In re "Agent Orange" Product Liability Litigation

635 F.2d 987, 1980 U.S. App. LEXIS 11998
CourtCourt of Appeals for the Second Circuit
DecidedNovember 24, 1980
DocketNo. 1069, Docket 80-7079
StatusPublished
Cited by73 cases

This text of 635 F.2d 987 (In re "Agent Orange" Product Liability Litigation) is published on Counsel Stack Legal Research, covering Court of Appeals for the Second Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re "Agent Orange" Product Liability Litigation, 635 F.2d 987, 1980 U.S. App. LEXIS 11998 (2d Cir. 1980).

Opinions

KEARSE, Circuit Judge:

This appeal presents the question whether claims asserted by veterans of the United States armed forces against companies which supplied the United States government with chemicals that are alleged to have been contaminated and to have injured the veterans and their families, are governed by federal common law. Defendants-appellants Diamond Shamrock Corporation, Monsanto Company, Thompson Hayward Chemical Company, Hercules Incorporated and the Dow Chemical Company were the manufacturers of various herbicides including “Agent Orange” (hereinafter collectively referred to as “Agent Orange”) for use by the military as defoliants in the Vietnam War. The plaintiffs, veterans of that war and their families, allege that they have sustained various physical injuries by reason of the veterans’ exposure to Agent Orange. Plaintiffs seek redress of those injuries under federal common law, and have invoked the “federal question” jurisdiction of the district court. 28 U.S.C. § 1331(a) (1976). Defendants contest the existence of a federal common law cause of action, and moved below to dismiss for lack of subject matter jurisdiction. The United States District Court for the Eastern District of New York, George C. Pratt, Judge, denied their motion. Defendants obtained certification of the jurisdiction issue and took this appeal pursuant to 28 U.S.C. § 1292(b) (1976).1

We agree with defendants that there is no federal common law right of action under the circumstances of this litigation. Accordingly, we reverse.

I

The present litigation began in late 1978 and early 1979, when several individual veterans and their families commenced actions in the Northern District of Illinois and the Southern and Eastern Districts of New York, claiming injury from the veterans’ exposure to Agent Orange and purporting to represent several classes of injured persons and persons allegedly “at risk” of injury. The plaintiffs in most of these actions were represented by the same attorney, who filed substantially identical complaints in all actions, naming the same defendant manufacturers. By order of the Judicial Panel on Multidistrict Litigation, thirteen such actions, involving thirty named plaintiffs, were transferred to the Eastern District of New York and assigned to Judge Pratt for coordinated or consolidated pretrial proceedings pursuant to 28 U.S.C. § 1407 (1976). Subsequently, additional actions were filed and were transferred to the Eastern District. It appears that there are presently more than 800 named plaintiffs in these proceedings.

After the transfer plaintiffs filed an amended complaint in the action that the district court had designated as the lead action for purposes of pretrial proceedings. Defendants moved to dismiss on various grounds, and by opinion dated August 14, [989]*9891979, the district court dismissed a number of claims2 and directed that a new complaint be filed. The second amended complaint was filed on August 20, 1979, asserting causes of action under the federal common law3 and premising subject matter jurisdiction on 28 U.S.C. § 1331(a).4 Defendants moved to dismiss for lack of subject matter jurisdiction. The motion was argued on October 3, 1979, and after argument but prior to decision plaintiffs proffered a third amended complaint. Defendants consented to the filing of the new complaint, and the district court, at the urging of the defendants, treated defendants’ motion to dismiss as having been made with respect to that complaint. Accordingly, it is the third amended complaint (hereinafter sometimes referred to as the “Complaint”) that is before us on this appeal.

A. The Third Amended Complaint

The basic thrust of the Complaint is relatively simple: defendants manufactured a “phenoxy herbicide,” Agent Orange, for use by the military in Vietnam. The herbicide was allegedly contaminated with certain toxic organic chemicals, including 2,3,7,8-tetrachlorodibenzo-p-dioxin (“dioxin”), which plaintiffs describe as “one of the most toxic substances ever developed by man.” (Plaintiffs’ Brief on Appeal at 2.) The plaintiff veterans assert that they were exposed to Agent Orange, and thus to the dioxin it contained, while serving in Vietnam. They claim to have sustained various physical injuries, or to be “at risk” of such injuries, by reason of that exposure. Plaintiffs seek relief on a number of theories, including strict product liability, negligence, and breach of warranty.

What marks these proceedings as somewhat extraordinary are the size of the plaintiff class and the scope of the relief that is sought. Plaintiffs purport to represent the 2.4 million veterans who served as combat soldiers in Southeast Asia from 1962 through 1971, as well as most of the families or survivors of those veterans. Fifteen plaintiff subclasses are identified; many of these subclasses consist of persons who are “at risk” of, but have yet to sustain, various physical injuries. Plaintiffs have alleged that “the combined liquid assets of the ‘corporate defendants’ will be insufficient to fully compensate the entire class of plaintiffs.” (Complaint 1 15.) Plaintiffs therefore seek, in addition to unspecified damages,5 a decree requiring defendants, upon a determination of liability, to establish

a trust fund out of the current earnings of the defendants in the nature of a reserve against the claims of all the individual members of the plaintiff class to insure that the compensation of any group of individual plaintiffs will not impair the rights of those not before the Court at that time.

(Complaint H 9.) Plaintiffs also seek a permanent injunction against further manufacture of Agent Orange.

[990]*990Defendants deny that there is any causal connection between exposure to Agent Orange and the injuries that plaintiffs claim to have sustained, and vigorously contest the propriety of the various remedial measures that plaintiffs seek to impose on them. This case, however, is still at the pleading stage, and for purposes of deciding the jurisdictional question before us, plaintiffs’ factual allegations must be accepted as true.

B. The Decision of the District Court

Plaintiffs argue that federal common law should be applied to their claims principally because of the unique federal nature of the relationship between the soldier and his government, relying chiefly on United States v. Standard Oil Co., 332 U.S. 301, 305, 67 S.Ct. 1604, 1606, 91 L.Ed. 2067 (1947) (“Perhaps no relation between the Government and a citizen is more distinctively federal in character than that between it and members of its armed forces.”). They contend that this interest brings the case within the doctrine of Clearfield Trust Co. v. United States, 318 U.S. 363, 366, 63 S.Ct. 573, 574, 87 L.Ed.

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635 F.2d 987, 1980 U.S. App. LEXIS 11998, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-agent-orange-product-liability-litigation-ca2-1980.