Arnold v. Baxter Healthcare Corp.

609 F. Supp. 2d 712, 2009 U.S. Dist. LEXIS 16751, 2009 WL 1097325
CourtDistrict Court, N.D. Ohio
DecidedFebruary 17, 2009
DocketCase 1:08HC60025
StatusPublished
Cited by3 cases

This text of 609 F. Supp. 2d 712 (Arnold v. Baxter Healthcare Corp.) is published on Counsel Stack Legal Research, covering District Court, N.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Arnold v. Baxter Healthcare Corp., 609 F. Supp. 2d 712, 2009 U.S. Dist. LEXIS 16751, 2009 WL 1097325 (N.D. Ohio 2009).

Opinion

ORDER

JAMES G. CARR, Chief Judge.

This is a case in which plaintiffs, Elizabeth and Patrick Arnold, originally filed state-law claims against defendant Baxter Healthcare Corporation [Baxter] in the Circuit Court of Cook County, Illinois. The Arnolds seek damages for injuries allegedly caused by ingestion of Heparin, a drug manufactured and sold by Baxter. Asserting that plaintiffs’ complaint raises substantial federal questions, Baxter removed the case to the United States District Court for the Northern District of Illinois. That court, in turn, transferred the case in accordance with reference of pending federal Heparin cases pursuant to *714 an order entered in In re Heparin, MDL No. 1953.

Pending is plaintiffs’ motion to remand and for an award of costs and attorney fees. [Doc. 15]. The parties do not dispute the fact that they are not diverse. Baxter contends, in response to the motion to remand, that overriding and unavoidable issues of federal law under the Food, Drug and Cosmetic Act [FDCA], 21 U.S.C. § 301 et seq., which this court necessarily will have to decide, justify keeping the case in federal court. Baxter adds that the court will have to judge the adequacy of the Food and Drug Administration’s [FDA] actions and procedures. The Arnolds disagree, pointing out that they seek no relief under any federally-based cause of action.

For the reasons discussed below, the Arnolds’ motion to remand shall be granted, but I shall overrule their request for costs and attorney fees.

Standard of Review

After removal, plaintiffs may bring a motion to remand to state court under 28 U.S.C. § lUI(c), which states,

A motion to remand the case on the basis of any defect other than lack of subject matter jurisdiction must be made within 30 days after the filing of the notice of removal under section 1446(a). If at any time before final judgment it appears that the district court lacks subject matter jurisdiction, the case shall be remanded. An order remanding the ease may require payment of just costs and any actual expenses, including attorney fees, incurred as a result of the removal. A certified copy of the order of remand shall be mailed by the clerk to the clerk of the State court. The State court may thereupon proceed with such case.

Discussion

I must grant the Arnolds’ motion to remand to state court if I find that no federal question jurisdiction exists over their claims. Caterpillar Inc. v. Williams, 482 U.S. 386, 392, 107 S.Ct. 2425, 96 L.Ed.2d 318 (1987) (“[A]bsent diversity of citizenship, federal question jurisdiction is required” for proper removal to federal court).

Section 1331 establishes federal question jurisdiction. It states that “the district courts shall have original jurisdiction of all civil actions arising under the Constitution, laws, or treaties of the United States.” I must look to the face of the Arnolds’ well-pleaded complaint to see if their claims arise under federal law. Louisville & Nashville R.R. Co. v. Mottley, 211 U.S. 149, 152, 29 S.Ct. 42, 53 L.Ed. 126 (1908).

A case “arises under” federal law when “a well-pleaded complaint establishes either that federal law creates the cause of action or that the plaintiffs right to relief necessarily depends on resolution of a substantial question of federal law.” Empire Healthchoice Assur., Inc. v. McVeigh, 547 U.S. 677, 689-90, 126 S.Ct. 2121, 165 L.Ed.2d 131 (2006) (citation omitted). Defendant’s arguments or counterclaims cannot provide the basis for federal question jurisdiction. See, e.g., Holmes Group, Inc. v. Vornado Air Circulation Systems, Inc., 535 U.S. 826, 831, 122 S.Ct. 1889, 153 L.Ed.2d 13 (2002).

Federal question jurisdiction lies over state-law claims when “a state-law claim necessarily raise[s] a stated federal issue, actually disputed and substantial, which a federal forum may entertain without disturbing any eongressionally approved balance of federal and state judicial responsibilities.” Grable & Sons Metal Products, Inc. v. Darue Engineering & Manufacturing, 545 U.S. 308, 314, 125 S.Ct. 2363, 162 L.Ed.2d 257 (2005).

*715 I must therefore determine whether the Arnolds’ state-law claims 1) necessarily raise a stated federal issue; 2) whether the federal issues are actually disputed and substantial; and 3) whether a federal forum may entertain, the claims without disturbing any congressionally approved balance of federal and state judicial responsibilities. Based on my analysis of these requirements, I find that federal question jurisdiction cannot lie over the Arnolds’ claims.

1. The Arnolds’ Claims do Not Necessarily Raise a Federal Issue

Baxter argues that the Arnolds’ complaint challenges determinations made by the FDA and the adequacy of the federal regulatory process governing the manufacture and sale of prescription drugs. According to Baxter, the claims will require the court to interpret and apply federal law and determine the propriety of Baxter’s conduct in light of that law.

While Baxter contends all of plaintiffs’ claims raise substantial federal law issues, it points to only two allegations to support this argument: 1) Paragraph 7(d) of the Arnolds’ complaint, which alleges Baxter was negligent in failing to “comply with all statutes, laws, regulations, and safety codes pertaining to the manufacture, production, distribution, storage, and sale of Heparin;” [Doc. 1, Exh. A] and (2) Paragraph 7(i), which alleges Baxter was negligent in failing “to exercise reasonable care in acquiring the ingredients for Heparin only from producers and suppliers that had undergone proper inspection and evaluation, including, but not limited to, inspection and evaluation by the FDA.” Id.

The allegation that Baxter failed to comply with all statutes, laws and regulations regarding the manufacture and sale of Heparin is “federal in nature,” according to Baxter, because it implicates federal law. Baxter also posits that the allegation that it “failed to exercise reasonable care in acquiring the ingredients for Heparin” requires the court to determine “whether producers and suppliers at issue were properly FDA-approved” and such a determination would require “resolution of federal law.” [Doc. 1]. Finally, Baxter maintains that by holding it liable for Heparin administered to Patrick Arnold, the Arnolds challenge “the adequacy of the FDA procedures with which Baxter complied.” Id.

Baxter’s arguments fail to establish that the Arnolds’ claims necessarily raise a federal issue.

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Cite This Page — Counsel Stack

Bluebook (online)
609 F. Supp. 2d 712, 2009 U.S. Dist. LEXIS 16751, 2009 WL 1097325, Counsel Stack Legal Research, https://law.counselstack.com/opinion/arnold-v-baxter-healthcare-corp-ohnd-2009.