United States of America v. Medtronic Inc

CourtDistrict Court, D. Minnesota
DecidedJanuary 16, 2018
Docket0:17-cv-03770
StatusUnknown

This text of United States of America v. Medtronic Inc (United States of America v. Medtronic Inc) is published on Counsel Stack Legal Research, covering District Court, D. Minnesota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States of America v. Medtronic Inc, (mnd 2018).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MINNESOTA Civil No.: 17-3770(DSD/TNL) United States of America, ex rel., and Cavallino Consulting LLC, Relator, Plaintiffs, v. ORDER Medtronic, Inc., Defendant. Adam M. Shapiro, Esq. and Cotchett, Pitre & McCarthy, 840 Malcolm Road, Burlingame, CA 94010, counsel for plaintiff. Dulce J. Foster, Esq. and Fredrikson & Byron, PA 200 South 6th Street, Suite 4000, Minneapolis, MN 55402, counsel for defendant.

This matter is before the court upon the motion to dismiss by defendant Medtronic, Inc. Based on a review of the file, record, and proceedings herein, and for the following reasons, the motion is granted. BACKGROUND This qui tam action arises from relator Cavallino Consulting, LLC’s claim that since 2012 Medtronic has fraudulently charged hospitals owned and operated by the federal government for expedited shipping costs it did not actually incur. Relator is a consulting firm based in California that conducts audits, known as Transportation Overcharge Recovery Audits, of health care systems to “uncover transportation overcharging.” Compl. ¶ 8. Medtronic is a medical device manufacturer that sells products to hospitals throughout the country.1 Id. ¶ 11. Relator alleges that, through ten years of audits, it discovered that Medtronic has engaged in a widespread scheme to “overcharge for expedited shipping across various health care systems.” Id. ¶ 10. Relator does not allege that it audited a government hospital or entity or that it otherwise investigated Medtronic’s sales to the government in reaching that conclusion. Nor does relator identify representative examples of sales in which Medtronic overcharged the government for expedited shipping. See Compl. Ex. 1. Relator nevertheless alleges that Medtronic receives substantial discounts on expedited shipping from various carriers that it failed to pass on to the government despite its contractual obligation to do so. Compl. ¶ 21. Relator broadly estimates that the discounts ranged from 35% to 65%, which resulted in millions of

dollars in overpayment by the government. Id. ¶¶ 2, 21. The contract attached to the complaint is an “f.o.b. destination” contract which, the parties agree, means that the listed prices include the cost of delivery. Compl. Ex. 1 ¶ 15. The contract also provides, however, that for expedited, overnight,

1 The complaint mistakenly asserts that Medtronic’s headquarters are in Illinois rather than Minnesota. Compl. ¶ 11. This error is apparently a stray allegation from a nearly identical complaint filed by relator against a medical device manufacturer based in Illinois. The complaint also erroneously refers to Medtronic as “defendants,” which is also presumably due to relator’s other similar lawsuits. 2 and two-day delivery, the government is “responsible for the additional shipping charge[s] between the normal surface (ground) rate and expedited rate.” Id. ¶¶ 11b, 11c. The parties disagree as to the meaning of this provision. According to relator, it requires the government to pay the actual expedited shipping costs paid by Medtronic, whereas Medtronic interprets it to mean that the government is required to pay the expedited shipping “rate” notwithstanding any carrier discounts. According to relator, the contract language is sufficiently clear to establish that Medtronic knowingly presented false claims for payment to the government by submitting invoices that included expedited shipping costs it did not actually incur due to carrier discounts. Compl. ¶¶ 23-24. On September 10, 2015, relator commenced this suit against Medtronic in the Central District of California alleging violations of the False Claims Act (FCA), 31 U.S.C. § 3729(a)(1)(A), (B), and

(G). The government declined to intervene. ECF No. 19. Medtronic moved to transfer the case to Minnesota and to dismiss. ECF Nos. 34, 35. The California court granted the transfer motion finding that convenience and fairness were best served by transferring the case to Minnesota. ECF No. 41, at 2-4. The court declined to entertain the motion to dismiss given the pending transfer.2 Id. at 4. Medtronic now moves to dismiss all claims against it under

2 The motion to dismiss was fully briefed and substantively identical to the instant motion. See ECF Nos. 35, 36, 39. 3 Federal Rules of Civil Procedure 9(b) and 12(b)(6). Relator requests the opportunity to file an amended complaint should the court find that its pleading is insufficient.

DISCUSSION I. Standard To survive a motion to dismiss for failure to state a claim, “‘a complaint must contain sufficient factual matter, accepted as true, to state a claim to relief that is plausible on its face.’” Braden v. Wal-Mart Stores, Inc., 588 F.3d 585, 594 (8th Cir. 2009) (quoting Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009)). “A claim

has facial plausibility when the plaintiff [has pleaded] factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Iqbal, 556 U.S. at 678 (citing Bell Atl. Corp. v. Twombly, 550 U.S. 544, 556 (2007)). Although a complaint need not contain detailed factual allegations, it must raise a right to relief above the speculative level. Twombly, 550 U.S. at 555. “[L]abels and conclusions or a formulaic recitation of the elements of a cause of action” are not sufficient to state a claim. Iqbal, 556 U.S. at 678 (citation and internal quotation marks omitted). Here, because all of relator’s claims are based in fraud, each must also meet the heightened pleaded requirements of Rule 9(b). See U.S. ex rel. Joshi v. St. Luke’s Hosp., Inc., 441 F.3d 552, 556

4 (8th Cir. 2006) (“Because the FCA is an anti-fraud statute, complaints alleging violations of the FCA must comply with Rule 9(b).”). The requirements of Rule 9(b) are read “in harmony with the principles of notice pleading,” and the level of particularity required depends upon the nature of a case. Schaller Tel. Co. v. Golden Sky Sys., Inc., 298 F.3d 736, 746 (8th Cir. 2002) (citation and internal quotation marks omitted). However, “[c]onclusory allegations that a defendant’s conduct was fraudulent and deceptive are not sufficient to satisfy the rule.” Id. (citation and internal quotation marks omitted). To satisfy the heightened pleading requirement, a plaintiff must set forth the “who, what, where, when, and how” of an alleged fraud. Joshi, 441 F.3d at 556 (citation and internal quotation marks omitted). In other words, a plaintiff must plead “the time, place and contents of false representations, as well as the identity of the person making the

misrepresentation and what was obtained or given up thereby.” BJC Health Sys. v. Columbia Cas. Co., 478 F.3d 908, 917 (8th Cir. 2007) (citation and internal quotation marks omitted). II. Adequacy of Complaint The FCA imposes liability against any person who knowingly presents a false or fraudulent claim for payment to the federal government.3 31 U.S.C. § 3729(a)(1). The FCA allows private

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United States of America v. Medtronic Inc, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-of-america-v-medtronic-inc-mnd-2018.