Giordano v. MARKET AMERICA, INC.

599 F.3d 87, 2010 U.S. App. LEXIS 5672, 2010 WL 944177
CourtCourt of Appeals for the Second Circuit
DecidedMarch 17, 2010
DocketDocket 06-2071-cv
StatusPublished
Cited by120 cases

This text of 599 F.3d 87 (Giordano v. MARKET AMERICA, INC.) 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
Giordano v. MARKET AMERICA, INC., 599 F.3d 87, 2010 U.S. App. LEXIS 5672, 2010 WL 944177 (2d Cir. 2010).

Opinion

SACK, Circuit Judge:

Plaintiff John Giordano appeals from a judgment of the United States District Court for the Southern District of New York (Jed S. Rakoff, Judge) in a personal injury action filed by Giordano against defendants Market America, Inc., and The Chemins Company, Inc. Giordano alleges that dietary supplements containing the substance ephedra that the defendants supplied caused his March 1999 cerebral aneurism and subsequent medical events. On April 10, 2006, the district court granted summary judgment for the defendants on the grounds that Giordano’s lawsuit, filed on July 28, 2003, was barred by the three-year statute of limitations set forth in N.Y. C.P.L.R. § 214. See In re Ephedra Prods. Liab. Litig., Nos. 04 M.D. 1598, 05 Civ. 1018, 2006 WL 944705, at *1, 2006 U.S. Dist. LEXIS 18691, at *1-2 (S.D.N.Y. Apr.10, 2006) (“Ephedra II”). The court concluded that the one-year extension of the statute of limitations provided for in N.Y. C.P.L.R. § 214-c(4) for situations in which the cause of the injury was not discovered during the original three-year period to file suit was inapplicable because section 214-c(4) is limited to latent injuries and that injuries caused by ephedra were not latent. Id.

The plaintiff appealed from the district court’s judgment and we heard oral argument on November 8, 2007. On August 18, 2008, we remanded for the limited purpose of asking the district comb to determine whether a genuine issue of material fact existed as to whether an additional requirement of N.Y. C.P.L.R. § 214-c(4) had been met, namely that Giordano “allege and prove that technical, scientific or medical knowledge and information sufficient to ascertain the cause of his injury had not been discovered, identified or determined” prior to the expiration of the otherwise applicable three-year statute of limitations. See Giordano v. Mkt. Am., Inc., 289 Fed.Appx. 467, 469 (2d Cir.2008) (summary order). On February 24, 2009, in response to our question and with expressed doubt as to the standard to be applied under New York law, the district court concluded that under any possible standard there was a genuine issue of material fact as to whether sufficient information had been “discovered, identified or determined” at the relevant time. See In re Ephedra Prods. Liab. Litig., 598 *90 F.Supp.2d 535, 537 (S.D.N.Y.2009) (“Ephedra III”).

The applicability of N.Y. C.P.L.R. § 214 — c(4) to Giordano’s claims is now before this Court again. The resolution of this issue requires us to answer three separate questions of New York law: (1) Are the provisions of N.Y. C.P.L.R. § 214-c(4) providing for an extension of the statute of limitations in certain circumstances limited to actions for injuries caused by the latent effects of exposure to a substance?; (2) Can an injury that occurs within 24 to 48 hours of exposure to a substance be considered “latent” for these purposes?; (3) What standards should be applied to determine whether a genuine issue of material fact exists for resolution by a trier of fact as to whether “technical, scientific or medical knowledge and information sufficient to ascertain the cause of [the plaintiffs] injury” was “discovered, identified or determined” for N.Y. C.P.L.R. § 214-e(4) purposes? Resolving the third question requires us to decide both the level of certainty required for knowledge to be deemed “sufficient to ascertain” the cause of an injury, and the community that must possess this knowledge — that is, whether the knowledge must be reasonably available to a plaintiff and his or her lawyers, or whether it must be reasonably available to the scientific, technical, or medical community.

In this instance, the district court found that “some studies suggesting a possible connection between ephedra and injuries similar to Giordano’s were published in reputable scientific journals that were publicly available” during the three-year period after discovery of Giordano’s injury, but that there was “a lack of awareness of the risks by even the most interested members of the public” during that time. Ephedra III, 598 F.Supp.2d at 537 n. 1.

The three questions of statutory interpretation raised by this appeal have not been answered conclusively by New York courts. They, in turn, implicate questions of public policy pertaining to how the New York Legislature intended to balance the rights of those suffering personal injuries with the rights of defendants and with the need for judicial economy. New York courts are better situated to answer these questions than are we. We therefore certify them to the New York Court of Appeals.

BACKGROUND

Pursuant to an order of the Judicial Panel on Multidistriet Litigation, see 28 U.S.C. § 1407, the district court that decided this case is charged with managing some 500 civil actions, including this one, involving claims of “personal injury or wrongful death caused by dietary supplements containing ephedra.” In re Ephedra Prods. Liab. Litig., 393 F.Supp.2d 181, 184 (S.D.N.Y.2005) (“Ephedra /”). Ephedra is a plant containing “ephedrine alkaloids.” Id. at 185. Until relatively recently, products containing ephedra were widely used by consumers seeking “weight loss, increased energy and improved athletic performance.” Id.; see also id. at 189 n. 4.

The Food, Drug, and Cosmetic Act (“FDCA”) prohibits “[t]he introduction or delivery for introduction into interstate commerce of any food ... that is adulterated. ...” 21 U.S.C. § 331(a). Section 402 of the FDCA provides that a “food shall be deemed to be adulterated ... [i]f it is a dietary supplement or contains a dietary ingredient that ... presents a significant or unreasonable risk of illness or inju ry____” Id. § 342(f)(1)(A). On February 11, 2004, the United States Food and Drug Administration (“FDA”) effectively banned ephedra by declaring dietary supplements *91 containing ephedrine alkaloids “adulterated” under the FDCA. See 21 C.F.R. § 119.1; Final Rule Declaring Dietary Supplements Containing Ephedrine Alkaloids Adulterated Because They Present an Unreasonable Risk (“FDA Final Rule”), 69 Fed.Reg. 6788 (Feb. 11, 2004). This rule became effective on April 12, 2004. Id.

The district court’s opinion in Ephedra I

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Bluebook (online)
599 F.3d 87, 2010 U.S. App. LEXIS 5672, 2010 WL 944177, Counsel Stack Legal Research, https://law.counselstack.com/opinion/giordano-v-market-america-inc-ca2-2010.