Luckey v. Baxter Healthcare Corp.

2 F. Supp. 2d 1034, 1998 WL 199051
CourtDistrict Court, N.D. Illinois
DecidedJune 19, 1998
Docket95 C 509
StatusPublished
Cited by34 cases

This text of 2 F. Supp. 2d 1034 (Luckey v. Baxter Healthcare Corp.) 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
Luckey v. Baxter Healthcare Corp., 2 F. Supp. 2d 1034, 1998 WL 199051 (N.D. Ill. 1998).

Opinion

MEMORANDUM OPINION AND ORDER

CASTILLO, District Judge.

Relator Joan Luckey, a former technician at the laboratories of defendant Baxter Healthcare Corporation (“Baxter”), brings this action on behalf of the United States pursuant to the qui tam provision of the False Claims Act (“FCA”), 31 U.S.C. § 3730(h). Count I of the complaint alleges that Baxter made false claims to the United States by (1) misrepresenting its testing of *1037 plasma and plasma based therapies was “adequate and effective”; and (2) misrepresenting compliance with federal regulations, in violation of 31 U.S.C. § 3729(a)(1). In Count II, Luckey alleges that Baxter wrongfully terminated her employment in retaliation for her pursuit of and investigation into Baxter’s allegedly false claims, in violation of the anti-retaliatory discharge provision of the FCA, 31 U.S.C. § 3730(h).

The United States has declined to intervene in this action pursuant to 31 U.S.C. § 3730(b)(4)(B). Luckey, however, continues to litigate these claims as the Relator under the qui tarn provisions of the FCA. Currently before the Court is Baxter’s motion for summary judgment on all counts of Luckey’s amended qui tam complaint. Baxter argues that Count I of Luckey’s complaint fails as a matter of law because Luckey has not submitted evidence demonstrating that Baxter knowingly lied to the government to procure a benefit. Baxter similarly characterizes Count II as baseless, contending that the evidence shows that Luckey was terminated for harassing her coworkers and other inappropriate behavior. For the following reasons, Baxter’s motion for summary judgment is granted in its entirety.

RELEVANT FACTS 1

1. Baxter’s Plasma Testing

Baxter is one of the world’s largest producers of plasma products. Baxter, through its subsidiaries, sells plasma products to hospitals, clinics, health maintenance organizations, doctors’ offices, and other medical facilities. Baxter’s customers include Medicare, Medicaid, Veterans Hospitals, and other hospitals receiving federal subsidies.

Baxter’s plasma products are produced from plasma that is collected from paid members of the general public at donor centers. Plasma is a primary component of human blood and can potentially carry bacterial and viral contaminants, including HIV 1, HIV 2, Hepatitis B, Hepatitis C, Syphilis, and Cre-utzfeldt-Jakob disease. Prior to incorporating donor-center samples into its plasma products, Baxter sends donated plasma to its subsidiary, Baxter Biotechnology Screening Laboratory (“Baxter labs”), for product testing. Baxter labs conducts several tests to determine whether the donated plasma contains harmful contaminants.

The routine testing protocol includes the Alanine Amino Transfer test (“ALT”), which Baxter labs uses to determine, among other things, the donor’s liver quality. Samples yielding low ALT results are subject to additional testing to make certain the samples actually consist of plasma. Baxter became aware that some donor centers were using inadequate plasma collection procedures that failed to prevent saline from mixing with plasma. The presence of excessive saline could impair the screening tests’ ability to detect the existence of viral contaminants, causing “false negative results”.

Prior to 1995, Baxter labs utilized the Col- or Inspection Test to evaluate the quality of suspect samples. Under this approach, technicians were directed to inform their supervisors when samples yielded a low ALT result. The supervisor then inspected the sample to determine whether it was clear, cloudy, or colorless. If the sample appeared colorless, the supervisor would order a Total Protein Test to determine whether proteins were present in the samples. The absence of pro *1038 teins indicated that the sample could be saline diluted, and the sample would be rejected.

Baxter issued Protocol 93-019 to combat the saline problem in the spring of 1998. Protocol 93-019 conceded that samples improperly diluted with saline were presented for testing at Baxter labs. This protocol instructed workers in Baxter labs’ customer operations division to examine and evaluate the samples when they first arrive at Baxter, prior to testing. Bychowski Dep. at 153. Baxter subsequently adopted Protocol 94-025 in the spring of 1994 to provide a method to test samples suspected of being diluted with saline. Bychowski Dep. at 163. This protocol enabled technicians to test suspect plasma samples for total proteins. Id. at 165. Following an audit by the Federal Food and Drug Administration, Baxter was directed to and did adopt a protocol requiring technicians to perform the Total Protein Test on all plasma samples yielding a low ALT result, regardless of whether the samples were colorless.

Once a sample is approved at Baxter labs, Baxter forwards the sample to another Baxter subsidiary, the Hyland Division of Baxter Healthcare (“Hyland”). Hyland pools plasma from various testing centers to create its plasma products. Hyland’s combined pool contains approximately 20,000 liters of plasma.

2. Joan Luckey’s Employment with Baxter

Luckey began working at Baxter labs as a Lab Technician III in December, 1991. Baxter places all new employees on probationary status for three months, and Luckey was no exception to the rule. As a probationary employee, Luckey was responsible for reviewing data and checking test results for accuracy. Charmaine Bychowski, Luckey’s supervisor, evaluated Luckey’s performance after 30, 60, and 90 days. 2 Luckey received “acceptable” ratings — the highest rating available — in all categories evaluated on her 30 and 60 day reviews. In Luckey’s 90 day review, however, Bychowski downgraded her assessment of the quality of Luckey’s work to “marginal”, noting that “[Luckey] released a bundle ... without first submitting it for verification testing. Joan has a fair number of ‘missing signature/initials’ type of documentation errors.” Pl.’s Facts Ex. R. Baxter decided that “in an effort to raise [Luekey’s] quality to acceptable, the probationary period will be extended to ten days.” Id.

In the Spring of 1992, technician Candy Johnson tested and retested a plasma sample, achieving invalid results. Luckey examined the sample, noted that it looked like water or saline, and informed Bychowski of her discovery. Luckey suggested running a Total Protein Test to determine whether the sample was actually plasma. Luckey Dep. at 18. Luckey alleges that Bychowski responded that “we don’t look” and “we don’t ask questions.” Luckey Dep. at 14. Luckey contends that she had continuing discussions with Bychowski regarding the saline incident and the need to use the Total Protein Test consistently. Id. at 24.

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Bluebook (online)
2 F. Supp. 2d 1034, 1998 WL 199051, Counsel Stack Legal Research, https://law.counselstack.com/opinion/luckey-v-baxter-healthcare-corp-ilnd-1998.