Doe v. Armour Pharmaceutical Co.

837 F. Supp. 178, 1993 U.S. Dist. LEXIS 13313, 1993 WL 406539
CourtDistrict Court, E.D. Louisiana
DecidedSeptember 21, 1993
DocketCiv. A. 93-0514, 93-1474, 93-1475, 93-1476, 93-2069, 93-2142, 93-2331 and 93-2425
StatusPublished
Cited by4 cases

This text of 837 F. Supp. 178 (Doe v. Armour Pharmaceutical Co.) is published on Counsel Stack Legal Research, covering District Court, E.D. Louisiana primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Doe v. Armour Pharmaceutical Co., 837 F. Supp. 178, 1993 U.S. Dist. LEXIS 13313, 1993 WL 406539 (E.D. La. 1993).

Opinion

ORDER AND REASONS

MENTZ, District Judge.

This matter is before the Court on motions to remand to state court or alternatively to stay proceedings filed by plaintiffs in each of several lawsuits involving hemophiliacs infected with the HIV virus. The Court took these motions under submission without oral argument and now GRANTS the motions to remand as follows.

I. THE PARTIES

Each of these eight lawsuits 1 has been brought on behalf of hemophiliacs and their relatives against Tulane Medical School 2 (Tulane), Dr. W. Abe Andes (Dr. Andes), and a varying combination of three alleged manufacturers of a blood clotting factor used to treat hemophilia.

The hemophiliacs are children and are citizens of Louisiana 3 , as are their relatives, who are bringing these suits on their behalf. The hemophiliacs and their relatives shall be referred to collectively as the plaintiffs.

Dr. Andes has allegedly been a citizen of North Carolina since August 1, 1992. However, at the time of the actions under consideration 4 , Dr. Andes was living in Louisiana and was an employee of Tulane, which is a non-profit Louisiana corporation. Tulane and Dr. Andes shall be referred to collective *181 ly on occasion as the medical defendants. Both Dr. Andes and Tulane qualify as health care providers under the Louisiana Medical Malpractice Act.

The three alleged “manufacturers” 5 of the blood clotting factors are Armour Pharmaceutical Company (Armour), Miles Inc., 6 (Miles), and Alpha Therapeutics (Alpha), and shall be referred to collectively as defendant manufacturers. The blood clotting factors are Factorate and Factor VIII, which are processed by Armour, Koate, a product of Miles, and Profilate, of ATI.

Although the defendant manufacturers appear in different combinations in these eases, these variations have no bearing on the Court’s ruling. It is relevant, however, that none of the defendant manufacturers is domiciled in the State of Louisiana nor has a principal place of business within Louisiana.

II. THE FACTUAL BACKGROUND AND PROCEDURAL POSTURE

From 1979 through at least 1991, Tulane operated a clinic for the treatment of individuals who suffered from hemophilia, including plaintiffs. The clinic was known as the Louisiana Comprehensive Hemophilia Care Program and had as its director Dr. Andes, who was also the treating physician for the hemophiliacs in this case.

Plaintiffs allege the hemophiliacs were infected with the HIV virus, the causative agent of the condition known as AIDS, through the intravenous use of blood clotting factors prescribed by Dr. Andes in their treatment. Employing various negligence theories, plaintiffs allege that Dr. Andes knew or should have known the dangers inherent in this treatment, that he failed to warn plaintiffs whose consent was thus uninformed, that he failed to utilize or advise of alternative medical techniques that were safer, that he misrepresented the risks involved in the use of the blood clotting factors, and that when these risks became obvious, he threatened to withhold access to any treatment if plaintiffs were to pursue legal remedies.

Plaintiffs further allege that Tulane, as the direct employer of Dr. Andes, is responsible for his actions under the theory of responde-at superior; and that Armour and Miles compensated Dr. Andes and were thus also responsible for his actions as their agent. Plaintiffs have additional negligence and breach of implied warranty of fitness or merchantability claims against Tulane and the defendant manufacturers.

All eight of the cases before this Court were originally filed in the Civil District Court for the Parish of Orleans and timely removed to federal court for the Eastern District of Louisiana.

Similar cases pending in Civil District Court of the Parish of Orleans have been consolidated in Division “L”, presided over by Judge Max N. Tobias, Jr.

At present, the case entitled Gary W. Cross, et al. v. Cutter Biological, et al., # 91-9617 (Cross), is set for trial before Judge Tobias on October 5, 1993. Previously removed to federal court, Cross was likewise remanded to state court by Judge Peter Beer of the Eastern District of Louisiana, based on a ruling by Judge Martin Feldman in another related ease, Doe v. Cutter Biological, 774 F.Supp. 1001 (E.D.La.1991).

In the instant case defendants vigorously argue that plaintiffs have fraudulently joined Tulane and Dr. Andes in an attempt to avoid federal jurisdiction. Contending the Doe decision was incorrect, defendants 7 go so far as to say,

No judge on the bench of the United States District Court for the Eastern District of Louisiana has addressed all the issues raised by defendants in this case. *182 The plaintiffs statement that “The precise argument now presented by Cutter has previously been raised in fourteen separate proceedings in the Eastern District of Louisiana” is completely untrue.

Due to the emotional upheaval surrounding the circumstances of children suffering from AIDS, and equally important, due to the need to fill some of the interstices of Judge Feldman’s ruling, the Court takes this occasion to amplify, though nevertheless to embrace the decision in Doe.

III. THE DEFENDANTS’ ARGUMENTS

The guideposts for removal were succinctly laid out in Hayden v. Phillips Petroleum Co., 788 F.Supp. 285 (E.D.La.1992).

The burden is on the defendants, as the removing parties, to establish the existence of federal jurisdiction. Dodson v. Spiliada Maritime Corp., 951 F.2d 40 (5th Cir.1992). To prove fraudulent joinder, the defendants must demonstrate that the plaintiffs have no possible cause of action against the non-diverse defendant. B., Inc. v. Miller Brewing Co., 663 F.2d 545 (5th Cir.1981). All ambiguities in the controlling law and all disputed questions of fact are to be resolved in favor of the non-removing party. Carriere v. Sears, Roebuck & Co., 893 F.2d 98, 100 (5th Cir.), cert. denied, 498 U.S. 817, 111 S.Ct. 60, 112 L.Ed.2d 35 (1990).

It is within this framework that defendants’ arguments must be addressed.

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Englande v. SMITHKLINE
206 F. Supp. 2d 815 (E.D. Louisiana, 2002)
Johnson v. Scimed, Inc.
92 F. Supp. 2d 587 (W.D. Louisiana, 2000)
Gandy v. Crompton
55 F. Supp. 2d 593 (S.D. Mississippi, 1999)
Horton Ex Rel. Horton v. Scripto-Tokai Corp.
878 F. Supp. 902 (S.D. Mississippi, 1995)

Cite This Page — Counsel Stack

Bluebook (online)
837 F. Supp. 178, 1993 U.S. Dist. LEXIS 13313, 1993 WL 406539, Counsel Stack Legal Research, https://law.counselstack.com/opinion/doe-v-armour-pharmaceutical-co-laed-1993.