Sowers v. Johnson & Johnson Medical, Inc.

867 F. Supp. 306, 1994 U.S. Dist. LEXIS 15830, 1994 WL 631136
CourtDistrict Court, E.D. Pennsylvania
DecidedNovember 1, 1994
Docket2:93-cv-02342
StatusPublished
Cited by19 cases

This text of 867 F. Supp. 306 (Sowers v. Johnson & Johnson Medical, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Sowers v. Johnson & Johnson Medical, Inc., 867 F. Supp. 306, 1994 U.S. Dist. LEXIS 15830, 1994 WL 631136 (E.D. Pa. 1994).

Opinion

OPINION AND ORDER

VAN ANTWERPEN, District Judge.

By motions filed on September 8, 9, and 30, 1994, the defendants in this products liability action filed on May 3,1994 have each moved for summary judgment, asserting that § 136v(b) of the Federal Insecticide, Fungicide, and Rodenticide Act (“FIFRA”), 7 U.S.C. §§ 136-136y, preempts plaintiffs’ claims. This court exercises jurisdiction based on diversity of citizenship under 28 U.S.C. § 1332(a)(1), and venue lies in this district pursuant to 28 U.S.C. § 1391(a)(2). For the reasons stated below, we will grant defendants’ motions.

*308 I. STANDARD OF REVIEW

Rule 56(c) of the Federal Rules of Civil Procedure provides for summary judgment where the

pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any, show that there is no genuine issue of material fact and the moving party is entitled to judgment as a matter of law.

“The party moving for summary judgment must demonstrate that, under the undisputed facts, the non-movant has failed to introduce evidence supporting a necessary element of his ease.” In re Phillips Petroleum Sec. Litig., 881 F.2d 1236, 1243 (3d Cir.1989). To defeat summary judgment, the non-moving party must respond with facts of record that contradict the facts identified by the movant and may not rest on mere denials. See Celotex Corp. v. Catrett, 477 U.S. 317, 321 n. 3, 106 S.Ct. 2548, 2552 n. 3, 91 L.Ed.2d 265 (1986) (quoting Fed.R.Civ.P. 56(e)); see also First Nat’l Bank v. Lincoln Nat’l Life Ins. Co., 824 F.2d 277, 282 (3d Cir.1987). The non-moving party must demonstrate the existence of evidence that would support a jury finding in its favor. See Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248-49, 106 S.Ct. 2505, 2510-11, 91 L.Ed.2d 202 (1986).

II. FACTUAL BACKGROUND

No party disputes the following facts. From 1973 to January .1992 plaintiff Sharon Sowers, a registered nurse, worked at Lancaster General Hospital in Lancaster, Pennsylvania. Her duties there included sterilizing medical equipment using various cold sterilant/disinfectant products containing the chemical glutaraldehyde. These sterilant/ disinfectants were supplied, distributed, manufactured and/or sold by the defendant corporations Johnson & Johnson Medical, Inc. (“Johnson & Johnson”), Metrex Research Corporation (“Metrex”), and Wave Energy Systems (“Wave”). Each product is a “pesticide” within the meaning of FIFRA, and, at all relevant times, was registered with and bore a label approved by the Environmental Protection Agency (“EPA”) as required by FIFRA.

Ms. Sowers now claims that she suffered personal injury as a result of her exposure to the defendants’ products. In the first three counts of her complaint, she advances theories of negligence, strict liability, and breach of express and/or implied warranties. In the fourth count, her husband, plaintiff Harry Sowers, brings a claim for loss of consortium.

III. DISCUSSION

FIFRA requires virtually all pesticides distributed or sold in the United States to be registered with the EPA. See 7 U.S.C. § 136a(a). As part of the registration process, an applicant must submit for EPA approval “a complete copy of the labeling of the pesticide, a statement of all claims to be made for it, and any directions for its use.” Id. at § 136a(c)(l). Before registering a pesticide, the EPA must first determine that its composition is such as to warrant the proposed claims for it, that its labeling complies with the requirements of FIFRA, and that it will perform its intended function “without unreasonable adverse effects on the environment.” See id. at § 136a(c)(5). “The term ‘unreasonable adverse effects on the environment’ means any unreasonable risk to man or the environment, taking into account the economic, social, and environmental costs and benefits of the use of any pesticide.” Id. at § 136(bb). Once the EPA registers a pesticide and approves its label, that label may not be changed without prior EPA approval, except that certain minor changes may be made after merely notifying the EPA. See id. at § 136a(f).

Section 136v of FIFRA, entitled “Authority of States,” provides in relevant part:

(a) In general
A State may regulate the sale or use of any federally registered pesticide or device in the State, but only if and to the extent the regulation does not permit any sale or use prohibited by this subchapter.
(b) Uniformity
Such State shall not impose or continue in effect any requirements for labeling or packaging in addition to or different from those required under this subchapter.

*309 In their motions for summary judgment, defendants contend that part (b) of this section preempts plaintiffs’ claims.

Before addressing the specific question of whether § 136v(b) preempts plaintiffs’ claims, we must first decide the more general question of whether FIFRA’s prohibition against state imposition of “any requirements” for labeling or packaging encompasses the type of “requirements” imposed by state common law causes of action. Defendants contend that it does. Plaintiffs, on the other hand, advance a much narrower reading of the section. They urge the Court to adopt the reasoning of Ferebee v. Chevron Chem. Co., 736 F.2d 1529 (D.C.Cir.), cert. denied, 469 U.S. 1062, 105 S.Ct. 545, 83 L.Ed.2d 432 (1984), in which the D.C. Circuit held that § 136v(b) does not preempt common law actions, but instead merely prohibits states from directly ordering changes in EPA-approved labels, as for example, through injunctions or statutory regulation of pesticide labeling. The Court finds that the applicable law supports defendants’ reading.

The Supreme Court has not yet defined the preemptive scope of § 136v(b), and neither has the Third Circuit. In 1989, a judge of our Court ruled that FIFRA

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Bluebook (online)
867 F. Supp. 306, 1994 U.S. Dist. LEXIS 15830, 1994 WL 631136, Counsel Stack Legal Research, https://law.counselstack.com/opinion/sowers-v-johnson-johnson-medical-inc-paed-1994.