Edwards Lifesciences Corporation v. Meril Life Sciences Pvt. Ltd.

District Court, N.D. California·Decided November 18, 2021·No. 4:19-cv-06593·Unknown

Opinion

1 2 3 4 UNITED STATES DISTRICT COURT 5 NORTHERN DISTRICT OF CALIFORNIA 6 7 EDWARDS LIFESCIENCES Case No. 19-cv-06593-HSG CORPORATION, et al., 8 ORDER GRANTING IN PART AND Plaintiffs, DENYING IN PART PLAINTIFFS’ 9 MOTION TO PRECLUDE CERTAIN v. TESTIMONY OF ROBERT VIGIL AND 10 GRANTING AND DENYING MERIL LIFE SCIENCES PVT. LTD., et al., ASSOCIATED ADMINISTRATIVE 11 MOTIONS TO SEAL Defendants. 12 Re: Dkt. Nos. 207, 208, 218, 228, 235

13 Pending before the Court is Plaintiffs Edwards Lifesciences Corporation’s and Edwards 14 Lifesciences LLC’s (collectively “Edwards” or “Plaintiffs”) motion to preclude portions of the 15 testimony of Robert Vigil, the damages expert for Defendants Meril Life Sciences Pvt. Ltd. and 16 Meril, Inc. (collectively “Meril” or “Defendants”). Dkt. No. 208 (“Mot.”). This motion is fully 17 briefed.1 See Dkt. Nos. 236 (“Opp.”), 238 (“Reply”). The parties have also filed associated 18 administrative motions to seal (“Motions to Seal”) portions of their briefs and exhibits. Dkt. Nos. 19 207, 218, 228, 235. For the following reasons, Plaintiffs’ motion to preclude portions of the 20 testimony of Robert Vigil is GRANTED IN PART and DENIED IN PART and their Motions to 21 Seal are DENIED and GRANTED IN PART and DENIED IN PART. 22 I. BACKGROUND 23 Because this case has been actively litigated, the Court limits its review of the factual and 24 procedural background to that relevant to the pending motions. Defendants are an India-based, 25 global medical device company that created a “Myval” branded transcatheter heart valve. Dkt. 26 27 1 No. 98 at 1. Plaintiffs supply medical devices for the treatment of heart disease, including 2 artificial heart valves. Id. at 2. Among their best-known products are their “SAPIEN®” 3 transcatheter prosthetic heart valves. Id. On October 14, 2019, Plaintiffs brought the current 4 lawsuit against Defendants alleging patent infringement, trademark infringement, unfair 5 competition, and false advertising claims relating to the parties’ transcatheter heart valves. Dkt. 6 No. 1 at 25-31. 7 On April 6, 2020, Plaintiffs filed an amended complaint with claims for: (1) Statutory and 8 Common Law Trademark Infringement in violation of 15 U.S.C. § 1114 and the common law; (2) 9 Unfair Competition in violation of 15 U.S.C. § 1125(a); and (3) Unfair Competition and False 10 Advertising in violation of §§ 17200 and 17500 of the California Business and Professions Code. 11 Dkt. No. 51 (or “FAC”) ¶¶ 96-111. For their statutory and common law trademark infringement 12 claim, Plaintiffs allege that Defendants infringed their PARTNER trademark by using the phrase 13 “Partner the Future” at the 2019 TCT Conference in San Francisco; at the 2019 EuroPCR 14 Conference in Paris, France; and in promotional materials related to those two events. Id. ¶¶ 20- 15 22, 49-52. For their Lanham Act and California unfair competition law (UCL) claims, Plaintiffs 16 allege that one of Defendants’ sponsored presentations at the 2018 TCT Conference in San Diego 17 contained incorrect data, and that Defendants made several false or misleading statements at or 18 associated with their presence at the 2019 TCT Conference in San Francisco, the 2019 and 2020 19 EuroPCR Conferences in Paris, France, and the 2019 London Valves Conference in London, 20 England. Id. ¶¶ 41-52. 21 Both parties intend to call expert witnesses to testify about damages. Plaintiffs’ expert 22 witness, Michael Wagner, submitted his report on August 6, 2021, estimating damages for the 23 alleged trademark infringement and alleged false advertising. See Dkt. No. 208-2 (“Wagner 24 Rpt.”). On August 20, 2021, Defendants served Dr. Robert Vigil’s rebuttal damages report, in 25 which he contends that Mr. Wagner’s analysis “suffers from numerous flaws and unsupported 26 assumptions that render his opinion unreliable and vastly overstated.” See Dkt. No. 208-3 (“Vigil 27 Rpt.”) ¶ 40. Dr. Vigil states that he assumes for purposes of his report that Defendants are liable 1 not suffer any economic harm and finds no basis to award them any damages. Id. ¶¶ 2, 40. He 2 further opines that if a trier of fact finds that damages are due, they would be no more than 3 $112,292 for the trademark infringement claim, $93,888 for the false advertising claim, and no 4 more than $152,180 for both claims because the damages overlap. Id. ¶¶ 5, 70. Plaintiffs now 5 move to preclude portions of Dr. Vigil’s testimony under Federal Rule of Evidence 702. 6 II. LEGAL STANDARD 7 Federal Rule of Evidence 702 allows a qualified expert to testify “in the form of an opinion 8 or otherwise” where: 9 (a) the expert’s scientific, technical, or other specialized knowledge 10 will help the trier of fact to understand the evidence or to determine a fact in issue; (b) the testimony is based on sufficient facts or data; 11 (c) the testimony is the product of reliable principles and methods; and (d) the expert has reliably applied the principles and methods to 12 the facts of the case. 13 Fed. R. Evid. 702. Expert testimony is admissible under Rule 702 if the expert is qualified and if 14 the testimony is both relevant and reliable. See Daubert v. Merrell Dow Pharm., Inc., 509 U.S. 15 579, 597 (1993); see also Hangarter v. Provident Life & Acc. Ins. Co., 373 F.3d 998, 1015 (9th 16 Cir. 2004). Rule 702 contemplates a “broad conception of expert qualifications.” Hangarter, 373 17 F.3d at 1018 (emphasis in original). 18 Courts consider a purported expert’s knowledge, skill, experience, training, and education 19 in the subject matter of his asserted expertise. United States v. Hankey, 203 F.3d 1160, 1168 (9th 20 Cir. 2000); see also Fed. R. Evid. 702. Relevance, in turn “means that the evidence will assist the 21 trier of fact to understand or determine a fact in issue.” Cooper v. Brown, 510 F.3d 870, 942 (9th 22 Cir. 2007); see also Primiano v. Cook, 598 F.3d 558, 564 (9th Cir. 2010) (“The requirement that 23 the opinion testimony assist the trier of fact goes primarily to relevance.”) (quotation omitted). 24 Under the reliability requirement, the expert testimony must have a “reliable basis in the 25 knowledge and experience of the relevant discipline.” Primiano, 598 F.3d at 565. To ensure 26 reliability, the Court “assess[es] the [expert’s] reasoning or methodology, using as appropriate 27 such criteria as testability, publication in peer reviewed literature, and general acceptance.” Id. at III. DISCUSSION 1 A. Motion to Preclude Expert Testimony 2 i. References to Underlying Evidence 3 Plaintiffs ask the Court to preclude Dr. Vigil from testifying about certain topics identified 4 in his rebuttal report for four primary reasons. First, Plaintiffs contend that much of Dr. Vigil’s 5 testimony would be unhelpful to the jury because it is not based on specialized expertise and 6 instead regurgitates testimony from other witnesses. See Mot. at 2. 7 “[C]hallenging the assumptions of an expert witness’ report is a permissible topic of 8 rebuttal testimony.” Pinterest, Inc. v.

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Edwards Lifesciences Corporation v. Meril Life Sciences Pvt. Ltd., (N.D. Cal. 2021).

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