West v. Bayer Healthcare Pharmaceuticals, Inc.

CourtDistrict Court, District of Columbia
DecidedFebruary 1, 2018
DocketCivil Action No. 2015-1053
StatusPublished

This text of West v. Bayer Healthcare Pharmaceuticals, Inc. (West v. Bayer Healthcare Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
West v. Bayer Healthcare Pharmaceuticals, Inc., (D.D.C. 2018).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

WILLIAM PRESTON WEST, JR., et al., Plaintiffs,

v. Civil No. 15-1053 (CKK) BAYER HEALTHCARE PHARMACEUTICALS INC., et al., Defendants.

MEMORANDUM OPINION (February 1, 2018)

Plaintiff William Preston West, Jr. alleges that he contracted a severe bacterial infection

after using a contaminated alcohol prep pad that was packaged with an injectable medicine

produced by Defendant Bayer HealthCare Pharmaceuticals, Inc. (“Bayer”). Plaintiff and his

wife, Carolyn Gleason, have filed this lawsuit against Bayer, asserting causes of action for

negligence, gross negligence, failure to recall, failure to warn or instruct, strict liability, breach of

implied warranty, negligence per se, punitive damages and loss of consortium. 1 Presently

pending before the Court are Defendant Bayer’s [124] Motion to Exclude the Expert Opinions of

Paul Auwaerter, M.D. and Mark Abbruzzese, M.D., and [125] Motion for Summary Judgment.

Upon consideration of the pleadings, 2 the relevant legal authorities, and the record for the

1 In addition to his claims against Bayer, Plaintiff West also originally asserted a claim against the manufacturers of the alcohol prep pads, Triad Group, Inc., Triad Pharmaceuticals, Inc., and H&P Industries, Inc. (collectively, “Triad”). That claim was resolved through Triad’s bankruptcy. The current action involves only Plaintiffs’ claims against Bayer. 2 The Court’s analysis has focused on the following documents: • Def.’s Mot. to Exclude the Expert Opinions of Paul Auwaerter, M.D. and Mark Abbruzzese, M.D., ECF No. 124 (“Def.’s Mot. to Exclude”); • Def.’s Mot. for Summary Judgment, ECF No. 125 (“Def.’s MSJ”); • Pls.’ Opp’n to Def.’s Mot. for Summary Judgment, ECF No. 126 (“Pls.’ Opp’n to MSJ”); 1 purposes of these motions, the Court will DENY Defendant’s Motion to Exclude, and GRANT-

IN-PART and DENY-IN-PART Defendant’s Motion for Summary Judgment.

Specifically, the Court concludes that the opinions of Plaintiffs’ experts are admissible

because they have an adequate factual basis and are sufficiently reliable. Defendant’s critiques

of those opinions bear on their weight, and can be explored through cross-examination, but they

do not render those opinions inadmissible. Largely because the Court will allow Plaintiffs to

present this expert testimony, summary judgment for Defendant is not appropriate on Plaintiff

West’s substantive claims. Summary judgment is also not appropriate on Plaintiff Gleason’s loss

of consortium claim. All parties agree that this claim is derivative of Plaintiff West’s substantive

claims, which are not being summarily adjudicated. Finally, the Court will grant Defendant

summary judgment on Plaintiff’s gross negligence and punitive damages claims, because

Plaintiffs consent to the dismissal of those claims.

I. BACKGROUND

Although the record before the Court is quite voluminous, the facts of this case are

actually fairly straightforward. Plaintiff William P. West has Multiple Sclerosis (“MS”).

Plaintiff was prescribed an injectable medicine called Betaseron to treat his MS. Defendant

Bayer produces Betaseron. The Betaseron injection kits distributed by Bayer contain alcohol

• Pls.’ Opp’n to Def.’s Mot. to Exclude the Expert Opinions of Paul Auwaerter, M.D. and Mark Abbruzzese, ECF No. 127 (“Pls.’ Opp’n to Mot. to Exclude”); • Def.’s Reply in Support of Mot. to Exclude the Expert Opinions of Paul Auwaerter, M.D. and Mark Abbruzzese, M.D., ECF No. 128 (“Def.’s Reply in Support of Mot. to Exclude”); • Def.’s Reply in Support of Mot. for Summary Judgment, ECF No. 129 (“Def.’s Reply in Support of MSJ”). The Court has also reviewed all of the evidentiary material attached to these pleadings. In an exercise of its discretion, the Court finds that holding oral argument in this action would not be of assistance in rendering a decision. See LCvR 7(f). 2 prep pads manufactured by Triad Group, Inc., Triad Pharmaceuticals, Inc., and H&P Industries,

Inc., (collectively, “Triad”). Plaintiff had been using these kits for several years prior to 2010. 3

On the evening of December 29, 2010, after using the provided Triad alcohol prep pads,

Plaintiff self-administered his Bayer Betaseron injection. Immediately thereafter, he developed

cellulitis in his abdominal wall. Plaintiff West had to be hospitalized for an extended period.

During his hospitalization, Plaintiff had a number of cultures taken—some before and some after

Plaintiff began receiving antibiotics—but none of those cultures definitively identified the

specific bacterial source of Plaintiff’s illness.

While in the hospital, Plaintiff received an e-mail from Bayer. The e-mail stated that

“Bayer HealthCare Pharmaceuticals has become aware of a broad United States market recall of

alcohol prep pads . . . manufactured by the Triad Group . . . due to potential contamination of

these products with the bacteria, Bacillus cereus [“B. cereus”], that could lead to life-threatening

infections.” Pls.’ Ex. 1, ECF No. 127-3, at 1. 4 The recall warned that “Triad alcohol prep pads

packaged for use in the U.S. with Betaseron should not be used by patients.” Id. As one might

expect, Plaintiff immediately told his treating physician about this potential source of his illness.

Plaintiffs allege in this lawsuit that Plaintiff West’s abdominal wall cellulitis was the

result of an infection caused by B. cereus bacteria that was present on the Triad alcohol pads in

3 Defendant’s Reply in Support of its Motion for Summary Judgment is largely dedicated to arguing that Plaintiffs’ Statement of Genuine Issues of Material Fact does not comply with Local Civil Rule 7(h). The Court need not engage in an analysis of whether or not Plaintiffs’ Statement was proper. The Court has based the conclusions in this Memorandum Opinion on a careful review of the record and the parties’ briefs, and any dispute about the format of the parties’ statements of fact did not affect those conclusions. 4 Many of the exhibits to Plaintiffs’ two opposition briefs (one in opposition to Defendant’s Motion to Exclude, and the other in opposition to Defendant’s Motion for Summary Judgment) are the same. Citations to Plaintiffs’ exhibits in this Memorandum Opinion refer to the exhibits attached to Plaintiffs’ Opposition to Defendant’s Motion to Exclude, ECF No. 127. 3 the Betaseron injection kit that he used on December 29, 2010. Plaintiffs have proffered two

expert witnesses that agree that this is the most likely explanation for Plaintiff’s illness. Dr.

Mark R. Abbruzzese is an infectious disease specialist licensed to practice in the District of

Columbia. See Pls.’ Ex. 2 (Pls.’ Preliminary Expert Witness Designations), ECF No. 127-4, at 5.

Dr. Paul G. Auwaerter is a board-certified internal medicine and infectious disease doctor who

serves as the Clinical Director of the Division of Infectious Diseases at Johns Hopkins Medicine

and is a professor of medicine at Johns Hopkins University School of Medicine. Id. at 8. Both

experts have lengthy, relevant and impressive backgrounds relating to infectious diseases. See

Pls.’ Ex. 5 (Abbruzzese Curriculum Vitae), ECF No. 127-7; Pls.’ Ex. 6 (Auwaerter Curriculum

Vitae), ECF No. 127-8.

Dr. Abbruzzese treated Plaintiff during and after his hospitalization, and is expected to

testify that, based on his expertise with infectious diseases, and “Plaintiff’s clinical history and

presentation, including the nature and severity of his infection and its sequelae . . . Plaintiff’s

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