Jasper v. Abbott Laboratories, Inc.

834 F. Supp. 2d 766, 2011 WL 2672519, 2011 U.S. Dist. LEXIS 73806
CourtDistrict Court, N.D. Illinois
DecidedJuly 8, 2011
DocketCase No. 11 C 229
StatusPublished
Cited by6 cases

This text of 834 F. Supp. 2d 766 (Jasper v. Abbott Laboratories, Inc.) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Jasper v. Abbott Laboratories, Inc., 834 F. Supp. 2d 766, 2011 WL 2672519, 2011 U.S. Dist. LEXIS 73806 (N.D. Ill. 2011).

Opinion

MEMORANDUM OPINION AND ORDER

VIRGINIA M. KENDALL, District Judge.

Plaintiff Chalonda L. Jasper (“Jasper”) brought a class action suit on behalf of herself and others similarly situated against Abbott Laboratories, Inc. (“Abbott”). Jasper alleges six counts relating to the contamination of Abbott’s Similac infant formula, including intentional and [769]*769negligent misrepresentation; a violation of the Indiana Deceptive Consumer Sales Act, Ind.Code §§ 24-5-0.5 (“DCSA”); breaches of express and implied warranties; and unjust enrichment. Abbott moves to dismiss Jasper’s Complaint. For the following reasons, the Court grants Abbott’s motion and dismisses Jasper’s Complaint without prejudice.

STATEMENT OF FACTS

The following facts are taken from Jasper’s Complaint and are assumed to be true for purposes of this Motion to Dismiss. See Murphy v. Walker, 51 F.3d 714, 717 (7th Cir.1995).

Jasper, an Indiana resident, purchased a container of Abbott’s Similac Advance Early Shield Powder infant formula on Sept. 18, 2010 and began feeding the formula to her son. (Compl. ¶¶ 8, 10.) Roughly four days later, around Sept. 22, 2010, Abbott announced that it was recalling more than five million containers of formula because the product may have been contaminated with beetles or beetle larvae. (Compl. ¶¶ 20, 22.) The container Jasper purchased was one of the 2,000-plus lot numbers recalled. (Compl. ¶ 22.) The Food and Drug Administration found that infants who ingested the formula contaminated with beetles or beetle larvae experienced gastrointestinal discomfort and temporary refusal to eat. (Compl. ¶ 2.) At the time of the recall, Jasper’s son had eaten about half of the container of formula. (Compl. ¶ 10.) As a result of the contamination, Jasper and class members suffered “extreme mental anguish and pain and suffering.” (Compl. ¶¶ 38, 46.) Jasper does not allege that her son suffered any physical injury.

Abbott’s Sturgis, Michigan manufacturing facility has a history of beetle infestation. (Compl. ¶ 26.) In a Department of Health and Human Services (“DHHS”) Inspection Report, DHHS found approximately 30 instances of beetles in the facility between 2007 and 2010. (Compl. ¶ 27.) In July 2010, Abbott received a complaint from a consumer who found insects in her Similac formula. (Compl. ¶ 29.) One month later, in August 2010, Abbott received another consumer complaint regarding a weevil found in the formula. (Compl. ¶ 30.)

Abbott marketed the Similac formula as one that “Moms can count on for trusted nutrition and formula that’s right for their babies.” (Compl. ¶ 17.) Abbott also advertised the formula with statements including:

• “When it comes to the science of nutrition, Similac stands apart.”
• “More moms choose Similac. Why? Similac Advance has EarlyShield, and is designed to be more like breast milk and help support your baby’s developing immune system. Only EarlyShield has our patented blend of immune-supporting nucleotides — plus prebiotics and carotenoids, nutrients naturally found in breast milk.”
• “Nearly 100 years and 280 clinical studies have nourished our most advanced formulas. No wonder it’s the # 1 brand fed in hospitals-and the choice of more moms.”
• “You can trust Similac Sensitive to provide a strong start for your baby’s developing digestive system.”
• “It’s no wonder that a company with such a heritage of innovation was the company to bring moms Similac Advance. Whether they’re formula feeding or supplementing their breast milk, they can be confident knowing that Similac Advance is designed to be more like breast milk and to help build a strong immune system.”

[770]*770(Compl. ¶ 19.) Jasper alleges that, based on these statements, she bought Similac Advance Early Shield Powder infant formula and fed it to her son. (Compl. ¶ 25.)

STANDARD OF REVIEW

When considering a motion to dismiss under Rule 12(b)(6), the Court accepts as true all facts alleged in the complaint and construes all reasonable inferences in favor of the plaintiff. See Murphy, 51 F.3d at 717. To state a claim upon which relief can be granted, a complaint must contain a “short and plain statement of the claim showing that the pleader is entitled to relief.” Fed.R.Civ.P. 8(a)(2). “Detailed factual allegations” are not required, but the plaintiff must allege facts that, when “accepted as true ... ‘state a claim to relief that is plausible on its face.’ ” Ashcroft v. Iqbal, 556 U.S. 662, 129 S.Ct. 1937, 1949, 173 L.Ed.2d 868 (2009) (quoting Bell Atlantic Corp. v. Twombly, 550 U.S. 544, 555, 127 S.Ct. 1955, 167 L.Ed.2d 929 (2007)). In analyzing whether a complaint has met this standard, the “reviewing court [must] draw on its judicial experience and common sense.” Id. at 1950. When there are well-pleaded factual allegations, the Court assumes their veracity and then determines if they plausibly give rise to an entitlement to relief. Id. A claim has facial plausibility when the pleaded factual content allows the Court to draw a reasonable inference that the defendant is liable for the misconduct alleged. See id. at 1949.

Claims alleging fraud must also satisfy Rule 9(b), which requires that “[i]n all averments of fraud or mistake, the circumstances constituting fraud or mistake shall be stated with particularity.” Fed. R.Civ.P. 9(b). “While [Rule 9(b) ] does not require a plaintiff to plead facts that if true would show that the defendant’s alleged misrepresentations were indeed false, it does require the plaintiff to state ‘the identity of the person making the misrepresentation, the time, place, and content of the misrepresentation, and the method by which the misrepresentation was communicated to the plaintiff.’ ” Uni*Quality, Inc. v. Infotronx, Inc., 974 F.2d 918, 923 (7th Cir.1992). The heightened pleading therefore requires a complaint alleging fraud to contain more substance to survive a motion to dismiss as compared to a Rule 12(b)(6) motion based on another cause of action. See Ackerman v. Nw. Mut. Life Ins. Co., 172 F.3d 467, 469 (7th Cir.1999) (stating that Rule 9(b) forces “the plaintiff to do more than the usual investigation before filing his complaint”); Vicom, Inc. v. Harbridge Merch. Servs., Inc., 20 F.3d 771, 777 (7th Cir.1994) (explaining that “[t]he rule is said to serve three main purposes: (1) protecting a defendant’s reputation from harm; (2) minimizing ‘strike suits’ and ‘fishing expeditions’; and (3) providing notice of the claim to the adverse party”).

DISCUSSION

I. Misrepresentation

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834 F. Supp. 2d 766, 2011 WL 2672519, 2011 U.S. Dist. LEXIS 73806, Counsel Stack Legal Research, https://law.counselstack.com/opinion/jasper-v-abbott-laboratories-inc-ilnd-2011.