Bryan v. C.R. Bard, Inc.

CourtDistrict Court, S.D. Ohio
DecidedJanuary 10, 2024
Docket2:18-cv-01440
StatusUnknown

This text of Bryan v. C.R. Bard, Inc. (Bryan v. C.R. Bard, Inc.) is published on Counsel Stack Legal Research, covering District Court, S.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Bryan v. C.R. Bard, Inc., (S.D. Ohio 2024).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF OHIO EASTERN DIVISION

IN RE: DAVOL, INC./C.R. BARD, Case No. 2:18-md-2846 INC., POLYPROPYLENE HERNIA

MESH PRODUCTS LIABILITY

LITIGATION JUDGE EDMUND A. SARGUS, JR.

Magistrate Judge Kimberly A. Jolson

This document relates to:

Bryan v. C.R. Bard, Inc., et al.

Case No. 2:18-cv-1440

DISCOVERY ORDER

Before the Court is Plaintiff’s Motion to Extend Case-Specific Fact Discovery to Permit Two Limited, Case-Specific Depositions (ECF Nos. 42, 54). Defendants oppose Plaintiff’s Motion. (ECF Nos. 44, 55.) For the reasons that follow, Plaintiff’s Motion is DENIED. I. Background Plaintiff’s case is the fourth bellwether trial selected from thousands of cases in this multidistrict litigation (“MDL”) against Defendants. The Judicial Panel on Multidistrict Litigation described the cases in this MDL as “shar[ing] common factual questions arising out of allegations that defects in defendants’ polypropylene hernia mesh products can lead to complications when implanted in patients, including adhesions, damage to organs, inflammatory and allergic responses, foreign body rejection, migration of the mesh, and infections.” (No. 2:18-md-02846, ECF No. 1 at PageID #1–2.) The relevant facts here are that in 2012, Plaintiff underwent an inguinal hernia repair with a 3DMax hernia mesh device, a product manufactured by Defendants. (ECF No. 1 at PageID #3.) In 2017, Plaintiff underwent a surgical removal of the 3DMax. (Id.) The crux of Plaintiff’s claims is that Defendants knew of certain risks presented by the 3DMax but marketed and sold the device despite these risks and without appropriate warnings, causing Plaintiff’s injuries. Plaintiff filed a motion seeking to depose two of Defendants’ sales representatives, Austin Knipp and Brad Prouty, after the close of fact discovery. (ECF No. 42.) In their response Defendants pointed out that, as was noted on their Defendants’ Fact Sheet (“DFS”) which they served to Plaintiff in 2019, Knipp

and Prouty were not employed with Defendants until years after Plaintiff’s implant surgery. (ECF No. 44 at PageID #233.) Plaintiff filed an amended motion adopting his prior arguments but swapping Knipp and Prouty out for two different former employees, Andrew O’Keefe and Matt Fenton. (ECF No. 54.) II. Legal Standard A scheduling order “may be modified only for good cause and with the judge’s consent.” Fed. R. Civ. P. 16(b)(4). Factors that should be considered include: (1) When the moving party learned of the issue that is the subject of discovery; (2) How the discovery would affect the [case]; (3) The length of the discovery period; (4) Whether the moving party was dilatory; and (5) Whether the adverse party was responsive to prior discovery requests.

Dowling v. Cleveland Clinic Found., 593 F.3d 472, 478 (6th Cir. 2010). “The overarching inquiry in these overlapping factors is whether the moving party was diligent in pursuing discovery.” Id. A court should also consider any potential prejudice to the opposing party. Andretti v. Borla Performance Indus., Inc., 426 F.3d 824, 830 (6th Cir. 2005) (citing Inge v. Rock Fin. Corp., 281 F.3d 613, 625 (6th Cir.2002)). III. Analysis A. When Plaintiff Learned of the Issue The parties frame this factor differently. Plaintiff appears to believe that the factor refers not to when Plaintiff learned of the employees’ identities, but to when Plaintiff sought the depositions. Plaintiff claims he is “raising this issue immediately upon learning about the Defendants’ refusal to agree to these requested depositions and after the required meet and confer.” (ECF No. 42 at PageID #208.) However, Defendants point out that Plaintiff learned of the identity of the employees over four years ago. (ECF No. 44 at PageID #234.) The second page of the

DFS, which was served on April 25, 2019, lists O’Keefe and other sales representatives and their dates of employment. (ECF No. 44-1 at PageID #241.) The DFS does not mention Fenton, who Plaintiff never alleges had contact with Dr. Caban but who supervised O’Keefe and a now-deceased former sales representative, Bruce Speers. (Id.) The Court agrees with Defendants’ interpretation of this factor. Plaintiff has known the names and dates of employment of four sales representatives since 2019, and did not seek any depositions until November 22, 2023, approximately one month after the close of fact discovery. This factor weighs in favor of denying Plaintiff’s Motion. B. How Discovery Would Affect the Case Plaintiff argues that the depositions of the sales representatives “are critical for obtaining

information regarding the messages and safety information that w[ere] shared (or not shared) with Plaintiff’s implanting physician,” and the depositions are therefore critical to his “failure to warn and other claims.” (ECF No. 42 at PageID #208.) In his amended Motion seeking to depose O’Keefe and Fenton, Plaintiff claims that “the names of the deposition witnesses to testify on this important topic are fungible” and although the names of the witnesses have changed, the substance of his request has not. (ECF No. 54 at PageID #270.) The Court disagrees. Unlike the sales representatives Plaintiff initially sought to depose, Dr. Caban was not questioned about and did not himself mention O’Keefe nor Fenton during his deposition. Fenton was a supervisor and Plaintiff never contends that he interacted with Dr. Caban. In seeking to depose Fenton, Plaintiff points out that Fenton supervised now-deceased sales representative Speers “who detailed Dr. Caban from 1999 to 2011.” (ECF No. 54 at PageID #268.) However, in his deposition Dr. Caban specifically testified that he did not recall the name Bruce Speers. (ECF No. 42-1 at PageID #214–15, 21:24–22:2.) And “[w]hile Dr. Caban did

testify that certain reps contacted him prior to 2012, neither [O’Keefe] nor [Fenton] was identified as one of those reps.” (ECF No. 44 at PageID #234.) Plaintiff claims the depositions are important so he can learn “the number of times that a sales representative sat in on a 3DMax surgery prior to [Plaintiff]’s implant.” (ECF No. 54 at PageID #270.) However, Plaintiff does not explain how this would be relevant to his claims. Plaintiff claims that these depositions would also cover “interactions and discussions related to the 3DMax; what brochures and marketing materials [Plaintiff’s] treating physicians received; whether the sales representatives were involved in any training sessions with [Plaintiff’s] physicians; as well as the medical literature the sales-related witnesses distributed or referenced during conversations with [Plaintiff’s] treating physicians.” (Id. at PageID #270–71.) However,

Dr. Caban testified that he based his decisions on “[his] own training, not on what any rep will say. . . . So whatever influence the rep has, it has absolutely zero influence in [his] clinical decisions.” (ECF No. 55-1 at PageID #296, 26:12–20.) And while sales representatives would discuss with him the benefits of using their products, he “d[id not] use the product just because they say that” and “d[id not] base [his] practice on what a rep tells [him] or what the company tells [him].” (Id. at PageID #295, 24:4–12; #310 at 85:14–15.) Plaintiff claims that Dr. Caban spoke with Defendants’ sales representatives once a month from 2006 until the time of his deposition, therefore these witnesses will have “extremely probative information about what was provided to Dr. Caban and what was discussed with him for the entire time he was practicing.” (ECF No. 54 at PageID #269.) However, Dr. Caban did not testify that he spoke that frequently with Defendants’ sales representatives specifically.

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Related

Dowling v. Cleveland Clinic Foundation
593 F.3d 472 (Sixth Circuit, 2010)

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