Opinion

Waters v. Celebrity Cruises, Inc.

Court
District Court, S.D. Florida
Filed
Jan 26, 2024
Cited by
0 cases
Authority
More cited than 20.2%

The opinion

UNITED STATES DISTRICT COURT

SOUTHERN DISTRICT OF FLORIDA

Case No. 22-cv-22913-BLOOM/Torres

MARIETTE WATERS,

Plaintiff,

v.

CELEBRITY CRUISES, INC.

a Foreign Corporation.

Defendant.

__________________________________/

ORDER ON MOTION FOR LEAVE TO FILE MOTION IN LIMINE

THIS CAUSE is before the Court upon Defendant Celebrity Cruises, Inc.’s (“Defendant”)

Motion for Leave to File its Motion in Limine (“Motion”), ECF No. [82]. Plaintiff Mariette Waters

(“Plaintiff”) filed a Response, (“Response”), ECF No. [84], to which Defendant filed a Reply

(“Reply”), ECF No. [90]. The Court has reviewed the Motion, all supporting and opposing

submissions, the record in this case, the applicable law, and is otherwise fully advised. For the

reasons set forth below, Defendant’s Motion is denied.

I. BACKGROUND

This medical negligence action stems from a blood transfusion Plaintiff received aboard

Defendant’s vessel whereby Plaintiff alleges she contracted the human immunodeficiency virus

(HIV). See ECF No. [1] ¶ 4.

On December 4, 2023, Defendant moved to file a late Motion seeking to preclude reference

to the U.S. Food and Drug Administration (“FDA”) Regulations or its Processes. ECF No. [82]

at 1. The deadline to file all pre-trial motions, including motions in limine, was November 8, 2023,

as set forth in this Court’s Amended Scheduling Order. ECF No. [37] at 2. Both parties filed

motions on the deadline. Plaintiff filed a Daubert Motion to Exclude Certain Opinions of

Defendant’s HIV Expert seeking to preclude testimony that the subject HIV test has approval from

any regulatory body. See generally ECF No. [53]. Plaintiff also filed her Motion in Limine seeking

to exclude expert testimony regarding studies and any regulatory approvals as to a rapid HIV test

also produced by the manufacturer of the subject rapid HIV test, but not used on board the Apex.

See ECF No. [54] at 6-11.

Defendant argues that good cause exists for its late filing based upon Plaintiff’s Motions.

Prompted by Plaintiff’s filing, Defendant discovered case law addressing how other courts

consider FDA evidence, its potential effect on jurors, and because the case law may benefit this

Court and conserve juridical resources. ECF No. [82] ¶¶ 5, 6. Defendant argues that the utility of

this case law is good cause for the extension. Id. ¶ 6.

Plaintiff responds that there is no good cause to permit filing the Motion almost one month

past the deadline. ECF No. [84] ¶ 3. Plaintiff asserts that the case law on which Defendant relies

is not only irrelevant but decided in 2020 and therefore was available prior to the Court’s deadline.

Id. ¶¶1, 5.

II. LEGAL STANDARD

“Except in categories of actions exempted by local rule, the district judge [] must issue a

scheduling order” which “may be modified only for good cause and with the judge’s consent.”

Fed. R. Civ. P. 16(b)(1), (4). “Such orders ‘control the subsequent course of the action’. . . and

may be modified only ‘upon a showing of good cause.’” Sosa v. Airprint Systems, Inc., 133 F.3d

1417, 1418 (11th Cir. 1998) (citation omitted). “A party seeking the extension of an already-

expired scheduling order deadline must show both good cause and excusable neglect.” Payne v.

C.R. Bard, Inc., 606 Fed. App’x 940, 944 (11th Cir. 2015) (emphasis in original). “Good cause

exists when the deadline could not ‘be met despite the diligence of the party seeking the

extension.’” Martinez v. Miami Children’s Health Sys., Inc., 2022 WL 17830495, *2, Case No.

21-cv-22700 (S.D. Fla. Dec. 21, 2022) (citation omitted).

III. DISCUSSION

As stated, Defendant seeks to file its Motion out of time. Prompted by issues raised in

Plaintiff’s motions, Defendant argues that it discovered case law indicating that “evidence

pertaining to the FDA and its clearance process is irrelevant and unfairly prejudicial in products

liability cases.” ECF No. [82] ¶ 5. Defendant seeks to argue that a recent decision, Ethicon

Physiomesh Flexible Composite Hernia Mesh Prod. Liab. Litig. V. Ethicon, Inc., 17-MD-2782-

RWS, 2020 WL 9887565 (N.D. Ga. Nov. 25, 2022), applies equally here. Defendant argues that

Ethicon may assist this Court as it offers a basis on how other courts have considered FDA

evidence, the potential effect on jurors, and that deciding this issue at the pre-trial stage will prevent

undue delay during trial and conserve judicial resources. Id. ¶ 6.

Plaintiff responds that the case law Defendant seeks to introduce is “distinguishable and

misleading” and “not on point and irrelevant.” ECF No. [84] ¶¶ 1, 5. Additionally, Plaintiff argues

as the case relied upon was decided in 2020, it was available to Defendant well before this Court’s

deadline. Id. ¶ 5. Plaintiff asks the Court to deny the Motion as Defendant lacks good cause for

the late filing. Id. ¶ 3.

Defendant replies that as Plaintiff did not specifically allege issues on the efficacy of the

rapid test in her Complaint and Defendant did not anticipate FDA evidence would be an issue

while pre-trial motions were filed. ECF No. [90] ¶ 6. Defendant responds that its Motion is

necessary as Plaintiff wishes to introduce an expert report taken on November 8, 2023 — the

deadline for pre-trial motions in limine and Daubert motions — opining that the subject test lacks

FDA approval and cannot be sold in the United States. Id. ¶ 3, 4. Additionally, Defendant responds

that Plaintiff filed motions to preclude Defendant from offering its expert opinions that the

manufacturer of its subject test produces other FDA approved HIV rapid test kits. Id. ¶ 5.

Defendant argues that its Motion is now necessary to show that evidence on the FDA and its

approval processes are “irrelevant and unfairly prejudicial” and should not be admitted before a

jury. Id. ¶ 7.

The Court agrees with Plaintiff that good cause has not been shown. That Defendant

recently found a case decided in 2020 is not a sufficient basis to permit the out of time motion.

Federal Rules of Civil Procedure require district courts to issue scheduling orders. Fed. R. Civ. P.

(b)(1). The party seeking an extension must show that the deadline could not be met despite

diligence on its part. See Sosa v. Airprint Sys., Inc., 133 F.3d 1417, 1418 (11th Cir. 1998) (quoting

Fed. R. Civ. P. 16(b)). Here, an extension for an already expired deadline requires showing both

good cause and excusable neglect.

Defendant argues that it did not anticipate FDA evidence would be an issue at the pre-trial

stage. The Court is unpersuaded by this argument as Plaintiff alleges in her Complaint the

standards Defendant applied for the screening and testing of blood. ECF No. [1] at 5-6, 8, 10-11.

For example, in Count I Plaintiff alleges that Defendant: (d.) “deviated from the applicable

standard of care to screening and testing of blood,” (h.) “[violated] its own policies and procedures

relating to screening and testing of donor blood;” and (j) “[failed] to adequately rapid test the donor

blood for HIV.” Id. ¶ 20. In Count II, Plaintiff alleges that Defendant exercised control over: (l.)

“[d]etermining and selecting the medications, drugs and supplies to be used in the ship’s medical

facility;” and (p.) the staff, equipment, and operations “under the industry Guidelines issued by

the American College of Emergency Physicians and requiring its medical personnel to practice

Case No. 22-cv-22913-BLOOM/Torres

medicine and treat patients in accordance with the requirements of said Guidelines.” /d. § 23. The

efficacy of the test is plainly at issue in the Complaint.

Furthermore, Defendant seeks to introduce its own expert testimony that other rapid HIV

tests produced by the same manufacturer of the subject rapid HIV test it used have FDA approval.

ECF No. [90] §| 7. Defendant fails to address how preparation of its expert opinion testimony

regarding this FDA approval evidence comports with its argument that it did not anticipate FDA

evidence would be an issue at this stage. Accordingly, good cause has not been demonstrated to

warrant this late filing.

In sum, the Court finds that Defendant has failed to demonstrate that the original deadline

could not be met despite diligence on its part. Moreover, the case law Defendant contends is useful

and addresses relevant issues before the Court was available to Defendant to assert well before the

Court’s deadline.

IV. CONCLUSION

Accordingly, it is ORDERED and ADJUDGED as follows:

1. Defendant’s Motion for Leave to File, ECF No. [82], is DENIED.

DONE AND ORDERED in Chambers at Miami, Florida, anuary 26, 2024.

BETH BLOOM

UNITED STATES DISTRICT JUDGE

Copies to:

Counsel of Record

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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