to inform the public of the health hazards posed by cigarette smoking without exposing “commerce and the national economy” to the confounding effects of “diverse, nonuniform, and confusing cigarette labeling and advertising regulations with respect to any relationship between smoking and health.” 15 U.S.C.A. § 1331. Accordingly, at the time relevant to this case the Act mandated that this be accomplished by requiring that the following statement conspicuously appear on each package of cigarettes: “Warning: The Surgeon General Has Determined That Cigarette Smoking is Dangerous to Your Health.” 15 U.S.C.A. § 1333.
15 U.S.C.A. § 1334 is entitled “Preemption.” It provides
(a) No statement relating to smoking and health, other than the statement required by Section 1333 of this title, shall be required on any cigarette package.
(b) No requirement or prohibition based on smoking and health shall be imposed under State law with respect to the advertising or promotion of any cigarettes the packages of which are labeled in conformity with the provisions of this chapter.
The structure of the majority’s holding merits close attention. It rests on the premise that the Act permits the states to compromise the federal goal of protecting commerce and the national economy in order to further inform the public about the hazards of smoking. Its rationale is that the protection of trade and commerce is a “secondary goal” because it “must be achieved ‘consistent with’ and not ‘to the detriment of’ the first and principal goal.” Therefore, allowing challenges to the adequacy of warnings in state court proceedings does not conflict with the federal statute since its “principal goal” of adequately warning the public will be thereby better served.
As to the “secondary goal” of immunizing the cigarette industry from state regulation, the Court reasons that the impact of adverse jury verdicts based upon inadequate warnings constitutes only incidental regulatory pressure. Because “incidental regulatory pressure is acceptable, whereas direct regulatory authority [such as an injunction or declaratory relief] is not,” the Act’s prohibition against further regulation is not breached by challenges to the adequacy of warnings in state court product liability actions. The cigarette manufacturer, states the majority, is free to decide how it shall respond to such liability verdicts, that is, whether to modify the warnings or simply ignore the import of the verdicts.
The other justification given for diminishing the protection Congress accorded commerce and the national economy is that
It can be seen that the Court’s holding is vitally dependent upon its assumptions that under the Act one goal is subordinate to the other and that state courts may improve upon the warning statements required by Congress at the expense of commerce and the national economy. This is not what the Act says.
In limiting its attention to the statutory condition expressed in 15 U.S.C.A. § 1331 that protection of commerce and the national economy be “consistent with” the policy of adequate warnings, the Court overlooks the larger context of the declared congressional policy. 15 U.S.C.A. § 1331 states that policy “and the purpose of this chapter” to be the establishment of “a comprehensive Federal program to deal with cigarette labeling ... whereby” the public may be adequately informed and commerce may be protected. The word “whereby,” relates to “Federal program.” Thus, the Act itself creates the very “program ... whereby” commerce is given protection “to the maximum extent consistent with” warning the public. It not only sets forth the dual policy in the abstract, but also the bright-line warning language which forms the literal mechanics of its implementation. The preemption declaration of 15 U.S.C.A. § 1334 tells us that Congress wrote the language of the labeling requirement into 15 U.S.C.A. § 1333 to express its exclusive judgment as to how the competing values should be balanced. The Act leaves no doubt as to what warning should be given and how great an intrusion must be tolerated by commerce. Implicit in this is the conclusion that any attempted modification of that balance “under State law” would be in actual conflict with federal law. This is precisely the point of the federal circuit court decisions and the decision of the Supreme Court of Minnesota in Forster v. R.J. Reynolds Tobacco Co., 437 N.W.2d 655 (1989), in applying the Act’s preemption provision.
“a hard-fought, bitterly partisan battle in striking the compromise that became the Act. It is inconceivable that Congress intended to have that carefully wrought balance of national interests superseded by the views of a single state, indeed, perhaps of a single jury in a single state.
It was there held “that a suit for damages on a common law theory of inadequate warning — if the warning given complies with the Act — disrupts excessively the balance of purpose set by Congress, and is thus preempted.” Ibid. As the Supreme Court of Minnesota reasoned in Forster, supra,
The best indication of congressional intent, we think, is what Congress said in the statute’. Congress said it wanted to avoid diverse, nonuniform, and confusing regulations. This statement of intent is at odds with plaintiffs’ claim that Congress contemplated a diversity of conflicting state regulations coexisting with the federal regulatory scheme, or that Congress intended its warning to be a minimal warning to which a state could add further requirements. [Forster,437 N.W.2d at 660 ] [Footnote omitted]
See also Cipollone v. Liggett Group, Inc., 789 F.2d 181, 186 (3d Cir.1986) (“Even more important, we find the language of the statute itself a sufficiently clear expression of congressional intent without resort to the Act’s legislative history.”)
The majority states that the Act’s “secondary” goal of protecting commerce “focuses on the need for uniform labeling and advertising regulations as a way of protecting commerce and the national economy, but does not go so far as to restrict the rights of injured consumers in achieving that goal.” The emphasis on “regulations” is presumably used to suggest that the preemption provision is addressed solely to formal regulations promulgated by state administrative or legislative authority.
Moreover, claims of inadequate warning asserted in state court liability actions are pernicious in a sense not shared by governmental regulations. They are asserted after the fact, when compliance by the manufacturer is no longer possible to avoid the consequences of a particular suit. Regulations promulgated by state authority, once complied with, impose no duty on a manufacturer to respond in compensatory or punitive damages.
It is obvious that the congressional intent could not have been limited to protecting the industry from state regulatory action while leaving it open to the indirect regulation implicit in product liability suits based on claims of inadequate warning. Both have the proscribed regulatory effect. San Diego Bldg. Trades Council v. Garmon, 359 U.S. 236, 246-247, 79 S.Ct. 773, 780,
Applying this principle [that State law damage claims have a regulatory effect], we conclude that claims relating to smoking and health that result in liabilityfor noncompliance with warning, advertisement, and promotion obligations other than those prescribed in the Act have the effect of tipping the Act’s balance of purposes and therefore actually conflict with the Act.
See also Roysdon v. R.J. Reynolds Tobacco Co., 849 F.2d 230, 234 (6th Cir.1988).
Furthermore, I can make no sense of a federal statute which would preclude state legislatures from requiring further minimal warnings, but allow private litigants to run riot with claims of inadequate warnings — claims which might never have come into existence if local lawmakers had been permitted to act in the first place. Had Congress intended to permit litigants to assert these claims on a case-by-case basis there would be no reason to prohibit state legislatures from requiring warnings, in addition to those specified by the Act, to protect consumers from the very injury for which they later sue.
Cases cited by the majority lend no support to its judgment that the Cigarette Labeling Act does not preempt product liability suits based on inadequate warning. In Silkwood v. Kerr-McGee Corp., 464 U.S. 238, 104 S.Ct. 615, 78 L.Ed.2d 443 (1984), the Supreme Court decided in a five-four decision that a claim for punitive damages in an action for injuries resulting from the escape of nuclear radiation was not preempted by the Federal Atomic Energy Act of 1954, 42 U.S.C.A. § 2011 et seq. The case is distinguishable. First, unlike the Act herein, the Atomic Energy Act contained no preemption provision whatever. Palmer v. Liggett Group, Inc.,
Finally, in Silkwood the Supreme Court specifically found a clear congressional intent that state court tort remedies should remain available to those injured by nuclear incidents. Having
While it is true, as the majority states, that MacDonald v. Ortho Pharmaceutical Corp., 394 Mass. 131, 475 N.E.2d 65 (1985), cert. den. 474 U.S. 920, 106 S.Ct. 250, 88 L.Ed.2d 258 (1985), decided that compliance with FDA labels on oral contraceptives does not shield manufacturers from liability, it appears that the label requirements in that case merely took the form of a regulation promulgated by the FDA Commissioner who “specifically noted that the boundaries of civil tort liability for failure to warn are controlled by applicable State law.” Id.
In Ferebee v. Chevron Chemical Co.,
Finally, in Burch v. Amsterdam Corp.,
In my opinion, by allowing challenges to the adequacy of warnings on cigarette labels the Court is licensing a form of legal sanction forbidden by Congress. The federal legislation gives effect to the coordinate goals of protecting the public with minimal consequences to the cigarette industry. It does this by requiring that consumers be informed that cigarette smoking is “dangerous to your health,” reflecting a judgment that this was all an ordinary consumer need know to appreciate the risk of smoking and drawing the line at which personal responsibility begins. Implicit in this choice of words is a recognition that the extent to which the warning can be particularized is infinite and that there are few cases of which it can be said that the manufacturer adequately covered the myriad risk possibilities about which a consumer could claim a warning should have been, but was not, given. Although Congress intended to put the matter to rest, the decision of the majority
For affirmance in part; for reversal in part; for remandment — Justices CLIFFORD, HANDLER, O’HERN and STEIN, and Judges KING and COLEMAN — 6.
Concurring in part; dissenting in part — Judge ANTELL — 1.
Notes
A choice "akin to the free choice of coming up for air after being under water.” Palmer v. Liggett Group Inc., 825 F.2d 620, 627 (1st Cir.1987). The argument was there described as having been "disingenuously” maintained. Ibid.
Although the word "regulations" is used in the Act’s Declaration of Policy, 15 U.S.C.A. § 1331, the prohibition contained in 15 U.S.C.A. § 1334 is actually more broadly stated to extend to any requirements and statements relating to smoking and health "other than the statement required by section 1333 of this title." It should be noted that the preemption provision of § 1334(b) prohibits
It is not amiss to note that offensive collateral estoppel has been applied in product liability cases to preclude a producer from denying the inadequacy of a warning found inadequate in a previous case in which the producer defended the claim against a different plaintiff. Ezagui v. Don Chemical Corp., 598 F.2d 727 (2d Cir.1979); Fraley v. American Cyanimid Co., 570 F.Supp. 497 (D.Colo.1983). Although in Kortenhaus v. Eli Lilly & Co., 228 N.J.Super. 162, 549 A.2d 437 (1982), the Appellate Division concluded that collateral estoppel would be unfair under the facts presented, its potential applicability in a failure to warn case was recognized. For general contours of the doctrine, see Restatement, Judgments 2d § 29 at 291 (1982). Its conceivable implication to a cigarette producer is that once its warning is found inadequate, it could be barred from re-litigating the issue in later suits brought by other consumers. Thus, dissolution of the “maximum" protection to which it is entitled would be complete, and the purpose of the federal program, as to that producer, would be nullified.
