In Re Subpoenas

692 F. Supp. 2d 602, 2010 U.S. Dist. LEXIS 21947, 2010 WL 841258
CourtDistrict Court, W.D. Virginia
DecidedMarch 10, 2010
DocketMisc. Action 1:10mc00001
StatusPublished
Cited by1 cases

This text of 692 F. Supp. 2d 602 (In Re Subpoenas) is published on Counsel Stack Legal Research, covering District Court, W.D. Virginia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Subpoenas, 692 F. Supp. 2d 602, 2010 U.S. Dist. LEXIS 21947, 2010 WL 841258 (W.D. Va. 2010).

Opinion

MEMORANDUM OPINION

SAMUEL G. WILSON, District Judge.

This is a motion by the United States to compel compliance with two subpoenas issued to Abbott Laboratories (“Abbott”) pursuant to 18 U.S.C. § 3486, which authorizes the Attorney General or his designee to issue subpoenas “in any investigation relating to any act or activity involving a federal health care offense.” Abbott refused to comply on the ground that the subpoenas are unreasonable and unduly burdensome. The United States has agreed to limit the scope of the subpoenas. The court has concluded that, as limited, the subpoenas are sufficiently limited in scope, relevant in purpose, and specific in directive so that compliance will not be unreasonably burdensome. Accordingly, the court enforces them as limited.

I.

Abbott is a publicly traded manufacturer of pharmaceuticals, medical devices, and nutritional products. It operates in over 100 countries, has nearly 72,000 employees, and annual sales of nearly $30 billion. In 1982, the Food and Drug Administration (“FDA”) approved Abbott’s new drug Depakote for the treatment of bipolar disorder, epileptic seizures, and migraines. The United States is investigating Abbott for a number of potential federal violations arising out of Abbott’s impermissible off-label marketing of Depakote as a treatment for agitation and aggression in the elderly, and health care fraud arising out of that allegedly improper use. Earlier, the government issued a number of subpoenas, and the parties were able to resolve their differences without the court’s intervention. Abbott has since refused to comply with two subpoenas it claims are unduly burdensome. Those subpoenas seek all e-mails sent or received by thirteen individuals from 1996 through 2008. The government has offered to limit those subpoenas to the e-mails of only three people (William Dempsey, Miles White, and Jeffrey Leiden) relating to Depakote and off-label marketing of other FDA approved drugs. Abbot can satisfy the subpoena by producing (1) the “live e-mails” sent or received by each of the three individuals relating to Depakote and off-label marketing of other FDA approved drugs and, (2) the e-mails of each of those individuals relating to Depakote and off-label marketing of other FDA approved drugs retrieved from a single snapshot from “backup tapes” for each of the years 2002 through 2008. According to Abbott, this will require Abbott to restore 53 (out of 32,300) backup tapes 1 that were preserved for other litigation. Abbott estimates that it will cost “roughly $750” for each backup tape, “approximately $10,000 to establish the back-up environment, ... any engineering required to access the data or troubleshoot” at the rate of $240 per hour, and “anywhere from $350-$650” for each gigabyte of restored data to place it in reviewable format (with each tape containing “5-10 gigabytes of data potentially responsive to the subpoenas for e-mails”).

II.

Abbott maintains that it is prohibitively expensive to restore the yearly, snapshot e-mails of the three individuals, despite the fact that the requested records were necessarily retained for other litigation. This requires the court to determine whether *604 the subpoenas are “sufficiently limited in scope, relevant in purpose, and specific in directive so that compliance will not be unreasonably burdensome.” See v. City of Seattle, 387 U.S. 541, 544, 87 S.Ct. 1737, 18 L.Ed.2d 943 (1967). The court concludes that the subpoenas, as limited by the government, are not unreasonably burdensome, and the court will enforce them.

The Fourth Amendment imposes a reasonableness standard on subpoenas. See In Re Subpoena Duces Tecum, 228 F.3d 341 (4th Cir.2000). To satisfy the reasonableness standard, a subpoena must be issued for a legitimate and authorized governmental purpose, and it must be relevant to the inquiry. Id. at 349. The “legitimate and authorized governmental purpose prohibits the government from ‘engaging in arbitrary fishing expeditions’ and from ‘selecting targets of investigation out of malice or an intent to harass.’ ” Id. (citing United States v. R. Enters., Inc., 498 U.S. 292, 299, 111 S.Ct. 722, 112 L.Ed.2d 795 (1991)). The court will not enforce a subpoena that is “far too sweeping” or not “suitably specific and properly limited in scope,” if the person served has sought but has not received a reasonable accommodation from the government narrowing the scope of that subpoena. Id. (internal citations omitted). In summary, to be reasonable under the Fourth Amendment, an investigative subpoena must be:

(1) authorized for a legitimate governmental purpose; (2) limited in scope to reasonably relate to and further its purpose; (3) sufficiently specific so that a lack of specificity does not render compliance unreasonably burdensome; and (4) not overly broad for the purpose of the inquiry as to be oppressive....

Id. at 349. However, the recipient of an investigative subpoena has the burden of proving that the subpoena, as limited, is unreasonable. See Oklahoma Press Publ’g Co. v. Walling, 327 U.S. 186, 218, 66 S.Ct. 494, 90 L.Ed. 614 (1946). Abbott has failed to meet that burden.

Here, Abbott does not contest that the subpoenas were authorized for a legitimate governmental purpose, but it does contest the relevance of e-mails relating to off-label marketing of all FDA approved drugs (other than Depakote), and it contends that it would be unreasonably burdensome for it to comply. The court rejects those challenges.

First, as to relevance, Abbott itself recognizes that the off-label marketing of Depakote is highly relevant to the government’s investigation. The same also appears to be true as to the off-label marketing of other drugs. The government has indicated that it has evidence that the off-label marketing of other FDA approved drugs may have followed a similar pattern to the off-label marketing of Depakote. 2 If this is' so, the off-label marketing of these other drugs may raise the same related health care fraud issues that the marketing of Depakote raises. 3

*605 Second, the court does not credit Abbott’s argument that the two subpoenas are unduly burdensome. Essentially, Abbott (a company with nearly $30 billion in annual sales) argues that it is unduly burdensome to produce snapshot e-mails for a limited period of time for three specifically identified individuals out of a work force of approximately 72,000, even though Abbott has been required to maintain those emails for other litigation.

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Bluebook (online)
692 F. Supp. 2d 602, 2010 U.S. Dist. LEXIS 21947, 2010 WL 841258, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-subpoenas-vawd-2010.