Redick v. Smith & Nephew, Inc.

CourtDistrict Court, D. Maryland
DecidedJanuary 18, 2022
Docket1:17-cv-00944
StatusUnknown

This text of Redick v. Smith & Nephew, Inc. (Redick v. Smith & Nephew, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Redick v. Smith & Nephew, Inc., (D. Md. 2022).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MARYLAND

IN RE: SMITH & NEPHEW BIRMINGHAM MDL No. 2775 HIP RESURFACING Master Docket No. 1:17-md-2775 (BHR) HIP IMPLANT PRODUCTS LIABILITY LITIGATION JUDGE CATHERINE C. BLAKE

THIS DOCUMENT RELATES TO:

Paula and Jace Redick v. Smith & Nephew, Inc., No. 1:17-cv-00944

MEMORANDUM Pending before the court is a motion for new trial in the BHR track case of Paula and Jace Redick v. Smith & Nephew, Inc., No. 1:17-cv-00944. (ECF 751) The Redicks move for a new trial under Fed. R. Civ. P. 59(a)(1)(A). The motion has been fully briefed, and oral argument was heard on October 20, 2021. For the reasons below, the motion will be denied. BACKGROUND & PROCEDURAL HISTORY This case concerns alleged injuries suffered by plaintiffs Paula and Jace Redick as a result of Ms. Redick’s use of the Birmingham Hip Resurfacing Device (“BHR”), an artificial hip implant developed, designed, manufactured, and sold by defendant Smith & Nephew. The BHR replaces the hip joint with metal components—capping the femoral head with a metal covering and inserting a metal cup within the acetabular cup—to recreate the same ball and socket structure that occurs naturally. In re Smith & Nephew Birmingham Hip Resurfacing (BHR) Hip Implant Prod. Liab. Litig. (“In re BHR”), 300 F. Supp. 3d 732, 736 (D. Md. 2018). The friction between the metal components allegedly can cause metal debris to accumulate within the joint and blood stream of the patient. Metal debris from the device can cause pain, metallosis, and other serious complications that may require corrective surgery or revision to a different device. Id. In 2015, Smith & Nephew voluntarily recalled some BHR devices due to unreasonably high rates of failure in women and in men needing femoral head sizes 46 mm or smaller, for reasons including complications due to metal debris. The plaintiffs claim Ms. Redick, a resident of North Carolina,

was one such patient—her BHR implant required revision to a different implant due, in her surgeon’s and expert’s opinions, to symptoms caused by the accumulation of metal debris. The 2021 trial in Ms. Redick’s case ran from July 26 to August 13. After deliberations, the jury returned a verdict in favor of Smith & Nephew. Specifically, applying North Carolina law, the jury found (1) as to breach of express warranty, that no warranty had been made; and (2) as to negligence, that Smith & Nephew had made a false or misleading representation, but Ms. Redick’s surgeon did not justifiably rely on that representation. Accordingly, the jury did not reach the issue of compensatory or punitive damages. (ECF 725, Special Verdict Form). The plaintiffs moved for a new trial on August 24, 2021. (ECF 751). Smith & Nephew responded (ECF 766, 3057), and the Redicks replied (ECF 768, 3125).1 Supplemental briefing was filed in December 2021 following

the deposition of Professor Steven Graves. (ECFs 806, 808). STANDARD OF REVIEW Federal Rule of Civil Procedure 59(a)(1)(A) permits the court to, upon motion, “grant a new trial . . . after a jury trial, for any reason for which a new trial has heretofore been granted in an action at law in federal court.” A court should grant a motion for a new trial only if the verdict is against the clear weight of the evidence, is based on evidence which is false, or will result in a

1 Some documents have multiple docket numbers because they are filed under the Redicks’ individual case and the larger MDL case number. The former (smaller) number will be used to reference such documents throughout this memorandum. Documents with ECF citations in the 2000s to 3000s are filed under 1:17-md-2775; while documents with ECF citations in the 700s and 800s are filed under 1:17-cv-00944. miscarriage of justice. Finch v. Covil Corp., 388 F. Supp. 3d 593, 608 (M.D.N.C. 2019) (citing Bryant v. Aiken Reg'l Med. Ctrs., Inc., 333 F.3d 536, 543 (4th Cir. 2003)). The court may weigh evidence, assess credibility, and exercise its discretion in ruling on a motion for a new trial. Finch, 388 F. Supp. 3d at 608 (citing Cline v. Wal-Mart Stores, Inc., 144 F.3d 294, 301 (4th Cir. 1998)).

A new trial should not be granted unless it is reasonably clear that prejudicial error has occurred or substantial justice has otherwise not been done. Pathways Psychosocial Support Ctr., Inc. v. Town of Leonardtown, 223 F. Supp. 2d 699, 706 (D. Md. 2002) (citing Vanwyk Textile Sys., B.V. v. Zimmer Mach. Am., Inc., 994 F. Supp. 350, 358 (W.D.N.C. 1997)). DISCUSSION The Redicks raise seven arguments in support of granting a new trial, which the court will address sequentially below. I. Testimony of Defense Expert Dr. Michael Mont The plaintiffs first argument for a new trial concerns the trial testimony of Dr. Michael Mont. Specifically, the Redicks contend that:

1) Their case was unfairly prejudiced by Dr. Mont’s undisclosed opinion testimony about what a reasonable orthopedic surgeon knew or should have known at the time of Ms. Redick’s surgery about the risks of the BHR for female patients and those with smaller head sizes; 2) The court’s decision to strike that specific portion of Dr. Mont’s testimony was insufficient to remedy the prejudice it created; and 3) The court’s limitation of the plaintiffs’ cross-examination of Dr. Mont was arbitrary and prejudicial. First, with respect to the portion of Dr. Mont’s contested testimony regarding what a reasonable orthopedic surgeon would have known at the time of Ms. Redick’s surgery, the plaintiffs contend that it came as a surprise so inconsistent with substantial justice as to justify a new trial. See Fed. R. Civ. P. 59(a)(1)(A). They rely on the fact that Dr. Mont’s expert report did

not, as required under Fed. R. Civ. Proc. 26(a)(2)(B), include that specific opinion. As the plaintiffs acknowledge, however, for surprise testimony to require a new trial, the movant must show the surprise is “inconsistent with substantial justice” and resulted in actual prejudice that deprived the party of a fair hearing. (ECF 751-1 at 4-5); Twigg v. Norton Co., 894 F.2d 672, 675 (4th Cir. 1990). a. Dr. Mont’s Relevant Testimony Was Not a Surprise The record does not support the Redicks’ argument that Dr. Mont’s testimony led to actual prejudice to the plaintiffs, nor can much of it fairly be described as any kind of “surprise.” Plaintiffs’ counsel demonstrated their understanding of the gist of Dr. Mont’s testimony at his deposition, asking him: Q. And one of your opinions, I believe, in this case, is that the medical community knew that small femoral head sizes had an increased risk of revision; correct? A. Yes. Q. The medical community knew about that; correct?. . . A. Yes. . . I published it very early, and I talked about it in my conference and people knew about it.

(ECF 766-2 Ex. B, Mont Dep. at 105) Further, as Smith & Nephew points out, the treating surgeon, Dr. Jack Bowling, was allowed to offer undisclosed opinion testimony in his direct examination by plaintiffs’ counsel about what a reasonable surgeon would have wanted to know at the time of Ms. Redick’s surgery. The plaintiffs then declined to call their expert, Dr. Jeffrey Shapiro, whose testimony Dr.

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Redick v. Smith & Nephew, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/redick-v-smith-nephew-inc-mdd-2022.