Walsingham v. Biocontrol Technology, Inc.

66 F. Supp. 2d 669, 1998 U.S. Dist. LEXIS 20897, 1998 WL 1114054
CourtDistrict Court, W.D. Pennsylvania
DecidedDecember 1, 1998
DocketCivil Action 96-809
StatusPublished
Cited by2 cases

This text of 66 F. Supp. 2d 669 (Walsingham v. Biocontrol Technology, Inc.) is published on Counsel Stack Legal Research, covering District Court, W.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Walsingham v. Biocontrol Technology, Inc., 66 F. Supp. 2d 669, 1998 U.S. Dist. LEXIS 20897, 1998 WL 1114054 (W.D. Pa. 1998).

Opinion

*673 MEMORANDUM OPINION

CINDRICH, District Judge.

This class action lawsuit arises from alleged violations of federal securities laws. The plaintiff filed a two count complaint asserting the following claims: Count One, violation of Section 10(b) of the Securities Exchange Act (the “Exchange Act”), 15 U.S.C. Section 78j(b), and Rule 10b-5 promulgated thereunder, 17 C.F.R. Section 240.10b-5, against all defendants; and Count Two, violation of Section 20(a) of the Exchange Act, 15 U.S.C. Section 78t(a), against defendants Biocontrol Technology, Inc., David. L. Purdy, and Fred E. Cooper. Pending before the court is the defendants’ Motion To Dismiss Pursuant To Fed. R.Civ.P. 9(b) and 12(b)(6). 1

I. Backgrmmd 2

The plaintiff brought this action as a class action pursuant to Fed.R.Civ.P. 23, on behalf of a class of purchasers of the common stock of defendant Biocontrol Technology, Inc. (“BICO”), to recover damages arising from the defendants’ alleged violations of Sections 10(b) and 20(a) of the Exchange Act. The court entered an order on March 14, 1997, certifying the action as a class action on behalf of all persons who purchased the common stock of BICO during the period between April 25,1995 and February 26,1996. 3

BICO is a Pennsylvania corporation engaged in the development and manufacture of biomedical devices and environmental products. BICO has approximately 37 million shares of issued and outstanding stock which trades on the NASDAQ Exchange. BICO, together with defendant Diasense, Inc. (“Dia-sense”), a Pennsylvania corporation and 52% owned subsidiary of BICO, is one of a group of companies engaged in the development of a biomedical testing device for the non-invasive monitoring of glucose levels in the blood of people with diabetes. Defendant David L. Purdy (“Pur-dy”) is the President, Chairman of the Board, and Treasurer of BICO and an officer and director of Diasense. Defendant Fred E. Cooper (“Cooper”) is the Chief Executive Officer, Executive Vice President, and a director of BICO and a director of Diasense. Defendant Glenn Keeling (“Keeling”) is the Vice President of Marketing and a director of BICO.

BICO claims that its device, the Diasen-sor 1000 Noninvasive Glucose Sensor (the “Diasensor 1000”), eliminates the pain and inconvenience associated with traditional testing methods. The Diasensor 1000 allegedly allows diabetics to test themselves by passing infrared light beams through the forearm which detects the level of glucose and passes that information to a computer for comparison with a patient profile. Diasense is the owner and marketer of the Diasensor 1000, while BICO *674 has the exclusive manufacturing rights to the product.

BICO began developing the Diasensor 1000 about a decade ago and on January 6, 1994 the company filed a 510(k) Notification with the FDA. A 501(k) Notification is an application for FDA approval which seeks to obtain approval by establishing that the device to be marketed is substantially equivalent to a legally marketed device that was, or is, currently on the U.S. market (a “predicate”). The FDA’s Division of Clinical Laboratory Devices accepted BICO’s 510(k) application for review by its Clinical Chemistry/Toxicology branch. BICO has not, however, received FDA clearance for the Diasensor 1000.

The Diasensor 1000 is essentially BICO’s only product. Accordingly, BICO has suffered substantial losses and is unable to generate revenue to finance its operations, including development and testing costs for the Diasensor 1000. Thus, BICO sells stock to finance its existence, including the payment of executive salaries which rank among the highest in their class.

The plaintiff alleges that the defendants knowingly created a false impression that BICO was ready to begin the marketing phase of the Diasensor 1000 and was poised to capture the market for non-invasive glucose testing. Citing to numerous examples, the plaintiff contends that throughout the class period the defendants issued misleading press releases and made misleading public statements touting the Diasensor 1000’s effectiveness and reliability and projecting its imminent approval by the FDA. The defendants allegedly made such representations even though BICO had not conducted the necessary testing to obtain FDA approval.

The plaintiff contends that the defendants’ alleged misrepresentations had the effect of inflating BICO’s stock until the lack of testing and poor test results of the Diasensor 1000 were revealed in a public hearing before an FDA panel on February 26, 1996. As a result, BICO shares fell 41%.

II. Analysis

A. Motion to Dismiss Pursuant To Fed.R.Civ.P. 9(b)

The defendants argue that the complaint should be dismissed for failing to meet the pleading requirements of Fed.R.Civ.P. 9(b) and Section 21D(b) of the Exchange Act, 15 U.S.C. Section 78u-4(b)(l) and (2).

Section 10(b) claims sound in fraud, thus, the allegations of fraud must be stated with particularity pursuant to Fed.R.Civ.P. 9(b). In re Westinghouse Securities Litigation, 90 F.3d 696, 710 (3d Cir.1996) (citation omitted). “Rule 9(b) requires a plaintiff to plead (1) a specific false representation of material fact; (2) knowledge by the person who made it of its falsity; (3) ignorance of its falsity by the person to whom it was made; (4) the intention that it should be acted upon; and (5) that the plaintiff acted upon it to his damage.” Id. (citation and quotation omitted).

A plaintiff must also satisfy the heightened pleading requirements of Section 21D(b) of the Exchange Act, which provides at 15 U.S.C. Section 78u-4(b)(l) that:

In any private action arising under this chapter in which the plaintiff alleges that the defendant -
(A) made an untrue statement of a material fact; or
(B) omitted to state a material fact necessary in order to make the statements made, in the light of the circumstances in which they were made, not misleading;

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Cite This Page — Counsel Stack

Bluebook (online)
66 F. Supp. 2d 669, 1998 U.S. Dist. LEXIS 20897, 1998 WL 1114054, Counsel Stack Legal Research, https://law.counselstack.com/opinion/walsingham-v-biocontrol-technology-inc-pawd-1998.