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Case TitleNew York Times Company et al v. U.S. Food and Drug Administration
DistrictSouthern District of New York
CityFoley Square
Case Number1:2019cv04740
Date Filed2019-05-22
Date Closed2021-06-21
JudgeJudge Valerie E. Caproni
PlaintiffNew York Times Company
PlaintiffSheila Kaplan
Case DescriptionNew York Times reporter Sheila Kaplan submitted two FOIA requests to the FDA for records concerning Juul Labs. The agency acknowledged receipt of the requests. The agency told Kaplan that her first request would require pre-disclosure notification to obtain the company's confidentiality claims. In response to Kaplan's second FOIA request, the agency withheld the records under Exemption 7(A) (interference with ongoing investigation or proceeding). Kaplan filed an administrative appeal of the agency's decision. After hearing nothing further from the agency pertaining to either request, Kaplan and the New York Times Company filed suit.
Complaint issues: Failure to respond within statutory time limit, Adequacy - Search, Litigation - Attorney's fees

DefendantU.S. Food and Drug Administration
Documents
Docket
Complaint
Opinion/Order [15]
Opinion/Order [38]
FOIA Project Annotation: A recent decision from the Southern District of New York serves as a reminder of how unsettled some aspects of Exemption 4 (commercial and confidential) remain in the aftermath of the 2019 Supreme Court decision in Food Marketing Institute v. Argus Leader Media, 139 S. Ct. 2356 (2019), in which the Court abandoned the substantial harm test that first appeared in the D.C. Circuit's 1974 National Parks decision because it was not supported by the plain language of Exemption 4, concluding instead that records were protected under Exemption 4 when they contained commercial information that had been submitted with an expectation of confidentiality. However, since the government had assured confidentiality for the data at issue in Argus Media if the Supreme Court ruled in favor of the trade association, the Court did not go into detail about what needed to be shown to establish confidentiality, indicating instead that it was more than just asserting that information was confidential but less than an explicit assurance of confidentiality from the agency. The case involved two requests from New York Times reporter Sheila Kaplan for records concerning Juul Labs, particularly the use of its products by minors. Kaplan submitted her requests after the FDA sent a letter to Juul requesting records under Section 904(b) of the Food, Drug and Cosmetic Act related to Juul's marketing practices, research on marketing, public health impact, and adverse experiences and complaints, Kaplan submitted a FOIA request to the agency for records obtained from Juul in response to the FDA's request. She submitted a second request for records concerning marketing, advertising, and sales strategy records obtained by the FDA from Juul during its inspection of the company's headquarters in September 2018. The agency told Kaplan that it had sent a pre-disclosure notification letter to Juul pertaining to records responsive to her first request but that because its inspection had not yet been completed, it was withholding records responsive her second request under Exemption 7(A) (interference with ongoing investigation or proceeding). Based on an Index of Document Categories provided by Juul to the FDA in response to its pre-disclosure notification letter, Kaplan told the agency the Times would contest the Exemption 4 claims for a category entitled Consumer Experience. District Court Judge Valerie Caproni found the FDA had "failed to demonstrate the commercial nature of these records. Neither customer nor non-customer complaints are properly classified as commercial information under Exemption 4, at least as described in this case. Juul's internal classification and analysis of these complaints may, however, be appropriately described as commercial and therefore entitled to protection under Exemption 4. Because the FDA has failed to provide sufficient details on the nature of any internal Juul communications or analysis, the Court cannot make a reasoned determination that this information qualifies as commercial. FDA has also failed entirely to address whether Juul's internal analysis can be segregated from the complaints themselves." The FDA argued that the complaints were protected under Public Citizen v. Dept of Health and Human Services, 66 F. Supp. 3d 196 (D.D.C. 2014), in which the court found that disclosure log summaries submitted by pharmaceutical companies in annual reports were commercial. But Caproni observed that "this Court does not read Public Citizen to stand for the extremely broad proposition suggested by the FDA that any interaction between a company and its customers is necessarily commercial information." Instead, she noted that "it is not the bare interaction between a company and its customer that makes the interaction commercial; the interaction is commercial because of what it reveals about the company's internal or income-producing activities." She indicated that "the same cannot be said for one-sided interactions to the company. Such a complaint, without more, does not threaten to reveal anything about a company's internal operations and is meaningfully different than a sales meeting between a salesperson and a customer." She also faulted the FDA's description of records characterized as internal Juul analysis and communications. She indicated that the agency's current Vaughn index was insufficient to carry its burden of proof on the issue of whether these records were commercial. She pointed out that "although these records may contain information appropriately classified as commercial under Exemption 4, because neither FDA's amended Vaughn index nor the [agency's] declaration provides an adequate foundation for Court review, summary judgment for the FDA is inappropriate at this time." Noting that the Supreme Court's decision in Argus Media had left unsettled the required assurances of confidentiality the agency and the business submitter needed to show, Caproni rejected the FDA's claim that Argus Media "instructs courts to focus on how the person who provides the documents to the Government treats them. Here, the FDA argues, Juul is the 'person' that provided the records to FDA, and Juul itself treats these records as confidential. That, FDA argues, ends the inquiry." Instead, Caproni noted that "it strains credulity to believe that Juul treats customer and non-customer complaints and Juul's responses as highly confidential information." She explained that "where third-party disclosure has been deemed consistent with the finding that a company treated the information as confidential, there has been some accompanying indication that the company took steps to ensure that the information remained closely held or guarded, or there was at least an implicit understanding that the information would remain limited to a select audience." She observed that "without any indication from FDA or Juul that complainants submitted their complaints to Juul with an understanding that the complaints were to be kept confidential, the Court finds no reason to stamp them with a label of 'confidential information.'" Caproni, however, agreed the agency had provided an explicit assurance of confidentiality to Juul in its letter requesting records under Section 904(b). The Times argued that the agency's assurances of privacy were nothing more than a recitation of the standard under Exemption 4 and that to satisfy the confidentiality prong of Argus Leader, the government needed to provide "a particularized promise of confidentiality, specific to the documents provided." The Times also contended that under the broad standard enunciated by the FDA, a company could claim confidentiality for any document submitted. Caproni noted that "but Plaintiffs ignore a third option, in which an agency's records collection is accompanied by an express notice of its intention to make public the collected records. In that scenario a company cannot reasonably claim to have received an assurance of privacy, because there would be no expectation that any information submitted, regardless of whether it otherwise meets the hallmarks of confidential commercial information under Exemption 4, would be kept private by the agency."
Issues: Exemption 4 - Confidential business information
User-contributed Documents
 
Docket Events (Hide)
Date FiledDoc #Docket Text

2019-05-221COMPLAINT against U.S. Food and Drug Administration. (Filing Fee $ 400.00, Receipt Number ANYSDC-16937957)Document filed by Sheila Kaplan, New York Times Company.(McCraw, David) (Entered: 05/22/2019)
2019-05-222FILING ERROR - CORPORATE PARENT/OTHER AFFILIATE NOT ADDED - RULE 7.1 CORPORATE DISCLOSURE STATEMENT. No Corporate Parent. Document filed by New York Times Company.(McCraw, David) Modified on 5/23/2019 (ldi). (Entered: 05/22/2019)
2019-05-223REQUEST FOR ISSUANCE OF SUMMONS as to U.S. Food and Drug Administration, re: 1 Complaint. Document filed by Sheila Kaplan, New York Times Company. (McCraw, David) (Entered: 05/22/2019)
2019-05-224CIVIL COVER SHEET filed. (McCraw, David) (Entered: 05/22/2019)
2019-05-23CASE OPENING INITIAL ASSIGNMENT NOTICE: The above-entitled action is assigned to Judge Valerie E. Caproni. Please download and review the Individual Practices of the assigned District Judge, located at http://nysd.uscourts.gov/judges/District . Attorneys are responsible for providing courtesy copies to judges where their Individual Practices require such. Please download and review the ECF Rules and Instructions, located at http://nysd.uscourts.gov/ecf_filing.php . (dnh) (Entered: 05/23/2019)
2019-05-23Magistrate Judge Henry B. Pitman is so designated. Pursuant to 28 U.S.C. Section 636(c) and Fed. R. Civ. P. 73(b)(1) parties are notified that they may consent to proceed before a United States Magistrate Judge. Parties who wish to consent may access the necessary form at the following link: http://nysd.uscourts.gov/forms.php . (dnh) (Entered: 05/23/2019)
2019-05-23Case Designated ECF. (dnh) (Entered: 05/23/2019)
2019-05-235ELECTRONIC SUMMONS ISSUED as to U.S. Food and Drug Administration. (dnh) (Entered: 05/23/2019)
2019-05-23***NOTICE TO ATTORNEY TO RE-FILE DOCUMENT - DEFICIENT DOCKET ENTRY ERROR. Notice to Attorney David Edward McCraw to RE-FILE Document 2 Rule 7.1 Corporate Disclosure Statement. ERROR(S): Corporate Parents/Other affiliates were not added. Please re-file this document and when prompted: Are there any corporate parents or other affiliates?, select the YES radio button and enter the Corporate Parent(s) or Affiliate(s). (ldi) (Entered: 05/23/2019)
2019-05-236NOTICE OF APPEARANCE by Dana Robinson Green on behalf of Sheila Kaplan, New York Times Company. (Green, Dana) (Entered: 05/23/2019)
2019-05-237RULE 7.1 CORPORATE DISCLOSURE STATEMENT. Identifying Other Affiliate BlackRock, Inc. for New York Times Company, Sheila Kaplan. Document filed by Sheila Kaplan, New York Times Company.(McCraw, David) (Entered: 05/23/2019)
2019-05-248NOTICE OF INITIAL PRETRIAL CONFERENCE: Initial Conference set for 7/19/2019 at 10:00 AM in Courtroom 443, 40 Centre Street, New York, NY 10007 before Judge Valerie E. Caproni, as further set forth in this order. (Signed by Judge Valerie E. Caproni on 5/24/2019) (jwh) (Entered: 05/24/2019)
2019-06-279NOTICE OF APPEARANCE by Charles Salim Jacob on behalf of U.S. Food and Drug Administration. (Jacob, Charles) (Entered: 06/27/2019)
2019-06-2710ANSWER to 1 Complaint. Document filed by U.S. Food and Drug Administration.(Jacob, Charles) (Entered: 06/27/2019)
2019-07-1111JOINT LETTER MOTION to Adjourn Conference and Joint Submission in Advance of the Initial Pretrial Conference with a Proposed Schedule addressed to Judge Valerie E. Caproni from Charles S. Jacob dated July 11, 2019. Document filed by U.S. Food and Drug Administration.(Jacob, Charles) (Entered: 07/11/2019)
2019-07-1112ORDER: granting 11 Letter Motion to Adjourn Conference. Application GRANTED. The parties' proposed productions schedule is ADOPTED. The IPTC is ADJOURNED to November 22, 2019, at 10:00 a.m. In their November 15, 2019 status update, inaddition to proposing a schedule for briefing any motions for summary judgment, the parties must inform the Court whether, in their view, the IPTC would be beneficial or should be cancelled. SO ORDERED. Initial Conference set for 11/22/2019 at 10:00 AM before Judge Valerie E. Caproni. (Signed by Judge Valerie E. Caproni on 7/11/2019) (ama) (Entered: 07/11/2019)
2019-11-08Magistrate Judge Sarah L. Cave is so redesignated. (wb) (Entered: 11/08/2019)
2019-11-08NOTICE OF REDESIGNATION TO ANOTHER MAGISTRATE JUDGE. The above entitled action has been redesignated to Magistrate Judge Sarah L Cave. Please note that this is a reassignment of the designation only. (wb) (Entered: 11/08/2019)
2019-11-0813NOTICE OF APPEARANCE by Alexandra Perloff-Giles on behalf of Sheila Kaplan, New York Times Company. (Perloff-Giles, Alexandra) (Entered: 11/08/2019)
2019-11-1514JOINT LETTER MOTION to Adjourn Conference and Joint Status Report addressed to Judge Valerie E. Caproni from Charles S. Jacob dated November 15, 2019. Document filed by U.S. Food and Drug Administration.(Jacob, Charles) (Entered: 11/15/2019)
2019-11-2015ORDER: granting in part 14 Letter Motion to Adjourn Conference. Application GRANTED in part. The Court adopts the parties' proposed schedule as modified. If Juul moves to intervene in this case, the Court will at that time determine whether the motion is timely. But the Court warns Juul that is unlikely to significantly modify the proposed schedule, thus Juul should make a timely decision whether to move to intervene. The conference scheduled for November 22, 2019, is CANCELLED. SO ORDERED. (Signed by Judge Valerie E. Caproni on 11/20/2019) (ama) (Entered: 11/20/2019)
2020-01-0316JOINT LETTER addressed to Judge Valerie E. Caproni from Alexandra Perloff-Giles dated January 3, 2020 re: The New York Times Company et al. v. Food and Drug Administration (19-cv-4740). Document filed by Sheila Kaplan, New York Times Company.(Perloff-Giles, Alexandra) (Entered: 01/03/2020)
2020-02-1117CONSENT LETTER MOTION for Extension of Time to File Summary Judgment Papers addressed to Judge Valerie E. Caproni from Charles S. Jacob dated February 11, 2020. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 02/11/2020)
2020-02-1218ORDER granting 17 Letter Motion for Extension of Time. Application Granted. So ordered. Motions due by 3/3/2020. (Signed by Judge Valerie E. Caproni on 2/12/2020) (js) (Entered: 02/13/2020)
2020-02-12Set/Reset Deadlines: Cross Motions due by 3/31/2020. Responses due by 4/14/2020 Replies due by 4/28/2020. (js) (Entered: 02/13/2020)
2020-03-0319MOTION for Summary Judgment . Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 03/03/2020)
2020-03-0320MEMORANDUM OF LAW in Support re: 19 MOTION for Summary Judgment . . Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 03/03/2020)
2020-03-0321DECLARATION of Sarah B. Kotler in Support re: 19 MOTION for Summary Judgment .. Document filed by U.S. Food and Drug Administration. (Attachments: # 1 Exhibit A - FOIA Request 2018-5116, # 2 Exhibit B - Section 904(b) Letter, # 3 Exhibit C - FOIA Request 2018-8462, # 4 Exhibit D - Exemption 7A Denial Letter).(Jacob, Charles) (Entered: 03/03/2020)
2020-03-0322DECLARATION of Marqui Q. Barnes in Support re: 19 MOTION for Summary Judgment .. Document filed by U.S. Food and Drug Administration. (Attachments: # 1 Exhibit A - November 9, 2018, Predisclosure Notice, # 2 Exhibit B - July 16, 2019, Predisclosure Notice, # 3 Exhibit C - Vaughn Index).(Jacob, Charles) (Entered: 03/03/2020)
2020-03-0323DECLARATION of Joanna Engelke in Support re: 19 MOTION for Summary Judgment .. Document filed by U.S. Food and Drug Administration. (Attachments: # 1 Exhibit A - 904(b) Request).(Jacob, Charles) (Entered: 03/03/2020)
2020-03-2424JOINT LETTER addressed to Judge Valerie E. Caproni from Alexandra Perloff-Giles dated March 24, 2020 re: The New York Times Company et al. v. Food and Drug Administration (19-cv-4740). Document filed by Sheila Kaplan, New York Times Company..(Perloff-Giles, Alexandra) (Entered: 03/24/2020)
2020-03-3125CROSS MOTION for Summary Judgment . Document filed by Sheila Kaplan, New York Times Company. Responses due by 4/14/2020.(McCraw, David) (Entered: 03/31/2020)
2020-03-3126MEMORANDUM OF LAW in Support re: 25 CROSS MOTION for Summary Judgment . . Document filed by Sheila Kaplan, New York Times Company..(McCraw, David) (Entered: 03/31/2020)
2020-03-3127DECLARATION of David E. McCraw in Support re: 25 CROSS MOTION for Summary Judgment .. Document filed by Sheila Kaplan, New York Times Company..(McCraw, David) (Entered: 03/31/2020)
2020-04-1028CONSENT LETTER MOTION for Extension of Time to File FDA's Combined Response to Plaintiffs Cross-motion For Summary Judgment and Reply in Support of its Motion for Summary Judgment addressed to Judge Valerie E. Caproni from Charles S. Jacob dated April 10, 2020. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 04/10/2020)
2020-04-1329ORDER granting 28 Letter Motion for Extension of Time. Application Granted. So Ordered. (Signed by Judge Valerie E. Caproni on 4/13/2020) (js) (Entered: 04/13/2020)
2020-04-13Set/Reset Deadlines: Responses due by 5/5/2020 Replies due by 5/26/2020. (js) (Entered: 04/13/2020)
2020-05-0130CONSENT LETTER MOTION for Extension of Time to File Response/Reply addressed to Judge Valerie E. Caproni from Charles S. Jacob dated May 1, 2020. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 05/01/2020)
2020-05-0431ORDER: granting 30 Letter Motion for Extension of Time to File Response/Reply re 30 CONSENT LETTER MOTION for Extension of Time to File Response/Reply addressed to Judge Valerie E. Caproni from Charles S. Jacob dated May 1, 2020. Application Granted. SO ORDERED. Replies due by 6/26/2020. (Signed by Judge Valerie E. Caproni on 5/01/2020) (ama) (Entered: 05/04/2020)
2020-06-0532MEMORANDUM OF LAW in Opposition re: 25 CROSS MOTION for Summary Judgment . and in Further Support of FDA's Motion for Summary Judgment . Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 06/05/2020)
2020-06-0533DECLARATION of Marqui Q. Barnes in Support re: 19 MOTION for Summary Judgment .. Document filed by U.S. Food and Drug Administration. (Attachments: # 1 Exhibit A - Amended Vaughn Index).(Jacob, Charles) (Entered: 06/05/2020)
2020-06-2634REPLY MEMORANDUM OF LAW in Support re: 25 CROSS MOTION for Summary Judgment . . Document filed by Sheila Kaplan, New York Times Company..(McCraw, David) (Entered: 06/26/2020)
2020-06-2635DECLARATION of Alexandra Perloff-Giles in Support re: 25 CROSS MOTION for Summary Judgment .. Document filed by Sheila Kaplan, New York Times Company..(McCraw, David) (Entered: 06/26/2020)
2021-01-2136LETTER addressed to Judge Valerie E. Caproni from Charles S. Jacob dated January 21, 2021 re: Recent Supplemental Authority. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 01/21/2021)
2021-01-2237MEMO ENDORSEMENT on re: 36 Letter filed by U.S. Food and Drug Administration. ENDORSEMENT: Plaintiffs may respond to Defendant's letter not later than January 29, 2021. (Signed by Judge Valerie E. Caproni on 1/22/2021) (cf) (Entered: 01/22/2021)
2021-03-2938OPINION AND ORDER re: 19 MOTION for Summary Judgment filed by U.S. Food and Drug Administration, 25 CROSS MOTION for Summary Judgment filed by New York Times Company, Sheila Kaplan. For the foregoing reasons, FDA's motion for summary judgment is DENIED without prejudice and Plaintiffs' cross-motion for summary judgment is DENIED without prejudice. FDA is instructed to submit a revised Vaughn index addressing internal Juul classifications, analyses, or communications concerning consumer and non-consumer complaints. FDA must also supplement the Vaughn index entries concerning the records in the Consumer Research and Strategy category. Finally, FDA must submit a segregability analysis concerning any records that contain internal Juul analysis or communication in addition to complaints and Juul's responses to complaints. To the extent FDA seeks to continue withholding the contested records, it must submit a renewed motion for summary judgment along with the above materials not later than May 17, 2021. Plaintiffs may submit a renewed cross-motion for summary judgment not later than June 14, 2021. The Court also encourages the parties to meet-and-confer in light of this opinion to determine whether further motion practice can be obviated by a mutually agreeable production of records. The Clerk of Court is respectfully requested to terminate the open motions at Dkt. 19 and Dkt. 25. ( Cross Motions due by 6/14/2021., Motions due by 5/17/2021.) (Signed by Judge Valerie E. Caproni on 3/29/2021) (mro) (Entered: 03/29/2021)
2021-05-0639INTERNET CITATION NOTE: Material from decision with Internet citation re: 38 Memorandum & Opinion, Set Deadlines. (sjo) (Entered: 05/06/2021)
2021-05-1340JOINT LETTER MOTION for Extension of Time and Status Update addressed to Judge Valerie E. Caproni from Charles S. Jacob dated May 13, 2021. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 05/13/2021)
2021-05-1341ORDER granting 40 Letter Motion for Extension of Time. Application GRANTED. The parties' deadlines to file summary judgment motions and accompanying documents are ADJOURNED sine die. Not later than June 15, 2021, the parties must file a joint letter on the status of FDA's productions and the parties' efforts to resolve this matter without additional motion practice. To the extent the parties are unable to reach a mutually agreeable resolution on all issues, the parties must include a proposed briefing schedule on any renewed motions for summary judgment in their June 15, 2021 letter. So Ordered. (Signed by Judge Valerie E. Caproni on 5/13/2021) (js) (Entered: 05/14/2021)
2021-06-1542JOINT LETTER addressed to Judge Valerie E. Caproni from Charles S. Jacob dated June 15, 2021 re: Joint Status Letter. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 06/15/2021)
2021-06-1643MEMO ENDORSEMENT on re: 42 Letter filed by U.S. Food and Drug Administration. ENDORSEMENT: Application GRANTED. Not later than June 21, 2021, the parties must submit a stipulation and proposed order dismissing Plaintiffs' remaining claims in this action. Not later than August 31, 2021, to the extent the parties have been unable to resolve privately any fee- related issues, Plaintiffs must submit any applications for attorneys' fees. So Ordered.(Motions due by 8/31/2021.) (Signed by Judge Valerie E. Caproni on 6/16/2021) (js) (Entered: 06/16/2021)
2021-06-2144PROPOSED STIPULATION AND ORDER. Document filed by U.S. Food and Drug Administration..(Jacob, Charles) (Entered: 06/21/2021)
2021-06-2145STIPULATION AND ORDER OF DISMISSAL: WHEREAS, IT IS HEREBY STIPULATED, AGREED, and ORDERED as follows: The productions set forth above fully resolve any and all claims that Plaintiffs now have or may hereinafter acquire against FDA or the United States of America (the "United States"), or any department, agency, officer, or employee of Defendant and/or the United States, related to or arising out of the FOIA Requests, except for any claims for attorneys' fees and costs by Plaintiffs under 5 U.S.C. § 552(a)(4)(E). Plaintiffs reserve the right to file a claim for fees and costs pursuant to 5 U.S.C. § 552(a)(4)(E), and Defendant reserves its right to oppose any such application. Pursuant to Rule 41(a)(2) of the Federal Rules of Civil Procedure, this action is hereby dismissed with prejudice; provided, however, that the Court shall retain jurisdiction to adjudicate a request by Plaintiffs for attorneys' fees and costs under 5 U.S.C. § 552(a)(4)(E). The Clerk of Court is respectfully directed to terminate all open motions and to close this case. SO ORDERED. (Signed by Judge Valerie E. Caproni on 6/21/2021) (ama) (Entered: 06/21/2021)
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