TERESA J. JAMES, Magistrate Judge.
This matter is before the Court on Class Plaintiffs' Amended Motion to Compel Compliance with Subpoena Directed to Non-Party Humana, Inc. (ECF No. 292). Pursuant to Fed. R. Civ. P. 26 and 45, Class Plaintiffs seek an order requiring non-party Humana, Inc. to search for and produce documents responsive to Plaintiffs' subpoena served on December 11, 2017. Humana opposes the motion. As set forth below, the Court will grant Plaintiffs' motion.
On December 11, 2017, Plaintiffs served a Rule 45 subpoena on Humana. Under Rule 45(d)(2)(b), Humana's deadline for objections was 14 days after service of the subpoena.
Counsel continued to communicate, but as of the date Plaintiffs filed the instant motion, Humana had produced no responsive documents. On March 1, 2018, Humana produced 17 documents relating to six subpoena requests, with no indication whether additional documents exist that are responsive to those requests. Humana has not produced any documents in response to another six requests, nor has it indicated when it will do so.
The parties have engaged in extensive written and oral communication regarding the subpoena. Based on the parties' efforts, the Court finds they have complied with the requirements of D. Kan. R. 37.2.
Plaintiffs assert this Court has jurisdiction to decide this motion, while Humana contends the motion should be heard in the Western District of Kentucky, the district that includes the place for compliance. Regarding the merits, Plaintiffs contend all their requests are relevant and Humana should be compelled to produce responsive documents. Humana stands by its objections, arguing that collectively they demonstrate the subpoena imposes undue burden and expense on Humana.
In issuing a subpoena, a party must "take reasonable steps to avoid imposing undue burden or expense on a person subject to the subpoena."
Federal Rule of Civil Procedure 45 governs both motions to compel compliance with and motions to quash a subpoena served on a non-party.
"The scope of discovery under a subpoena is the same as party discovery permitted by Fed. R. Civ. P. 26."
Plaintiffs assert that as the MDL transferee court, this Court has jurisdiction to rule on their motion to compel. Humana disagrees and although it does not say so directly, hints that the authorities Plaintiffs cite are no longer good law after the 2013 amendment to Rule 45. Prior to the amendment, Rule 45 required that subpoenas issue from the district where compliance was required.
The language in Rule 45 which assigns enforcement to "the court for the district where compliance is required" refers only to orders quashing or modifying a subpoena.
However, the basis for ruling that an MDL transferee court has authority to rule on a motion to compel in this situation (where a Rule 45 subpoena is issued by the MDL court but compliance is sought in another district) is not Rule 45 or Rule 37. Instead, courts find authority in 28 U.S.C. § 1407, the statute authorizing the MDL Panel to transfer civil actions involving one or more common questions of fact for coordinated pretrial proceedings.
Although Humana does not object to any of the requests on the basis of relevancy, the Court finds it appropriate to examine the relevancy of the requests to afford Humana the heightened protection a non-party deserves. Construing relevancy broadly, as the standard directs, the Court finds Plaintiffs' document requests clearly encompass matters that bear on their claims in this case. This is an antitrust, civil RICO, and consumer-protection class action brought on behalf of those who purchased or used the EpiPen, an epinephrine auto-injector ("EAI"). The Complaint's allegations make relevant a number of topics for discovery, including the EAI market, EAI device coverage and formulary placement or exclusion, usage, claims, consumer costs, demand and competitive conditions, and EAI-related payments and costs along the distribution and pharmaceutical supply chain.
Given Plaintiffs' allegations, the Court finds relevant the categories of requests included in Plaintiffs' subpoena. As Plaintiffs describe their requests, they include: (i) rebate and formulary information, including agreements, communications and other deliberative materials relating to those agreements; and (ii) documents concerning consideration paid or received related to the marketing, distribution, or sale of any EAI Drug Device. See Ex. 1, Req. No. 1 (documents regarding rebate or incentive agreements); id., Req. No. 4 (consideration related to marketing, distribution or sale of EAI Drug Devices); id., Req. No. 7 (documents concerning agreements with EAI Drug Device Manufacturers regarding sale, reimbursement, formulary placement, etc.); and id., Req. No. 14 (decision or consideration to include or exclude any EAI Drug Device from formularies).
Having found the document requests facially relevant, the Court turns to Humana's objections.
Citing Rule 45's directive that courts must enforce the serving party's obligation to take "reasonable steps to avoid imposing undue burden or expense,"
Humana's objections to the individual requests are boilerplate; they state an objection without offering an explanation. In response to Humana's boilerplate objections, Plaintiffs point out that Humana recognizes the documents Plaintiffs seek are uniquely within Humana's possession or control.
The same applies to Humana's assertion that Plaintiffs' request for communications and deliberative materials are improper. Humana objects to Requests 1, 4, 7, and 14 as overbroad and unreasonable in scope. It offers no explanation for its boilerplate objections. Humana also argues the requests are not likely to lead to the discovery of admissible evidence.
"Whether a subpoena imposes an undue burden upon a respondent raises a case-specific inquiry. It turns on such factors as relevance, the need of the party for the documents, the breadth of the document request, the time period covered by it, the particularity with which the documents are described and the burden imposed."
As the Court has noted, the scope of discovery under a subpoena is the same as party discovery permitted by Rule 26.
Next, Humana objects that certain words and terms are vague and ambiguous, including "understanding," "potential demand," and "collectively or individually." Once again, these objections are boilerplate. The Court finds Humana's boilerplate objections lack support and do not adequately provide a basis for the Court to grant them.
Finally, Humana objects to producing documents that Plaintiffs can obtain from Defendants. In addition to this being an improper objection to a subpoena, the Court rejects Humana's unsupported assertion that the subpoena calls for discovery Plaintiffs can otherwise obtain. To the extent Plaintiffs seek Humana's internal communications and deliberations, as well as documents, agreements, and communications with non-party manufacturers, there would be no duplication. In addition, Humana is not in a position to know what other parties will produce, nor whether a particular document may differ in version or have additions or omissions when coming from two different sources.
The Court overrules Humana's objections.
The Court has reviewed the individual requests to determine relevancy based on the claims and defenses to this action, and to assess whether Plaintiffs have taken reasonable steps to avoid imposing undue burden or expense as required by Rule 45(d)(1).
The Court finds the relevant time period (modified by Plaintiffs at Humana's request) of January 1, 2009 to the present to be reasonable, as it begins two years after Mylan acquired the rights to EpiPen that it continues to hold. The Court finds reasonable Plaintiffs' offer to limit the scope of the subpoena to documents uniquely within Humana's possession or control, provide Humana with a specific list of data fields to assist in data production, narrow the relevant time period at Humana's request, and make suggestions where responsive documents may likely be located. The Court will enforce the subpoena.