Shah v. Zimmer Biomet Holdings, Inc.

District Court, N.D. Indiana·Decided September 18, 2020·No. 3:16-cv-00815·Unknown

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF INDIANA SOUTH BEND DIVISION

RAJESH M. SHAH, et al. ) ) Plaintiffs, ) ) vs. ) Case No. 3:16-cv-815-PPS-MGG ) ZIMMER BIOMET HOLDINGS, INC., ) et al., ) ) Defendants. )

OPINION AND ORDER After nearly four years of complex and contested litigation, this securities class action has settled. Before me are Plaintiffs’ Motion for Final Approval of Class Action Settlement and Plan of Allocation [DE 254] and Lead Counsel’s Motion for Award of Attorneys’ Fees and Reimbursement of Litigation Expenses [DE 256.] I previously granted preliminary approval of the settlement and certified a class for settlement purposes. [DE 251; Shah v. Zimmer Biomet Holdings, Inc., 2020 WL 2570050 (N.D. Ind. May 21, 2020).] The parties then sent notice of the settlement to the class and allowed class members to make claims, opt-out, or object to the proposal. On September 3, 2020, I held a telephonic final fairness hearing in which any objectors or other members of the public could attend. I also heard from both plaintiffs’ class counsel and defendants’ counsel. It is clear that the settlement has been well- received by the class, and I stated on the record the reasons why I found the proposed settlement to be plainly fair, adequate and reasonable. This opinion elaborates on those findings and reduces them to writing. It further grants the requested reimbursements of costs and expenses to class counsel and lead plaintiffs. Lastly, while I reserved

judgment on class counsel’s motion for attorneys’ fees at the hearing, I will now grant that motion as well, albeit in part. While I think counsel has done a tremendous job litigating this case on behalf of the class, the requested 33.3% is simply beyond the “market rate” for this case and a reduced percentage fee will be awarded. Background Plaintiffs filed this lawsuit against a multitude of defendants, both corporate and

individual, affiliated with Zimmer Biomet Holdings, Inc. (ZBH for short). ZBH is a multi-billion-dollar medical device manufacturer headquartered in Warsaw, Indiana. It came into existence in June 2015 after two cross-town rivals (Zimmer Holdings, Inc. and Biomet, Inc.) merged with one another. At its core, the complaint alleged that, from June 7, 2016 to November 7, 2016, ZBH and its senior leadership misled investors and

concealed material information from the market in violation of various federal securities laws. Plaintiffs sought to represent a class of all persons who traded in shares of ZBH during the relevant time period and harmed as a result. Although the substance of the complaint is not all that integral to the motions presently before me, it’s worth summarizing what this lawsuit was about, as alleged by

plaintiffs (but of course not admitted to by ZBH). At issue was a major ZBH manufacturing facility known as “North Campus.” By spring 2016, ZBH knew that North Campus was badly out of compliance with federal regulations and has serious issues with its quality systems. ZBH learned this after conducting a series of internal audits. Those audits were conducted in response to systemic regulatory problems with the FDA over non-compliance and quality control issues at a different facility, known as

West Campus, the year before. North Campus was in such a state that it would likely need to be completely overhauled to bring it up to snuff and would likely be shut down in the process. This, of course, would have a dramatic effect on production and thus ZBH’s sales. Plaintiffs allege that given ZBH’s experience with West Campus and other then- recent remediations (specifically one known as “Project Trident”), the company knew

how costly and extensive the remediation of North Campus was going to be and that the FDA had the company under a microscope. Plaintiffs say ZBH was under a duty to disclose the problems at North Campus pursuant to the requirements of Item 303 of SEC Regulation S-K which requires companies to “[d]escribe any known trends or uncertainties that have had or that the registrant reasonably expects will have a material

favorable or unfavorable impact on net sales or revenues or income from continuing operations.” 17 C.F.R. § 229.303(a)(3)(ii). But even knowing what it knew about North Campus, ZBH was issuing investor guidance which contained ambitious revenue and sales targets. Those statements were made during investor calls and conferences, two prospectuses relating to stock offerings

in June and August 2016, and regular SEC filings. Plaintiffs contend that in order to meet the targets the company was announcing and committing itself to, ZBH needed North Campus to be running at full capacity. But full capacity was mutually exclusive with doing the necessary remediation at North Campus. So instead ZBH took a chance, telling the market it was on track to hit its revenue and sales targets and engaging in a few quick-fixes at North Campus in the hopes that everything would work out with

anticipated FDA inspections of North Campus later in 2016. Things didn’t work out as planned. The FDA’s inspection of North Campus began on September 16, 2016 and the issues at North Campus were immediately evident. This led to a complete and almost immediate hold on all products being manufactured out of North Campus. This devasted ZBH’s product supply and therefore its revenue. When ZBH announced its third quarter financial results during an

October 31, 2016 investor call, they weren’t great. The company announced a drop in growth, and it reduced its projected revenue guidance for both the fourth quarter and the year. During the call, ZBH’s CEO stated that the revenue misses were the result of unanticipated supply constraints related to the company’s ongoing efforts to merge its two predecessor entities’ operations. But there was no mention of North Campus’s

problems or the FDA’s ongoing inspection of the facility. Investors and analysts were apparently blindsided by the news, and the company’s stock fell 14%. Plaintiffs allege that the reasons given on the October 31 call were knowingly false and an effort by ZBH to concoct a coverup for the issues at North Campus. Former senior employees at ZBH have stated as much, saying there were directives from the

top to create a different story to explain the company’s performance. Regardless, it didn’t work. In the days following the October 31 investor call, analysts learned of and began reporting on the ongoing FDA inspection at North Campus and the problems being encountered. Plaintiffs say it was this which forced ZBH to finally come clean about its problems.

On November 8, 2016, ZBH disclosed what plaintiffs say were the true cause of the company’s problems in its quarterly SEC filings and a press release. This caused another drop in the company’s stock price. Later that month, much of the scope of the issues were confirmed when the FDA concluded its audit and issued a letter to ZBH which plaintiffs say mirror what ZBH already knew from its own audits. As mentioned, plaintiffs say the concealment of the problems at North Campus were fraudulent

because ZBH had a duty to disclose this information pursuant to Item 303 of SEC Regulation S-K. Plaintiffs further allege that the problems needed to be disclosed because ZBH knew North Campus was going to be audited by the FDA after what had happened at West Campus. They further state that the statements made during the October 31 call were flat out falsehoods.

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Shah v. Zimmer Biomet Holdings, Inc., (N.D. Ind. 2020).

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