Ruhe v. Masimo Corp.

14 F. Supp. 3d 1342, 2014 WL 1599466, 2014 U.S. Dist. LEXIS 57445
CourtDistrict Court, C.D. California
DecidedApril 3, 2014
DocketCase No. SACV 11-00734-CJC(JCGx)
StatusPublished

This text of 14 F. Supp. 3d 1342 (Ruhe v. Masimo Corp.) is published on Counsel Stack Legal Research, covering District Court, C.D. California primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ruhe v. Masimo Corp., 14 F. Supp. 3d 1342, 2014 WL 1599466, 2014 U.S. Dist. LEXIS 57445 (C.D. Cal. 2014).

Opinion

ORDER GRANTING DEFENDANT’S MOTION TO VACATE FINAL ARBITRATION AWARD

CORMAC J. CARNEY, District Judge.

I. INTRODUCTION

In September 2011, the Court ordered the parties to arbitrate Plaintiffs Michael Ruhe and Vicente Catala’s claims that they were constructively discharged from Defendant Masimo Corporation because of undue pressure Masimo placed on them to sell its medical devices despite allegedly knowing that the devices were inaccurate and defective. Thirty-six hours before the final hearing in the arbitration, Masimo’s counsel made a for-cause challenge to the continued service of the arbitrator, Retired Justice Richard C. Neal (the “Arbitrator”) of Judicial Arbitration and Mediation Services (“JAMS”). The challenge was based on Masimo’s recent discovery that the Arbitrator’s brother had represented its chief competitor in two highly contentious litigation losses to Masimo with liability verdicts totaling over half a billion dollars. Instead of having the challenge heard by JAMS as required by JAMS’s rules, the Arbitrator himself determined that he was not subject to disqualification and issued his final award, imposing $5 million in punitive damages against Masimo. This large punitive damage award, more than 16 times the compensatory damage award, was based in part on what the Arbitrator characterized as “abusive litigation tactics” by Masimo’s counsel in the arbitration, including the fact that Masimo’s counsel sought his disqualification. Masimo now moves to vacate the arbitration award. (Dkt. No. 49.) After considering the evidence presented by the parties and carefully reviewing the Arbitrator’s written decision, the Court concludes that the arbitration award must be vacated. The Arbitrator demonstrated evident partiality by awarding excessive and improper punitive damages in retaliation for Masimo’s counsel challenging his impartiality and taking other reasonable measures to zealously represent their client.1

[1344]*1344II. BACKGROUND

Masimo develops, manufactures, and sells non-invasive patient-monitoring medical devices. (Dkt. No. 51 [“Everton Decl.”] Exh. 2 [“Final Award”] at 4-5.) Its first and leading category of products are devices known as pulse oximeters. Pulse oximeters, first introduced in the 1980s, measure oxygen saturation in the blood (“Sp02”) by analyzing wavelengths of light through a sensor clipped to the patient’s finger. Previously, measuring blood oxygen required drawing a blood sample from the patient and sending it away to be analyzed in a laboratory. Early pulse oximeters were susceptible to inaccurate readings when the patient moved or had low blood flow. Masimo’s founders invented advanced sensor technology that provided reliable readings under these conditions, and this technology became the basis for its pulse oximetry devices. Masi-mo’s latest line of devices measure an additional blood constituent known as total hemoglobin (“SpHb”). The first of these devices, the Radical-7, was cleared by the Food and Drug Administration (“FDA”) in May 2008. (Final Award at 8.) The devices primarily at issue in this action are the Pronto and Pronto-7 (together, the “Pronto Devices”), and were cleared by the FDA in October 2008 and June 2010, respectively. (Id.)

Plaintiffs were hired as sales representatives at Masimo in December 2008 and March 2009. (Id.) They were two of the sales representatives assigned to sell the new line of Pronto Devices. Plaintiffs experienced difficulty getting physicians and clinics to buy the new devices, which Plaintiffs attributed to problems with device accuracy. For instance, Mr. Ruhe did a product demonstration of the Pronto during a sales call with two doctors in January 2009, and the device displayed “significant variations in back to back readings among several doctors.” (Id.) The doctors did not purchase the device. According to Plaintiffs, they reported to Masimo their difficulty selling the devices because of physicians’ concerns about accuracy, but their complaints were met with “pressure and insistence that the [sales representatives] continue their efforts to sell the devices.” (Id. at 13.) Plaintiffs’ sales of the devices “had fallen off drastically” by mid-2010, and they were put on remedial performance plans. (Id. at 14.) In August 2010, Plaintiffs consulted an attorney, Mr. Bona-gofsky, who would subsequently represent them in this action. (Id. at 19.) In October 2010, Plaintiffs downloaded thousands of Masimo documents and then resigned from the company. (Id. at 16-17.) Plaintiffs submitted their resignation letters on October 22, 2010. One week later, Plaintiffs filed their complaint against Masimo in the related action, United States ex rel. Michael Ruhe, et al. v. Masimo Corporation, Case No. SACV 10-08169-CJC(VBKx) (the “Qui Tam Action”).

In the Qui Tam Action, Plaintiffs sought damages from Masimo under the Federal False Claims Act, 31 U.S.C. § 3729 et seq., asserting that Masimo made misrepresentations to the FDA and medical providers in connection with the Pronto Devices. Plaintiffs alleged, inter alia, that Masimo made misrepresentations regarding the devices’ FDA-cleared indications for use, misrepresentations regarding validation studies, and misrepresentations regarding the devices’ ability to perform to their FDA-cleared accuracy specification.2 (See Qui Tam Action, Dkt. No. 52 at 14-15.)

[1345]*1345Seven months after filing the Qui Tam Action, Plaintiffs filed their complaint in this employment case.3 Plaintiffs asserted claims for constructive discharge in violation of the whistleblower protections of the Dodd-Frank Wall Street Reform and Consumer Protection Act of 2010, 15 U.S.C. § 78u-6(h); retaliation in violation of California Labor Code section 1102(c); “wrongful constructive termination” in violation of public policy; and unfair competition in violation of California Business and Professions Code section 17200 et seq.4 (Final Award at 25-29; Dkt. No. 1 [“Compl.”].) The Court compelled the employment action to arbitration on September 16, 2011, 2011 WL 4442790. At some point in the proceeding, the arbitration apparently evolved into a plenary review of Masimo’s medical devices and the minutiae of the company’s compliance with FDA regulations. The parties were allowed to present evidence over ten days of hearings before the Arbitrator in early February 2013. Closing arguments were held in July 2013.

Meanwhile, the Qui Tam Action was proceeding in parallel. Pursuant to the scheduling order, trial was set for October 29, 2013, and all motions had to be heard by September 20, 2013. (See Qui Tam Action, Dkt. No. 52.) In light of the motion deadline, Masimo filed its motion for summary judgment on August 19, 2013, set for hearing on September 16, 2013. (Qui Tam Action, Dkt. No. 117.) The Court issued its order granting Masimo’s motion for summary judgment on October 2. 2013. (See Qui Tam Action, Dkt. No. 255.) The Court found that Plaintiffs failed to demonstrate any knowingly misleading statements or conduct by Masimo in connection with the Pronto Devices. (Id.

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14 F. Supp. 3d 1342, 2014 WL 1599466, 2014 U.S. Dist. LEXIS 57445, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ruhe-v-masimo-corp-cacd-2014.