prod.liab.rep. (Cch) P 15,173 Martha Haddix v. Playtex Family Products Corporation

138 F.3d 681, 1998 U.S. App. LEXIS 4033, 1998 WL 97245
CourtCourt of Appeals for the Seventh Circuit
DecidedMarch 6, 1998
Docket97-2074
StatusPublished
Cited by15 cases

This text of 138 F.3d 681 (prod.liab.rep. (Cch) P 15,173 Martha Haddix v. Playtex Family Products Corporation) is published on Counsel Stack Legal Research, covering Court of Appeals for the Seventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
prod.liab.rep. (Cch) P 15,173 Martha Haddix v. Playtex Family Products Corporation, 138 F.3d 681, 1998 U.S. App. LEXIS 4033, 1998 WL 97245 (7th Cir. 1998).

Opinion

BAUER, Circuit Judge.

In this products liability case, removed to federal court on the basis of diversity of citizenship, plaintiff Martha Haddix (“Had-dix”) appeals from the district court’s grant of summary judgment to defendant Playtex Family Products Corporation (“Playtex”). She presently argues that the district court’s decision was erroneous arid should be reversed. As discussed below, we find that the district court properly determined that summary judgment for the defendant was appropriate, and we affirm.

BACKGROUND

On December 3, 1990, Haddix was hospitalized for several days after experiencing a high fever, chills, coughing, vomiting, diarrhea, and aches all over her body. Haddix was informed that she had contracted Toxic Shock Syndrome (“TSS”), and that she should never use tampons again. TSS is a disease caused by a toxin produced by the Staphylococcus aureus bacteria, the growth of which can occur in tampons. In the week prior to her hospitalization, Haddix had used Playtex Portable super absorbency tampons for spotted menstrual bleeding. On Friday, November 30, Haddix felt ill, prompting her to leave work early and go to the hospital. After undergoing some tests, she was released and diagnosed with the flu. Over the next few days, her symptoms persisted and worsened, leading to Haddix’s hospitalization and the eventual diagnosis that she suffered from TSS.

In response to her illness, Haddix filed suit against Playtex on December 3, 1992, in the Circuit Court of Edgar County, Illinois. Playtex (and then-defendant K-Mart, who was later dismissed from the suit) removed the case to the United States District Court for the Central District of Illinois on January 5,1993. After a rather confusing procedural history and the filing of several motions for summary judgment by Playtex, Chief Judge Michael M. Mihm granted summary judgment to Playtex on all remaining issues on March 26, 1997. Final judgment was entered the same day, and Haddix filed a timely notice of appeal on April 24,1997. In this appeal, Haddix argues that Judge Mihm erroneously granted summary judgment to Playtex on those parts of her complaint which alleged that the Playtex tampons used by Haddix were unreasonably dangerous and caused her to suffer from TSS and asserted that Playtex was strictly liable for her injuries. Haddix alleged that the super-absorbent tampons made by Playtex contained synthetic fiber as well as natural fiber, rendering them more likely to promote the growth of TSS-causing bacteria. With this brief history in mind, we turn to Haddix’s contentions.

DISCUSSION

We review the district court’s grant of summary judgment de novo. McGinn v. Burlington Northern Ry. Co., 102 F.3d 295, 298 (7th Cir.1996) (citation omitted). Summary judgment is appropriate where “the pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any, show that there is no *683 genuine issue as to any material fact and that the moving party is entitled to judgment as a matter of law.” Fed.R.Civ.P. 56(c); see Celotex Corp. v. Catrett, 477 U.S. 317, 322-23, 106 S.Ct. 2548, 2552-53, 91 L.Ed.2d 265 (1986). We view the record and extract all reasonable inferences from it in the light most favorable to the nonmoving party. McGinn, 102 F.3d at 298 (citation omitted). Only disputes that could affect the outcome of the suit under governing law will preclude an entry of judgment for the moving party. Id.

The parties seem to agree that this products liability ease is governed by Illinois law. Illinois has adopted the strict liability formula set forth in Restatement (Second) of Torts § 402A (1965) (hereinafter “Restatement”). Lamkin v. Towner, 138 Ill.2d 510, 150 Ill.Dec. 562, 569-70, 563 N.E.2d 449, 457 (1990). Accordingly, strict liability is imposed on anyone who sells any product in a defective condition unreasonably dangerous to consumers, users, or their property. Martin v. Harrington and Richardson, Inc., 743 F.2d 1200, 1202 (7th Cir.1984); Restatement § 402A. A product may be considered unreasonably dangerous for two reasons: 1) because of a design or manufacturing defect, or 2) because of a failure to warn consumers of a danger posed by the product of which the average consumer would not already be aware. Martin, 743 F.2d at 1202; Lamkin, 150 Ill.Dec. at 569-70, 563 N.E.2d at 457. In her brief, Haddix concedes that the failure to warn prong is inapplicable here, i since all failure to warn arguments are preempted in the context of tampon products liability cases by 21 U.S.C. § SdOlsfa), 1 part of the Medical Device Amendments of 1976 to the Federal Food, Drug, and Cosmetic Act (21 U.S.C. §§ 301 et seq.), and also by corresponding sections of the Code of Federal Regulations (e.g., 21 C.F.R. § 808.1(b)). Seé Appellant’s Brief at 9. Accordingly, we examine Haddix’s arguments regarding the design or manufacture of the Playtex tampons.

In order tó state a cause of action for strict products liability in Illinois, the plaintiff must show that: 1) an injury resulted from the condition of the product; 2) the condition of the product was unreasonably dangerous; and 3) the condition existed at the time that the product left the manufacturer’s control. Hunt v. Blasius, 74 Ill.2d 203, 23 Ill.Dec. 574, 578, 384 N.E.2d 368, 372 (1979) (citing Suvada v. White Motor Co., 32 Ill.2d 612, 210 N.E.2d 182 (1965)). Under the Restatement approach to strict liability, a product is considered unreasonably dangerous when it is “dangerous to an extent beyond that which would be contemplated by the- ordinary consumer who purchases it, with the ordinary knowledge common to the community as to its characteristics.” Id. (quoting Restatement § 402A, cmt. i (other citations omitted)). This test has come to be known as the “consumer contemplation” test. Todd v. Societe Bic, S.A., 21 F.3d 1402, 1406 (7th Cir.) (en banc), cert. denied, 513 U.S. 947, 115 S.Ct. 359, 130 L.Ed.2d 312 (1994).

' [5] Under the Restatement, the consumer contemplation test was the only standard authorized for determining whether a product was unreasonably dangerous.

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