Medical Wind Down Holdings III, Inc. v. InnerDyne, Inc. (In Re Medical Wind Down Holdings III, Inc.)

332 B.R. 98, 2005 Bankr. LEXIS 1896, 45 Bankr. Ct. Dec. (CRR) 128, 2005 WL 2456261
CourtUnited States Bankruptcy Court, D. Delaware
DecidedOctober 5, 2005
Docket17-12826
StatusPublished
Cited by4 cases

This text of 332 B.R. 98 (Medical Wind Down Holdings III, Inc. v. InnerDyne, Inc. (In Re Medical Wind Down Holdings III, Inc.)) is published on Counsel Stack Legal Research, covering United States Bankruptcy Court, D. Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Medical Wind Down Holdings III, Inc. v. InnerDyne, Inc. (In Re Medical Wind Down Holdings III, Inc.), 332 B.R. 98, 2005 Bankr. LEXIS 1896, 45 Bankr. Ct. Dec. (CRR) 128, 2005 WL 2456261 (Del. 2005).

Opinion

MEMORANDUM OPINION

PETER J. WALSH, Bankruptcy Judge.

In this adversary proceeding defendant InnerDyne, Inc.’s (“InnerDyne”) motion (Doc. # 6) seeks to dismiss the three counts of plaintiff Medical Wind Down Holdings III, Inc.’s (Pk/a Maxxim Medical, Inc.) (“Maxxim”) complaint. For the reasons set forth below, InnerDyne’s motion will be denied.

BACKGROUND

On February 11, 2003, Maxxim and its related entities filed voluntary petitions for relief under chapter 11 of title 11 of the United States Code, 11 U.S.C. §§ 101 et seq. (the “Bankruptcy Code”). On October 28, 2003, this Court approved the sale of substantially all of Maxxim’s assets. On November 10, 2003, the sale closed and Maxxim ceased all ongoing business operations. On May 17, 2004, the Court confirmed Maxxim’s plan of liquidation.

The instant matter arises out of a dispute between Maxxim and InnerDyne over certain actions taken by the parties during Maxxim’s prepetition business operations. On February 2, 2000, InnerDyne sent Maxxim a letter (the “February Letter”) describing a novel proprietary vascular access method (the “Device”). When Maxx-im received the February Letter, it was in the business of developing, manufacturing, and marketing specialty medical products. The letter indicated that due to Inner-Dyne’s limited synergies with its distribution channel, InnerDyne was interested in pursuing a strategic marketing and distribution alliance with Maxxim. This alliance would allow both parties to take full advantage of InnerDyne’s innovation.

*101 The February Letter advised that this innovation promised to shorten a patient’s stay in the hospital after a vascular access procedure. To do this, the Device used radial dilation to prevent blunt trauma to the vein. This method would minimize the puncture wound associated with the insertion of a vascular access device; the smaller the puncture wound, the shorter the patient’s hospital stay. (Doc. # 1, Exh. A).

The February Letter represented that the Device achieved such results without any vascular access complications. Further, the February Letter stated that In-nerDyne had conducted over 400 test cases in the United States and Europe and had completed a pilot study at the William Beaumont Hospital. According to Inner-Dyne, the results of these clinical tests had shown that the Device could achieve at least a 50% reduction in time to ambulation without any increase in vascular access complications. (Doc. # 1, Exh. A).

Less than two months after receiving the February Letter, Maxxim agreed to the proposed strategic alliance with Inner-Dyne by entering into the Supply, License and Distribution Agreement (“the Agreement”). Maxxim’s complaint alleges that the Device did not work as promised because it failed to decrease patient recovery time. Further, Maxxim alleges that the Device provided no benefits to either patient or doctor. As a result, Maxxim states it was unable to successfully market the Device.

The complaint asserts that InnerDyne led Maxxim to believe that substantial testing, clinical evaluations, and reliable data supported InnerDyne’s representations of the Device’s benefits. Maxxim alleges that such representations were false and that InnerDyne knew that such representations were false when made or, alternatively, that InnerDyne made such representations with reckless disregard for their veracity.

These representations, which Maxxim allegedly relied on, are said to have materially impacted the sale of the Device and resulted in harm to Maxxim. Accordingly, Maxxim claims that but for such misrepresentations, it would not have entered the Agreement with InnerDyne. In addition, Maxxim asserts that InnerDyne failed to supply it with a Device that was “free from defects in all respects” under the terms of the Agreement. Thus, the complaint contains claims for fraud in the inducement, negligent misrepresentation, and breach of contract.

By its motion, InnerDyne argues that the complaint should be dismissed pursuant to Federal Rules of Civil Procedure 12(b)6 and 9(b). 1 InnerDyne asserts that the complaint fails to state a claim for fraud or negligent misrepresentation because Maxxim has not alleged a false representation of material fact and Maxxim cannot establish justifiable reliance as a matter of law. Also, InnerDyne asserts that the complaint fails to state a claim for breach of contract because Maxxim has not alleged a defect that is covered by the Agreement and Maxxim has faded to satisfy all conditions precedent. Maxxim contests all of these assertions.

Section 11(a) of the Agreement provides that the governing law is the State of Delaware.

DISCUSSION

A motion to dismiss for failure to state a claim upon which relief can be granted under Federal Rule 12(b)(6) serves to test the sufficiency of the complaint. Kost v. Kozakiewicz, 1 F.3d 176, 183 (3d Cir.1993). *102 When deciding such a motion, a court accepts as true all allegations in the complaint and draws all reasonable inferences from it which the court considers in a light most favorable to the plaintiff. Morse v. Lower Merion Sch. Dist., 132 F.3d 902, 906 (3d Cir.1997); Rocks v. City of Phila., 868 F.2d 644, 645 (3d Cir.1989). A court should not grant a Rule 12(b)(6) motion “unless it appears beyond doubt that the plaintiff can prove no set of facts in support of his claim which would entitle him to relief.” Conley v. Gibson, 355 U.S. 41, 45-46, 78 S.Ct. 99, 102, 2 L.Ed.2d 80 (1957).

Federal Rule of Civil Procedure 9(b) requires that in “all averments of fraud or mistake, the circumstances constituting fraud or mistake shall be stated with particularity.” FED. R. CIV. P. 9(b). The purpose of this rule is to “place the defendants on notice of the precise misconduct with which they are charged ....” Seville Indus. Mach. Corp. v. Southmost Mach. Corp., 742 F.2d 786, 791 (3d Cir.1984).

The allegations, as discussed below, are sufficiently stated as to put InnerDyne on notice to the specific misconduct alleged.

A successful claim of fraud must establish: “1) a false representation, usually one of fact, made by the defendant; 2) the defendant’s knowledge or belief that the representation was false, or was made with reckless indifference to the truth; 3) an intent to induce the plaintiff to act or to refrain from acting; 4) the plaintiffs action or inaction taken in justifiable reliance upon the representation; and 5) damage to the plaintiff as a result of such reliance.” Stephenson v. Capano Dev., Inc., 462 A.2d 1069, 1074 (Del.1983).

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332 B.R. 98, 2005 Bankr. LEXIS 1896, 45 Bankr. Ct. Dec. (CRR) 128, 2005 WL 2456261, Counsel Stack Legal Research, https://law.counselstack.com/opinion/medical-wind-down-holdings-iii-inc-v-innerdyne-inc-in-re-medical-wind-deb-2005.