Merisant Co. v. McNeil Nutritionals, LLC

242 F.R.D. 303, 2007 U.S. Dist. LEXIS 27676, 2007 WL 1118387
District Court, E.D. Pennsylvania·Decided April 9, 2007·No. Civil Action No. 04-5504·Published·Cited by 6 cases

Opinion

Memorandum and Order

PRATTER, District Judge.

Merisant Company, Inc. (“Merisant”) alleges that McNeil Nutritionals, LLC and McNeil-PPC, Inc. (collectively, “McNeil”) engaged in false and misleading advertising with respect to its Splenda No Calorie Sweetener product in violation of Section 43(a) of the Lanham Act, 15 U.S.C. § 1125, and the Pennsylvania common law of unfair competition. A jury trial is scheduled to begin on April 9, 2007. The parties have engaged in extensive discovery activities and recently exchanged pretrial memoranda, leading to their submission of numerous motions in limine, in which they argue, among other things, that certain evidence should be excluded under Rules 402 and 403 of the Federal Rules of Evidence.

Factual and Procedural Background

The factual and procedural background of this action was recited in detail in the Court’s March 2, 2007 Memorandum and Opinion [306]*306(Docket No. 152), and will not be repeated here. Any factual and procedural history that is relevant to the pending motions will be discussed below.

Standard

“Under the Federal Rules of Evidence, subject to certain limitations, all evidence is admissible if it is relevant, i.e., if it tends to make the existence or nonexistence of a disputed material fact more probable than it would be without that evidence.” Forrest v. Beloit Corp., 424 F.3d 344, 355 (3d Cir.2005); see Fed.R.Evid. 401, 402. Pursuant to Rule 403, a court may nonetheless exclude relevant evidence if the probative value of the evidence is “substantially outweighed by the danger of unfair prejudice, confusion of the issues, or misleading the jury, or by considerations of undue delay, waste of time, or needless presentation of cumulative evidence.” Forrest, 424 F.3d at 355 (quoting Fed.R.Evid. 403). The Court of Appeals for the Third Circuit has described Rule 403 as an “ ‘umbrella rule’ spanning the whole of the Federal Rules of Evidence,” and as such district courts must apply Rule 403 “in tandem with other Federal Rules under which evidence would be admissible.” Id. (quoting Coleman v. Home Depot, Inc., 306 F.3d 1333, 1343 (3d Cir.2002)). A district court must articulate the Rule 403 balancing — the probative value of potentially relevant evidence must be “carefully balanced, pursuant to Rule 403, against its possible prejudicial effect.” Id. at 356. “ ‘Rule 403 recognizes that a cost/benefit analysis must be employed to determine whether or not to admit evidence; relevance alone does not ensure its admissibility.’ ” Id. (quoting Coleman, 306 F.3d at 1343). In the Third Circuit there is a “strong presumption” that relevant evidence should be admitted. Id. A party arguing that evidence should be excluded under Rule 403 must show that “the probative value of evidence must be ‘substantially outweighed’ by the problems in admitting it.” Id. (quoting Coleman, 306 F.3d at 1343-44). However, “ ‘prejudice does not simply mean damage to the opponent’s cause.’ ” Goodman v. Pa. Turnpike Comm’n, 293 F.3d 655, 670 (3d Cir.2002) (quoting 1 McCormick on Evidence § 185 at 645 (John W. Strong, et al. eds., 5th ed.1999)). Only “unfair prejudice” can tip the scales in favor of inadmissibility:

The ... prejudice against which the law guards [is] ... unfair prejudice — ... prejudice of the sort which cloud[s] impartial scrutiny and reasoned evaluation of the facts, which inhibit[s] neutral application of principles of law to the facts as found____ Prejudice does not simply mean damage to the opponent’s cause. If it did, most relevant evidence would be deemed prejudicial.

Ansell v. Green Acres Contr. Co., 347 F.3d 515, 525 (3d Cir.2003) (quoting Wagenmann v. Adams, 829 F.2d 196, 217 (1st Cir.1987)).

Discussion

A. McNeil’s Motion to Exclude Inflammatory and Irrelevant Evidence Concerning the Sucralose Manufacturing Process (Docket No. 164)

McNeil seeks to exclude inflammatory and irrelevant statements regarding the manufacturing process for Sucralose and Splenda. McNeil argues that Merisant intends to improperly refer to certain “toxic” or “hazardous” chemicals that may be used in the manufacturing process for Splenda. In addition, McNeil fears that Merisant intends to overdramatize McNeil’s chemical process for manufacturing Splenda in explaining such process to the jury.

It is beyond question that the details of McNeil’s manufacturing process for Splenda is relevant in this case inasmuch as Meri-sant’s literal falsity claim rests substantially on its argument that Splenda’s “sugar-like” taste results from Splenda’s manufacturing process and not from its sugar origins. A detailed, yet fair, reasonable and accurate description of the manufacturing process for Splenda is therefore appropriate. The Court finds that McNeil will not suffer any unfair prejudice as a result of this evidence being introduced.

However, the Court acknowledges what seems to be one of McNeil’s main concerns here, namely, that any reference to “toxic” chemicals would improperly impugn Splen-da’s safety for human consumption. Meri-sant does not argue that Splenda is unsafe, and any attempt to imply as much through [307]*307the use of gratuitous, cumulative and inflammatory language, such as applying the labels “toxic” or “hazardous” (or synonyms therefor), is impermissible. Therefore, McNeil’s motion will be granted in part and denied in part.

B. Merisant’s Motion in limine No. 6 to Exclude any Evidence or Argument Regarding Government “Approval” of Sucrose or Splenda’s Advertising or Marketing (Docket No. 180)

Merisant seeks to exclude evidence that any government agency, specifically the U.S. Food & Drug Administration (“FDA”), has “approved” McNeil’s marketing or advertising for Splenda. Specifically, Merisant argues that McNeil’s intends to introduce evidence that the FDA “approved” certain labeling, use of words or concepts, or packaging for Splenda.

McNeil argues that such information is relevant to rebut Merisant’s argument that McNeil engaged in an “evolutionary” marketing campaign. In this regard, McNeil intends to argue that in 1990, when it initially approached the FDA about approving Splen-da for certain consumer uses, McNeil portrayed Splenda as capitalizing on its sugar “origins,” and that McNeil has consistently focused on such origins ever since.

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Merisant Co. v. McNeil Nutritionals, LLC, 242 F.R.D. 303, 2007 U.S. Dist. LEXIS 27676, 2007 WL 1118387 (E.D. Pa. 2007).

242 F.R.D. 303 (Merisant Co. v. McNeil Nutritionals, LLC) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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