Opinion

Desch v. Merz North America, Inc.

Court
District Court, E.D. New York
Filed
Jul 28, 2022
Cited by
0 cases
Authority
More cited than 26.7%

explaining that “compelling” reasons are required to seal documents filed “in connection with dispositive motions such as motions for dismissal or summary judgment”

How later courts described this case

  • explaining that “compelling” reasons are required to seal documents filed “in connection with dispositive motions such as motions for dismissal or summary judgment”

Written by the judges who cited it.

The opinion

UNITED STATES DISTRICT COURT

EASTERN DISTRICT OF NEW YORK

INNA DESCH,

MEMORANDUM & ORDER

Plaintiff, 22-CV-02688 (HG)

v.

ULTHERA, INC. and MERZ NORTH

AMERICA, INC.,

Defendants.

Plaintiff has asserted various products liability and other common law claims related to

her use of Defendants’ medical device that the parties have referred to alternatively as the

“Ulthera system” and the “Ultherapy [s]ystem.” See ECF No. 17 at ¶¶ 3–7, 131–232; ECF No.

18-1 at 1. Defendants have filed a motion to dismiss Plaintiff’s Amended Complaint in its

entirety, see ECF No. 18, and included a placeholder document as one of the exhibits in support

of their motion, see ECF No. 18-4. The placeholder document corresponds to a petition that

Defendants submitted to the U.S. Food and Drug Administration (“FDA”) in 2007 seeking

permission to market the Ulthera system. See ECF No. 18-3 ¶ 5. Defendants filed concurrently

with their motion to dismiss a motion seeking permission to file under seal an excerpted version

of that FDA petition, and Defendants’ motion to seal included a proposed copy of those excerpts

for the Court’s consideration. See ECF Nos. 19, 19-2. For the reasons described below, the

Court finds that Defendants’ proposed exhibit is unnecessary to decide Defendants’ motion to

dismiss and therefore denies Defendants’ motion to seal and instead strikes Defendants’

proposed exhibit from the docket. The Court will not rely on the excerpts of Defendants’ FDA

petition in any future decision on Defendants’ motion to dismiss Plaintiff’s Amended Complaint.

To determine whether Defendants may file under seal excerpts of their FDA petition, the

Court must first determine whether the petition is a “judicial document[]” “subject to a

presumptive right of public access, whether on common law or First Amendment grounds.”

United States v. HSBC Bank USA, N.A., 863 F.3d 125, 134 (2d Cir. 2017). If the petition is a

judicial document, then the Court “must determine the weight of that presumption” of access and

“balance competing considerations against it” such as “the privacy interests of those resisting

disclosure.” Lugosch v. Pyramid Co. of Onondaga, 435 F.3d 110, 119–20 (2d Cir. 2006)

(internal quotation marks and citations omitted).

Defendants seek to file excerpts of their FDA petition to support their motion to dismiss

Plaintiff’s Amended Complaint in its entirety. “Court filings in connection with a motion to

dismiss are . . . judicial documents, and are generally entitled to a strong presumption of public

access.” Alcon Vision, LLC v. Lens.com, No. 18-cv-0407, 2020 WL 3791865, at *6 (E.D.N.Y.

July 7, 2020) (internal quotation marks and citations omitted); see also Brown v. Maxwell, 929

F.3d 41, 50 (2d Cir. 2019) (explaining that “compelling” reasons are required to seal documents

filed “in connection with dispositive motions such as motions for dismissal or summary

judgment”). A document that contains trade secrets or other “highly competitive business

information” may typically be filed under seal at least in part. P&L Dev., LLC v. Gerber Prods.

Co., No. 21-cv-5382, 2022 WL 1441999, at *3 (E.D.N.Y. May 6, 2022). Defendants assert that

their FDA petition satisfies this criteria because, at the time the petition was submitted to the

FDA, it was designated as exempt from the FDA’s disclosure obligations under the Freedom of

Information Act. See ECF No. 19 at 2 (citing 21 § C.F.R. 20.61). However, “judicial precedent

does not afford blanket protection against disclosure of communications with the FDA” even if

those communications have been designated as confidential and not been made public. King

Pharms., Inc. v. Eon Labs, Inc., No. 04-cv-5540, 2010 WL 3924689, at *8 (E.D.N.Y. Sept. 28,

2010).

Defendants’ motion to dismiss cites their FDA petition to support their argument that

FDA regulations—and the FDA’s corresponding approval of the Ulthera system pursuant to

those regulations—preempt Plaintiff’s common law claims arising under state law. See ECF No.

18-1 at 6–10. Specifically, Defendants cite the FDA petition as support for their assertion that

Defendants’ request for FDA approval of the Ulthera system included “bench testing, testing on

animal and cadaver tissue, human clinical trials, and proposed labeling and instructions.” See id.

at 2; see also id. at 9 (explaining that the petition “included clinical trials in humans as well as

draft instructions for use”). However, this same information is independently apparent from two

documents that Defendants have publicly filed in support of their motion to dismiss: (i) the

FDA’s letter granting Defendant Ulthera, Inc. permission to market the Ulthera system, subject

to the requirements of a particular FDA guidance document; and (ii) the FDA’s public guidance

document that specifies requirements for animal testing, clinical testing, and labeling. See ECF

No. 18-5 at 3–4; ECF No. 18-6 at 8–12. Accordingly, the additional level of detail included in

Defendants’ proposed excerpt of their FDA petition is “unnecessary at this stage of the

litigation,” and “the exhibit[] should be stricken from the docket” rather than filed under seal.

Blatt v. City of New York, No. 19-cv-1227, 2019 WL 1367605, at *3 (S.D.N.Y. Mar. 26, 2019);

see also Brown, 929 F.3d at 51–52 (explaining that a court may use its “supervisory power over

its own records and files” to strike from the docket records that are “redundant, immaterial, [or]

impertinent” even if those records do not meet the criteria to file under seal).

For the reasons explained above, the Court denies Defendants’ motion to file under seal

an excerpted version of their FDA petition as an exhibit in support of their motion to dismiss

Plaintiff’s Amended Complaint. The information contained in Defendants’ proposed excerpt of

the FDA petition is not relevant to the Court’s eventual decision on Defendants’ motion to

dismiss. The Court has therefore struck from the docket ECF No. 19-2, which contained

Defendants’ proposed excerpts of the petition. The Court’s decision on this motion is without

prejudice to Defendants seeking to file under seal part or all of their FDA petition at a later stage

of this litigation if and when the information in the petition becomes relevant.

SO ORDERED.

/s/ Hector Gonzalez .

HECTOR GONZALEZ

United States District Judge

Dated: Brooklyn, New York

July 28, 2022

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.

A word about cookies

We need a few to keep you signed in and the library working. The rest help us see which pages people use and where they get stuck. They stay off unless you say yes.