Wilco AG v. Packaging Technologies & Inspection LLC

615 F. Supp. 2d 320, 2009 U.S. Dist. LEXIS 42923, 2009 WL 1391025
CourtDistrict Court, D. Delaware
DecidedMay 19, 2009
DocketCiv. 08-635-SLR
StatusPublished
Cited by1 cases

This text of 615 F. Supp. 2d 320 (Wilco AG v. Packaging Technologies & Inspection LLC) is published on Counsel Stack Legal Research, covering District Court, D. Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wilco AG v. Packaging Technologies & Inspection LLC, 615 F. Supp. 2d 320, 2009 U.S. Dist. LEXIS 42923, 2009 WL 1391025 (D. Del. 2009).

Opinion

MEMORANDUM OPINION

SUE L. ROBINSON, District Judge.

I. INTRODUCTION

Plaintiff Wilco AG (“plaintiff’) brought this patent infringement action against defendant Packaging Technologies & Inspection LLC (“PTI” or “defendant”) on September 30, 2008. (D.I. 1) Plaintiff and defendant are competitors in the market for package leak testing products. Plaintiff asserts that defendant infringes U.S. Patent Nos. 5,907,093 (“the '093 patent”) and 6,305,215 (“the '215 patent”), both relating generally to products and methods for testing closed and filled containers for leaks. Defendant asserts the affirmative defenses of laches, “waiver and estoppel,” and unclean hands. Defendant also asserts counterclaims for a declaratory judgment of invalidity (based generally upon a failure to comply with “35 U.S.C. §§ 102, 103, and/or 112”), unenforceability due to inequitable conduct, noninfringement, and tortious interference with prospective business relations. (D.I. 8) Presently before the court is plaintiffs motion to dismiss defendant’s counterclaims of inequitable conduct and tortious interference with business relations. (D.I. 9) The court has jurisdiction pursuant to 28 U.S.C. §§ 1338(a) and 1367. For the reasons that follow, the court grants in part and denies in part plaintiffs motion.

II. BACKGROUND

Plaintiff, a Swedish company, is the owner by assignment of the '093 and '295 patents. (D.I. 1 at ¶¶ 1, 9) Defendant is a Delaware corporation with its principal place of business in Tuckahoe, New York. (D.I. 8 at ¶ 28) Defendant is a former United States distributor for plaintiffs products. The parties had a working relationship until “early 2008.” (D.I. 10 at 2; D.I. 13 at 3)

In March 2008, defendant introduced its own leak tester for empty and pre-filled medical syringes and vials called the “Veri-Pac 325/LV.” In its press release, defendant stated that the VeriPac 325/LV detects as little as 0.1 microliters of vapor or gas release. Additionally, defendant stated that “[t]he VeriPac 325/LV core technology is based on the ASTM vacuum decay leak test method (F2338) recognized by the FDA as a consensus standard for package integrity testing.” (D.I. 10, ex. A) Plaintiff filed this infringement suit on September 30, 2008.

Plaintiff and defendant are active members in the Parenteral Drug Association (“PDA”). The PDA hosted a conference in San Diego, California on October 6 and 7, 2008, entitled “The Universe of Pre-filled Syringes and Injection Devices.” (D.I. 13, ex. C) At the conference, Dr. Dana Guazzo (“Guazzo”), an expert in the field of leak testing, gave a presentation entitled “Nondestructive Container Closure Integrity Test for Pre-filled Syringes.” (Id. at 4) As part of her lecture, Guazzo presented the results of ASTM round-robin tests for the PTI 325/LV vacuum decay method (F2338) *323 for detecting leaks in pre-filled syringes. (Id., ex. D) Guazzo endorsed defendant’s method as “more sensitive” and “more reliable” than older (dye ingress) test methods. (Id., ex. D at 15)

Prior to Guazzo’s presentation, on October 2, 2008, Gerhard Schramm (“Schramm”), plaintiffs director of sales, sent an email to Linda McCoy (“McCoy”) and Shawn Kinney of the PDA. Schramm’s email stated in relevant part:

It has come to our attention that at the upcoming PDA conference ... a presentation will be provided by Dr. Dana Guazzo concerning leak testing devices and methods [ ]. Based on Dr. Guazzo’s previous presentations, we believe that Dr. Guazzo intends to attribute ownership of certain leak testing technology to [PTI] and to make reference to PTI’s VeriPac 325 product.
I wish to advise that Wilco has recently instituted a suit for infringement by PTI of Wilco’s ['093 and '215 patents] in the District of Delaware, which addresses PTI’s unauthorized appropriation of Wilco’s patented leak testing technology. In keeping with this organization’s laudable efforts to promote global sharing of knowledge and innovation through an unbiased forum for the exchange of industry perspectives and concerns, we respectfully request that any reference to PTI and its products in Dr. Guazzo’s presentation be promptly removed.

(Id, ex. G)

McCoy emailed Guazzo the following day, October 3, 2008, noting that eight of Guazzo’s presentation slides appeared to contain information referenced by Schramm’s email, and stating that “[u]n-less you can present a strong argument that suggests] that you are legally privileged to present this information, on behalf of PDA and the Universe of Prefilled Syringes [and] Injection Devices Program Planning Committee, I am asking you to remove those slides.” (Id, ex. H) Guazzo thereafter engaged in discussions with Jennifer Ikeda (“Ikeda”) of PDA. In the afternoon of October 3, 2008, Ikeda informed McCoy that Guazzo “respectfully can stand behind her presentation because it is a scientific paper of test results on the PTI test equipment and model, as defined by ASTM.” (Id, ex. I) Guazzo, therefore, gave her unabridged presentation at the conference as planned on October 6, 2008.

Prior to the October 2008 presentation, Guazzo gave a presentation (in January 2008) at the “Pre-filled Syringes Forum 2008” in Philadelphia, Pennsylvania. (Id, ex. E) Guazzo’s January presentation was entitled “Novel Nondestructive Approach for Integrity Testing Empty and Pre-filled Syringes.” (Id) Guazzo discussed several advantages to PTI’s “new” VeriPac technology, including the 0.1 microliter detection limit. (D.I. 10, ex. D) The technology was described as “unique to PTI.” (Id, ex. D at 24) Plaintiff states that Guazzo’s January 2008 presentation prompted Schramm’s October 2, 2008 email to the PDA in advance of the October 2008 conference. (Id at 4)

III. STANDARD OF REVIEW

In reviewing a motion filed under Federal Rule of Civil Procedure 12(b)(6), the court must accept all factual allegations in a complaint as true and take them in the light most favorable to plaintiff. See Erickson v. Pardus, 551 U.S. 89, 127 S.Ct. 2197, 2200, 167 L.Ed.2d 1081 (2007); Christopher v. Harbury, 536 U.S. 403, 406, 122 S.Ct. 2179, 153 L.Ed.2d 413 (2002). A complaint must contain “a short and plain statement of the claim showing that the pleader is entitled to relief, in order to give the defendant fair notice of what the ... claim is and the grounds upon which it rests.” Bell Atl. Corp. v. Twombly, 550 U.S. 544, 554-55, 127 S.Ct. 1955, 167 *324

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615 F. Supp. 2d 320, 2009 U.S. Dist. LEXIS 42923, 2009 WL 1391025, Counsel Stack Legal Research, https://law.counselstack.com/opinion/wilco-ag-v-packaging-technologies-inspection-llc-ded-2009.