Jirak v. Abbott Laboratories, Inc.

716 F. Supp. 2d 740, 16 Wage & Hour Cas.2d (BNA) 682, 2010 U.S. Dist. LEXIS 58804, 2010 WL 2331098
CourtDistrict Court, N.D. Illinois
DecidedJune 10, 2010
Docket07 C 3626
StatusPublished
Cited by2 cases

This text of 716 F. Supp. 2d 740 (Jirak v. Abbott Laboratories, Inc.) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Jirak v. Abbott Laboratories, Inc., 716 F. Supp. 2d 740, 16 Wage & Hour Cas.2d (BNA) 682, 2010 U.S. Dist. LEXIS 58804, 2010 WL 2331098 (N.D. Ill. 2010).

Opinion

MEMORANDUM OPINION AND ORDER

RUBEN CASTILLO, District Judge.

James Jirak (“Jirak”) and Robert Pedersen (“Pedersen”) bring this putative class action, on behalf of themselves and all others similarly situated, (collectively “Plaintiffs”) against Abbott Laboratories, Inc. (“Defendant”) for alleged violations of the overtime provisions of the Fair Labor Standards Act, 29 U.S.C. § 201 et seq. (“FLSA”). (R. 49, First Am. Compl.) Presently before the Court are Plaintiffs’ *742 (R. 143) and Defendant’s (R. 147) cross-motions for summary judgment. For the reasons stated below, Plaintiffs’ motion is granted and Defendant’s motion is denied.

RELEVANT FACTS 1

Defendant is a global, broad-based health care company headquartered in Illinois. (R. 144, Pis.’ Facts ¶ 1.) Plaintiffs are current and former employees of Defendant that worked as Pharmaceutical Representatives (“Representatives”). (Id. ¶ 2.) Representatives had the core duties of “generating market share and market share growth for assigned professional pharmaceutical products” and “mak[ing] selling presentations to physicians and other health care professionals.” (R. 149, Def.’s Facts ¶ 8.) Representatives, however, did not promote Defendant’s products directly to patients or end-users. (R. 144, Pis.’ Facts ¶ 53.)

Representatives received initial training from Defendant on science and selling skills. (R. 149, Def.’s Facts ¶ 10.) This included training on product and competitor product information as well as selling techniques and techniques to determine the physician’s needs. (Id. ¶¶ 11, 13-14.) After the initial period of training, Representatives received training to continue to develop these skills and were also encouraged to participate in sales training outside of the company. (Id. ¶¶ 16,19.)

Representatives were evaluated on their ability to utilize their training in the field. (Id. ¶ 10.) During “calls” or visits to health care providers, Defendant expected Representatives to adhere to company policies and federal and state laws that govern the pharmaceutical industry. (R. 144, Pis.’ Facts ¶ 11.) Their evaluations were based on job responsibilities that included “selling to customers” and “coordinating] sales efforts.” (R. 149, Def.’s Facts ¶20.) Defendant provided each Representative with a “call list” specifying the physicians in their assigned territory that they were to present information about Defendant’s products. (R. 144, Pis.’ Facts ¶¶ 8, 10.) Defendant ranked the physicians on the “call list” and Representatives were expected to call on the higher-ranked physicians with more frequency than others. 2 (Id. ¶¶ 39-40.) Each Representative was also supplied with a laptop computer to enter “call notes” describing what they did on a particular sales call. (Id. ¶ 11.) District Managers (“DMs”) had access to these “call notes” to ensure that Representatives were following appropriate procedure. (Id.) DMs could also conduct “ride alongs” to monitor Representatives during their calls. (Id.)

Representatives were expected to deliver “core messages” created by Defendant’s marketing department about the products to health care providers. (Id. ¶¶ 4-5, 41.) Although Plaintiffs contend that Representatives “could not deviate” from these messages, the record illustrates that Representatives were not provided “transcripts of communications to be repeated verbatim.” (R. 144, Pis.’ Facts ¶4; R. 162, Def.’s Resp. Facts ¶ 4.) Rather, they were free to “weave” these “core messages” into “their overall product conversations with doctors.” (Id.)

*743 To assist with “core message” delivery, Defendant’s marketing department provided “visual aids” and material that Representatives could use or distribute during them calls. (R. 144, Pis.’ Facts ¶¶ 6, 9.) The messaging and material was created under the supervision of Defendant’s medical, regulatory, and legal departments to ensure compliance with industry and company policy. 3 (R. 162, Def.’s Resp. Facts ¶ 6.) Although Representatives were “prohibited” from using aids that had not been approved by Defendant, they did have discretion to decide which, if any, materials to use during a particular call. (Id. ¶ 9.) Representatives were evaluated on their ability to “consistently giv[e] a logical, reasonable call-to-aetion/close on every sales call to drive product adoption and utilization.” (R. 149, Def.’s Facts ¶26.) “Closing,” however, did not create a contract or an enforceable commitment by the doctor to write a prescription for Defendant’s products. 4 (R. 144, Pis.’ Facts ¶ 19.)

Even if the targeted doctor wrote a prescription for the product and it was filled by a pharmacy, Defendant did not recognize income. (Id. ¶ 15.) Rather, Defendant recognized revenue when their “trade group” provided pharmaceutical products to wholesale and retail customers. (Id.) Eighty to ninety percent of the revenue recognized by Defendant came from sales to wholesalers. (Id.) The remaining ten to twenty percent, was from sales to managed care entities, VA hospitals, long-term care facilities, independent hospital, independent pharmacies, and other small entities. (Id.; R. 162, Def.’s Resp. Facts ¶ 15.) However, in addition to their base wages, Representatives were paid “incentive compensation” that was calculated, in part, based on prescriptions written in the Representatives’ assigned territory. (R. 149, Def.’s Facts ¶¶ 30-35.)

PROCEDURAL HISTORY

Jirak and Pedersen originally filed this action on June 28, 2007, and amended their complaint on November 27, 2007. (R. 1, Compl.; R. 49 First Am. Compl.) On February 1, 2008, Jirak and Pedersen moved for conditional certification of a class and approval of proposed notice to potential class members pursuant to Section 16(b) of the FLSA. (R. 54, Pis.’ Mot.) This Court granted the motion, in part, on July 22, 2008, 566 F.Supp.2d 845 (N.D.Ill.2008). (R. 64, Order.) In the July 22 Opinion, the Court rejected the notice proposed by Plaintiffs but authorized a revised notice plan on September 3, 2008. (Id.; R. 70, Min. Entry.)

On December 14, 2009, Plaintiffs and Defendant filed cross-motions for summary judgment focusing on whether Plaintiffs were exempt from the overtime requirements of the FLSA under either the outside sales or administrative exemptions. (R. 145, Pis.’ Mem. in Support of Summ. J. Mot. (“Pis.’ Mem.”); R. 147, Def.’s Summ. J. Mot.) On January 7, 2010, the Court granted Defendant’s motion to dismiss *744 Opt-in Plaintiffs who did not work for Defendant as Representatives during the limitations period. (R. 157, Min. Entry.) In addition, on March 2, 2010, the Court granted Defendant’s motion to dismiss OpNIn Plaintiffs who refused to participate in discovery. (R. 179, Min. Entry.)

LEGAL STANDARDS

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716 F. Supp. 2d 740, 16 Wage & Hour Cas.2d (BNA) 682, 2010 U.S. Dist. LEXIS 58804, 2010 WL 2331098, Counsel Stack Legal Research, https://law.counselstack.com/opinion/jirak-v-abbott-laboratories-inc-ilnd-2010.