Bryceland v. Minogue

557 F. App'x 1
CourtCourt of Appeals for the First Circuit
DecidedJune 10, 2014
Docket13-1914
StatusUnpublished
Cited by1 cases

This text of 557 F. App'x 1 (Bryceland v. Minogue) is published on Counsel Stack Legal Research, covering Court of Appeals for the First Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Bryceland v. Minogue, 557 F. App'x 1 (1st Cir. 2014).

Opinion

SOUTER, Associate Justice.

Marta Bryceland appeals the dismissal of her shareholder derivative action brought on behalf of Abiomed, Inc. Because Bryceland’s complaint fails to plead with the required particularity that a demand to the directors for remedial action would have been futile, we affirm.

On defendants’ motion to dismiss under Fed.R.Civ.P. 12(b)(6), the following facts are taken as stated in the complaint. Abiomed is a Delaware corporation with its principal place of business in Massachusetts. It develops products to assist or replace the pumping of the human heart, and the company’s promotion of one such device, the Impelía 2.5, led to this lawsuit.

In June 2011, a letter to Abiomed from the Food and Drug Administration (FDA) alleged that some advertising materials appeared to market the Impelía 2.5 for uses that the FDA had not approved. Abiomed publicly disclosed its receipt in the company’s later mandatory quarterly filing with the Securities and Exchange Commission (SEC):

[W]e received a warning letter from the FDA stating that some of our promotional materials marketed the Impelía 2.5 for uses that had not been approved by the FDA. We have cooperated with the FDA in addressing its concerns and believe that we have resolved the matter without any penalties. Although we believe that this issue has been resolved, if similar matters come up in the future, we may not be able to resolve them without facing significant consequences. Such matters could result in reduced demand for our products and would have a material adverse effect on our operations and prospects.

In April 2012, the FDA wrote to Abiomed again alleging that some Impelía 2.5 promotional materials continued to violate FDA regulations. Abiomed’s next SEC filing disclosed this letter as well:

*2 In June 2011 we received a warning letter from the FDA stating that some of our promotional materials marketed the Impelía 2.5 for uses that had not been approved by the FDA. We cooperated with the FDA and made changes to our promotional materials in response to the warning letter. However, in April 2012, we received a follow up letter from the FDA stating that some of our promotional materials continued to market the Impelía 2.5 in ways that are not compliant with FDA regulations. We are cooperating with the FDA in addressing its concerns. While we hope to be able to resolve this matter without incurring penalties, we may not be able to resolve it, or any similar matters that may come up in the future without facing significant consequences. Such matters could result in reduced demand for our products and would have a material adverse effect on our operations and prospects.

In October 2012, Abiomed received a subpoena from the U.S. Attorney’s Office for the District of Columbia, which was investigating Abiomed’s marketing materials. Abiomed made the subpoena known in a special press release:

On October 26, 2012, Abiomed was informed that the United States Attorney’s Office for the District of Columbia is conducting an investigation that is focused on the Company’s marketing and labeling of the Impelía 2.5. On October, 31, 2012, Abiomed accepted service of a Health Insurance Portability and Accountability Act administrative subpoena related to this investigation. The subpoena seeks documents related to the Impelía 2.5 and we understand the investigation focuses primarily on marketing and labeling issues. Abiomed is in the process of responding to the subpoena and intends to cooperate fully.

A sharp drop in Abiomed’s stock price followed. Some four months later, and after this lawsuit had been brought, the FDA wrote Abiomed that the agency had completed its evaluation and that the company had addressed the problems to the agency’s satisfaction. The current status of the U.S. Attorney’s investigation is unknown. At oral argument, defendants’ counsel represented that Abiomed has heard nothing from the U.S. Attorney’s Office since responding to the subpoena.

Bryceland, an Abiomed shareholder, brought this derivative action in federal court on behalf of the corporation against its seven directors, one of whom is also the President and CEO. Bryceland’s overarching theory, running through the multiple counts of the complaint, is that the defendants breached their fiduciary duties to Abiomed because, with them at the helm, the company both unlawfully marketed the Impelía 2.5 and issued public statements that were overly sunny in the face of the corporation’s potential liability. Bryceland takes particular exception to the fact that, in the intervals between the unfavorable disclosures, the directors approved the issuance of press releases of positive financials without reiterating cautions about the potential liability associated with the FDA inquiry.

Defendants moved to dismiss the complaint on the grounds that it failed both to plead with particularity that a demand for corrective action would have been futile, and to state a claim of substantive liability. The district court dismissed for want of a particularized futility allegation. 1

*3 Among other things, Bryceland says that the district court failed to accept her allegations as true, to treat them collectively, and to draw inferences in her favor. But because our review of the dismissal of a derivative suit for failure to plead with particularity is de novo, see Union de Empleados de Muelles de P.R. PRSSA Welfare Plan v. UBS Fin. Servs. Inc. of P.R., 704 F.3d 155, 162-63 (1st Cir.), cert. granted, — U.S. -, 133 S.Ct. 2857, 186 L.Ed.2d 908, and cert. dismissed, — U.S. -, 134 S.Ct. 40, 186 L.Ed.2d 954 (2013), rather than answer each of Bryceland’s assignments of error, it will suffice to highlight the deficiencies in her complaint. We accept as true all well-pleaded facts and draw all reasonable inferences in her favor. Mass. Ret. Sys. v. CVS Caremark Corp., 716 F.3d 229, 237 (1st Cir.2013).

A derivative action permits a shareholder to enforce corporate rights that the corporation itself is unable or unwilling to enforce on its own. See Union de Empleados, 704 F.3d at 159. Before invoking this procedural device a shareholder must demand that the corporation take action, unless such a demand would be futile, and the shareholder’s complaint must accordingly either state that her demand was rebuffed (or inadequately honored) or explain why a demand would have proven pointless. See id. In such a case, despite the relative laxity of pleading requirements generally, see Fed.R.Civ.P. 8(a)(2), a special rule governing derivative actions requires the complaint to “state with particularity” the shareholder’s efforts to make a demand or her reasons for failing to do so, id. 23.1(b)(3).

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Bluebook (online)
557 F. App'x 1, Counsel Stack Legal Research, https://law.counselstack.com/opinion/bryceland-v-minogue-ca1-2014.