Opinion

Baker v. E.I. Dupont De Nemours and Co.

Court
District Court, N.D. New York
Filed
Sep 19, 2024
Cited by
0 cases
Authority
More cited than 31.7%

The opinion

UNITED STATES DISTRICT COURT

NORTHERN DISTRICT OF NEW YORK

MICHELE BAKER, et al.,

Plaintiffs,

V. 1:16-CV-917

(LEK/DJS)

SAINT-GOBAIN PERFORMANCE

PLASTICS CORP., et al.,

Defendants.

DANIEL J. STEWART

United States Magistrate Judge

MEMORANDUM-DECISION AND ORDER

Presently pending before the Court is Defendant’s Motion to exclude proposed

expert testimony by Jamie DeWitt regarding DuPont’s assessment of PFOA risks. Dkt.

No. 402. Plaintiffs seek to have DeWitt testify to the following opinions:

¢ The information DuPont and 3M possessed in the 1980s regarding

potential adverse risk to human health from PFOA exposure required that

they conduct a thorough and comprehensive human health risk assessment;

* The risk assessment proposal and goals and plans of the C-8 Project in the

late 1990s provided a belated, but appropriate, plan to assess the risk PFOA

exposure posed to human health in accordance with generally accepted

methodology in the field as published in EPA’s guidelines for performing

such a risk assessment;

¢ Nothing provided to me for this review, including the articles, internal

studies, memos, and emails discussed with Dr. Frame at his deposition

demonstrate that DuPont ever completed an appropriate human risk

assessment for PFOA exposure consistent [with] generally recognized and

accepted methodology as was contemplated under the C-8 Program.

* A properly conducted human health risk assessment would have provided

DuPont with valuable additional information about the risks to human health

posed by PFOA exposure which then could have been shared with customers

and others likely to be exposed to PFOA from DuPont’s products to warn

them to avoid exposure;

¢ In fact, if DuPont had conducted the human health risk assessment as

outlined in their C-8 Project, it may also have led to a decision to remove

PFOA and related compounds from their products more than a decade before

PFOA use was actually discontinued; and

* It is my opinion, based upon my experience and the documents I reviewed,

that the risk assessment proposed for the C-8 Project should have been

performed following appropriate guidelines and protocols, and that health

agencies needed to be informed and involved as early as the late 1970s when

human exposures and initial animal tests demonstrated results of concern to

DuPont and 3M scientists and other employees aware of the results.

Dkt. No. 402-2, DeWitt Report at pp. 9-10. DuPont seeks to exclude testimony from

Dr. DeWitt on three specific aspects of her opinion. As set forth in its Motion, DuPont

objects to the following:

* First, DeWitt opines that, as early as the late 1970s, human exposures and

initial animal tests known to DuPont obligated it to “inform and involve”

health agencies regarding the human health risks of PFOA.

* Second, DeWitt asserts that, although DuPont possessed sufficient

information to do so, it never completed and produced an “appropriate” final,

written report of human health risk assessment for PFOA exposure in the late

1990s/early 2000s as part of its “C-8 PACE Team” effort.

*Third, DeWitt claims that if DuPont had conducted a “proper” human

health risk assessment in the late 1990s or early 2000s and prepared a final

“report” using EPA guidelines, it would have uncovered information that

may have led DuPont to (1) issue additional or different warnings regarding

PFOA exposure and (11) eliminate sooner the use of PFOA as a surfactant in

certain products. !

Dkt. No. 402-15, Def.’s Mem. of Law at pp. 4-5 (citations omitted). Defendant seeks

to exclude the opinions on multiple grounds, including DeWitt’s lack of qualifications

offer her opinions, lack of proper basis for the opinions, the application of

inappropriate standards in reaching the opinion, and the speculative nature of the

opinions being offered. See generally Def.’s Mem. of Law. Plaintiffs oppose the

Motion. Dkt. No. 416, Pl.’s Mem. of Law.” Defendant has filed a Reply. Dkt. No. 429.

Following oral argument and for the reasons set out below, the Motion is granted in part

and denied in part.

I. LEGAL STANDARD

Under FED. R. EVID. 702:

A witness who is qualified as an expert by knowledge, skill, experience,

training, or education may testify in the form of an opinion or otherwise if

the proponent demonstrates to the court that it is more likely than not that:

(a) the expert’s scientific, technical, or other specialized knowledge will help

the trier of fact to understand the evidence or to determine a fact in issue;

(b) the testimony is based on sufficient facts or data;

(c) the testimony is the product of reliable principles and methods; and

' These opinions will be referred to throughout this Decision as the first, second, and third opinions.

? Plaintiffs, however, have stated their intention to withdraw the portion of Dr. De Witt’s first opinion, regarding

the need to notify health officials, Pls.” Mem. of Law at p. 8 n.4, and so the Court need not address DuPont’s

objections that opinion.

(d) the expert’s opinion reflects a reliable application of the principles and

methods to the facts of the case.

“The Second Circuit has distilled Rule 702’s requirements into three broad criteria: (1)

qualifications, (2) reliability, and (3) relevance and assistance to the trier of fact.” Jn re

LIBOR-Based Fin. Instruments Antitrust Litig., 299 F. Supp. 3d 430, 466 (S.D.N.Y.

2018) (citing Nimely v. City of New York, 414 F.3d 381, 396-97 (2d Cir. 2005)).

II. DISCUSSION

A, Dr. Dewitt’s Qualification to Offer Expert Testimony

Defendant first seeks to exclude testtmony from Dr. DeWitt on the ground that

she is not qualified to offer expert testimony. It bases this argument primarily on the

fact that while Dr. DeWitt offers opinions about DuPont’s failure to perform proper

human risk assessments, she has never performed one herself. Def.’s Mem. of Law at

pp. 8-12. This argument is unavailing.

An individual may be qualified to offer expert testimony “by knowledge, skill,

experience, training, or education.” FED. R. EVID. 702. In assessing whether an

individual is qualified to offer an expert opinion:

The totality of an expert’s qualifications should be considered in evaluating

whether or not his or her testimony is admissible. An expert need not be

precluded from testifying merely because he or she does not possess

experience tailored to the precise product or process that is the subject matter

of the dispute.

Hilaire v. DeWalt Indus. Tool Co., 54 F. Supp. 3d 223, 236 (E.D.N.Y. 2014) (internal

quotations and citations omitted). Under these standards, Dr. DeWitt clearly qualifies

as an expert witness. Her educational and professional background involve significant

study and work in the field of toxically or risk assessment. See generally DeWitt

Opinion at Ex. A. Her doctorate work included a concentration in risk assessment. She

has teaching and work experience in the conduct of risk assessments. The record amply

demonstrates that her background involves “knowledge, skill, experience, training, or

education” sufficient to render her qualified to offer an expert opinion in this case. FED.

R. Evib. 702. “Although she has not performed any studies herself, this does not mean

she is not qualified to give [an] opinion using her experience as well as a review of

relevant scientific literature.” In re Mirena IUD Prod. Liab. Litig., 169 F. Supp. 3d 396,

420 (S.D.N.Y. 2016).

B. Admissibility of the Second Opinion

The second opinion is that, based on information then available to it, DuPont was

required to conduct a human health risk assessment in the 1980s. DeWitt Opinion at p.

9. DuPont maintains that this opinion is based on nothing beyond Dr. DeWitt’s own

personal views and thus should be excluded because it lacks any scientific basis. Def.’s

Mem. of Law at pp. 15-17. It also argues that Dr. DeWitt improperly opines on the form

as to which such an assessment should have taken rendering her opinion unreliable. /d.

at pp. 17-21.

Plaintiffs oppose the Motion. They note first that DeWitt’s opinion is well

founded based on her review of toxicological and blood studies that were known to

DuPont in the 1970s and 1980s showing risk associated with PFOA. Pls.” Mem. of Law

at p. 10. They also note that evidence elsewhere in the record’ suggests that the

Environmental Protection Agency had outlined general protocols for risk assessments

in the 1980s and at least one official with DuPont used that protocol as a guide for

4) proposing an assessment program in the 1990s. /d. at pp. 11-12. In reviewing the

parties’ submissions on Defendant’s Motion for Summary Judgment, for example, it is

clear that the Environmental Protection Agency had, in the early 1980s, published

material on the need for risk assessment. Dkt. No. 418-10 at p. 17.4 The record certainly

demonstrates that there is a factual basis for Dr. DeWitt to testify about the nature of

risk assessments, what information was available about conducting such studies in the

1980s and 1990s, what information was available to DuPont that could or should have

led them to conduct such an assessment, and what form such an assessment should, in

her opinion have taken. As this Court has noted in the context of other recent Daubert

decisions in this case, a record certainly has been made from which a vigorous cross-

examination of the strength of these opinions can be tested. But that does not render the

DeWitt opinion completely inadmissible.

3 The Court notes that while Plaintiffs’ opposition to this Motion relies extensively on the deposition testimony of

Dr. Bogdanffy, Pls.’ Mem. of Law at p. 11, they have not included that transcript among the over dozen exhibits

offered in their responsive papers.

4 This page citation is to the page numbers provided by te Court’s CM/ECF system.

On one point, however, Defendant has carried its burden of warranting

preclusion. DeWitt’s Report opines that DuPont was “required” to conduct a risk

assessment in the 1980s based on information then known by DuPont and 3M. That

opinion does appear to lack a reliable basis in fact sufficient to permit its introduction to

“) the jury. It appears to the Court that the record is devoid of evidence that Dr. DeWitt

knew of any specific standard that mandated such a reporting requirement. She

specifically disclaimed such knowledge during her deposition:

Q. And so going back to my original question: In the 1980s, were there any

standards requiring DuPont to conduct a human health risk assessment

regarding potential adverse risks to human health from PFOA?

A. I don’t know the answer to that question. All I’m saying is that based on

what I had available to me at the time I wrote my report, J believe that they

should have conducted a thorough and comprehensive risk assessment.

Dkt. No. 402-3 at p. 67 (emphasis added). This answer goes even further when

disclaiming knowledge of “any standards.” Jd. DeWitt’s report also makes no

connection between any then-existing protocol that would have required DuPont to take

the actions set forth in her report. See generally DeWitt Report. This is especially true

given DeWitt’s separate testimony that she did not believe the EPA had standards

requiring chemical companies to conduct human health risk assessments. Dkt. No. 402-

3 at p. 66.

DuPont’s Motion to exclude what has been labeled the second opinion here,

therefore, is granted in part and denied in part as set forth above.

C. Admissibility of the Third Opinion

The Court reaches a different opinion regarding the third opinion, namely what

actions DuPont may have taken had a proper risk assessment been conducted. DeWitt

Opinion at p. 10. “[E]xpert testimony should be excluded if it is speculative or

conjectural.” Boucher v. U.S. Suzuki Motor Corp., 73 F.3d 18, 21 (2d Cir. 1996). Here,

nothing in the present record establishes a solid basis for Dr. DeWitt to opine on what

DuPont could have done decades ago if it had performed a particular type of study. She

does not even offer an opinion about what DuPont should have done, only that it could

have provided greater notice to customers or remove PFOA-related chemicals from

products altogether — her opinion simply is that DuPont could have done one or both of

“| these things. Defendant may have done exactly what DeWitt suggests, but it may not.

Dr. DeWitt does not appear to offer an opinion that DuPont was obligated to do either

by any legal authority nor by any industry standard. This opinion seems to be based

solely on a speculative assumption that had DuPont done a study it would have become

aware of information that could have led it to take the actions described. That is a multi-

level speculative assumption, the type of which Rule 702 does not permit. Car Freshner

Corp. v. Am. Covers, LLC, 2021 WL 4502281, at *9 (N.D.N.Y. Sept. 30, 2021) (citing

cases). On the present record, Dr. DeWitt’s opinion fails to pass the Daubert threshold

and should be precluded.

I. CONCLUSION

ACCORDINGLY, it is

ORDERED, that Defendant’s Motion (Dkt. No. 402) to exclude expert

testimony from Dr. Jamie DeWitt is GRANTED IN PART and DENIED IN PART

4) and it is further

ORDERED, that the Clerk of the Court shall serve copies of this Decision and

Order on the parties.

Dated: September 19, 2024

Albany, New York

Code “

U.SMMfagistrate Judge

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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