Marilyn Williams v. Boehringer Ingelheim Pharmaceuticals, Inc.

CourtCourt of Appeals for the Eleventh Circuit
DecidedNovember 7, 2022
Docket20-10306
StatusUnpublished

This text of Marilyn Williams v. Boehringer Ingelheim Pharmaceuticals, Inc. (Marilyn Williams v. Boehringer Ingelheim Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eleventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Marilyn Williams v. Boehringer Ingelheim Pharmaceuticals, Inc., (11th Cir. 2022).

Opinion

USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 1 of 18

[DO NOT PUBLISH] In the United States Court of Appeals For the Eleventh Circuit

____________________

No. 21-10305 ____________________

IN RE: ZANTAC (RANITIDINE) PRODUCTS LIABILITY LITIGATION ___________________________________________________ 9:20-cv-80555 ARTHUR CARTEE, Plaintiff-Appellant, versus BOEHRINGER INGELHEIM PHARMACEUTICALS, INC., PFIZER, INC., GLAXOSMITHKLINE LLC,

Defendants-Appellees. USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 2 of 18

2 Opinion of the Court 21-10305

No. 21-10306 ____________________

IN RE: ZANTAC (RANITIDINE) PRODUCTS LIABILITY LITIGATION __________________________________________________ 9:20-cv-80512-RLR MARILYN WILLIAMS, Plaintiff-Appellant, versus BOEHRINGER INGELHEIM PHARMACEUTICALS, INC., BOEHRINGER INGELHEIM USA CORPORATION, WALGREENS BOOT ALLIANCE, INC.,

Defendants-Appellees.

Appeals from the United States District Court for the Southern District of Florida D.C. Docket No. 9:20-md-02924-RLR ____________________ USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 3 of 18

21-10305 Opinion of the Court 3

Before JORDAN and LAGOA, Circuit Judges.* PER CURIAM: The appellants, Arthur Cartee and Marilyn Williams, are two of the thousands of plaintiffs alleging personal injury claims in In re Zantac (Ranitidine), MDL No. 2924. Because there is no final district court decision with respect to the amended complaints of Mr. Cartee and Ms. Williams, we dismiss their appeals for lack of appellate jurisdiction. I Mr. Cartee and Ms. Williams both alleged that they took ranitidine products to treat mild heartburn. Starting in 2006, Mr. Cartee began taking both prescription and over-the-counter ge- neric ranitidine. He developed prostate cancer in 2012. Ms. Wil- liams started taking Zantac, an over-the-counter brand-name drug, in 2011. She was diagnosed with abdominal and ovarian cancer in 2016. A On February 6, 2020, the U.S. Judicial Panel on Multidistrict Litigation created an MDL in the Southern District of Florida— MDL No. 2924—for purposes of centralizing pretrial proceedings in actions alleging that ranitidine, the active ingredient in Zantac,

* After oral argument, Judge Luck recused himself from this case. This opinion is therefore issued by a quorum. See 28 U.S.C. § 46(d); 11th Cir. R. 34-2. USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 4 of 18

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breaks down to form an alleged carcinogen known as N-Nitrosodi- methylamine (NDMA). After the MDL was created, Mr. Cartee and Ms. Williams each filed separate federal lawsuits—Mr. Cartee in Illinois and Ms. Williams in Alabama—alleging that ranitidine caused their cancers. Their actions were transferred to the MDL. A few months after the transfers, the parties filed a proposed order coordinating the filings of master complaints. This order, known as Pretrial Order # 31, was adopted and entered by the dis- trict court. The Order required the personal injury plaintiffs to “file a Master Personal Injury Complaint [or MPIC] on behalf of all Plain- tiffs asserting personal injury claims in MDL No. 2924.” MDL D.E. 876 at 2. The Order stated that “[a]ll claims pleaded in the [MPIC] will supersede and replace all claims pleaded in any complaint pre- viously filed in or transferred to MDL No. 2924 . . . .” Id. In addition, the Order directed the personal injury plaintiffs to attach a Master Short Form Complaint (or SFC) to serve as a template “for each individual case.” Id. The individual plaintiffs were to provide certain information, such as their names, injuries, places of residence, and the defendants being sued. See id. The SFCs took the form of a worksheet that allowed each plaintiff to fill in the blanks as to who was being sued and to check boxes for which claims were being asserted. See id. The SFC also contained a clause indicating that it incorporated all allegations from the USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 5 of 18

21-10305 Opinion of the Court 5

MPIC. See id. The Order stated that, “[f]or each action directly filed in or transferred to MDL No. 2924 subject to this Order, the [MPIC] together with the Short Form Complaint shall be deemed the operative Complaint.” Id. at 3. 1 Shortly thereafter, the personal injury plaintiffs filed the MPIC. The MPIC named no individual plaintiffs. Instead, it incor- porated them by reference. The MPIC states it “is not intended to consolidate for any purpose the separate claims of the individual Plaintiffs in this MDL,” and that it “does not constitute waiver or dismissal of any actions or claims asserted in those individual ac- tions.” MDL D.E. 887 at 2. The MPIC refers to the plaintiffs’ cases as individual “actions” throughout. See id. at ¶¶ 216, 434–35. As directed, Mr. Cartee and Ms. Williams both filed short form complaints to go with the MPIC. In his SFC, Mr. Cartee sued four brand-name manufacturers (Boehringer, GlaxoSmithKline, Sanofi, and Sanofi-Aventis) and

1 MDL No. 2924 therefore “employe[d] the device of a master complaint, sup- plemented by individual short-form complaints that adopt the master com- plaint in whole or in part.” In re Zofran (Ondansetron) Products Liability Litig., MDL No. 1:15-md-2657-FDS, 2017 WL 1458193, at *6 (D. Mass. Apr. 24, 2017). The master complaint contained allegations common to all plaintiffs asserting the same types of claims, while the short-form complaints contained allegations specific to each individual plaintiff. See In re Taxotere (Docetexel) Prod. Liab. Litig., 995 F.3d 384, 387 (5th Cir. 2021). See also Manual for Com- plex Litigation (Fourth) § 40.52 (Fed. Jud. Ctr. 2004) (providing sample case management order governing mass tort claims using master and short-form complaints). USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 6 of 18

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two retailers (Walgreens and Walmart). He checked the boxes for Counts I–XIII of the MPIC, leaving out only Count XIV (a survival action) and Count XV (a wrongful death claim). As discussed be- low, he filed an amended SFC shortly thereafter, dropping the Sanofi entities from the list of brand-name defendants from which he sought to recover. In her SFC, Ms. Williams sued two brand name manufactur- ers (Boehringer Ingelheim Pharmaceuticals and Boehringer Ingel- heim USA) and one retailer (Walgreens), and she indicated that any distributors and repackagers she might sue were then unknown. She checked the boxes for five different counts in the MPIC, includ- ing those asserting claims for strict products liability, failure to warn, and breaches of warranties. Like Mr. Cartee, and as dis- cussed below, Ms. Williams later amended her SFC. B The district court dismissed the entire MPIC without preju- dice as a shotgun pleading. See MDL D.E. 2515 at 13. In a separate order, the court also held that any claims “based on an allegation that a brand-name drug’s FDA-approved formulation renders the drug misbranded” were preempted by the Food, Drug, and Cos- metics Act, 21 U.S.C. § 301 et. seq., “because the drug’s manufac- turer cannot independently and lawfully change a drug formula- tion that the FDA has approved.” MDL D.E. 2532 at 24. The court ordered the personal injury plaintiffs to omit misbranding allega- tions if they amended the MPIC. Id. at 25. USCA11 Case: 21-10306 Date Filed: 11/07/2022 Page: 7 of 18

21-10305 Opinion of the Court 7

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