In re Zimmer Biomet Holdings, Inc. Derivative Litigation
Opinion
IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE
IN RE ZIMMER BIOMET HOLDINGS, ) CONSOLIDATED INC. DERIVATIVE LITIGATION ) C.A. No. 2019-0455-LWW
MEMORANDUM OPINION Date Submitted: June 15, 2021 Date Decided: August 25, 2021
P. Bradford deLeeuw, DELEEUW LAW LLC, Wilmington, Delaware; Richard A. Speirs and Christopher Lometti, COHEN MILSTEIN SELLERS & TOLL PLLC, New York, New York; Robert C. Schubert, Willem F. Jonckheer, SCHUBERT JONCKHEER & KOLBE LLP, San Francisco, California; Kip B. Shuman, SHUMAN, GLEEN & STECKER, San Francisco, California; Rusty E. Glenn, SHUMAN, GLEEN & STECKER, Denver, Colorado; Brett D. Stecker, SHUMAN, GLEEN & STECKER, Ardmore, Pennsylvania; Counsel for Plaintiffs Jody C. Barillare, MORGAN, LEWIS & BOCKIUS LLP, Wilmington, Delaware; Troy S. Brown, Laura Hughes McNally, Brian F. Morris, and Karen Pieslak Pohlmann, MORGAN, LEWIS & BOCKIUS LLP, Philadelphia, Pennsylvania; Counsel for Defendants Zimmer Biomet Holdings, Inc., Christopher B. Begley, Betsy J. Bernard, Paul M. Bisaro, Gail K. Boudreaux, Tony W. Collins, David C. Dvorak, Michael J. Farrell, Daniel P. Florin, Larry Glasscock, Robert A. Hagemann, Arthur J. Higgins, Robert J. Marshall Jr., and Cecil B. Pickett, Ph.D. William M. Lafferty, Ryan D. Stottmann, and Sabrina M. Hendershot, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Peter E. Kazanoff, Sara A. Ricciardi, and Courtney G. Skarupski, SIMPSON THACHER & BARTLETT LLP, New York, New York; Counsel for Defendants Michael W. Michelson and KKR Biomet, LLC
William M. Lafferty, Ryan D. Stottmann, and Sabrina M. Hendershot, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Daniel V. McCaughey and Erin Macgowan, ROPES & GRAY LLP, Boston, Massachusetts; Christian Reigstad, ROPES & GRAY LLP, New York, New York; Counsel for Defendants Jeffrey K. Rhodes, TPG Partners IV, L.P., TPG Partners V, L.P., TPG FOF V-A L.P., TPG FOF V-B, L.P., TPG LVB Co-Invest LLC, and TPG LVB Co- Invest II LLC
Daniel A. Mason and Matthew D. Stachel, PAUL, WEISS, RIFKIND, WHARTON & GARRISON LLP, Wilmington, Delaware; Andrew J. Ehrlich and Brette Tannenbaum, PAUL, WEISS, RIFKIND, WHARTON & GARRISON LLP, New York, New York; Counsel for Defendants Blackstone Capital Partners V L.P., Blackstone Capital Partners V-AC L.P., Blackstone BCP V-S L.P., Blackstone Family Investment Partnership V L.P., Blackstone Family Investment Partnership V-SMD L.P., Blackstone Participation Partnership V L.P., and BCP V CoInvestors L.P.
Kevin G. Abrams and J. Peter Shindel, Jr., ABRAMS & BAYLISS LLP, Wilmington, Delaware; Paul Vizcarrondo and John F. Lynch, WACHTELL, LIPTON, ROSEN & KATZ, New York, New York; Counsel for Defendants GS Capital Partners VI Fund, L.P., GS Capital Partners VI Parallel, L.P., GS Capital Partners VI Offshore Fund, L.P., GS Capital Partners VI GmbH & Co. KG, Goldman Sachs BMET Investors, L.P., Goldman Sachs BMET Investors Offshore Holdings, L.P., PEP Bass Holdings, LLC, Private Equity Partners 2004 Direct Investment Fund, L.P., Private Equity Partners 2005 Direct L.P., Private Equity Partners IX Direct L.P., and Goldman Sachs LVB Co-Invest, L.P.
WILL, Vice Chancellor
This is a derivative suit brought by stockholders of Zimmer Biomet Holdings,
Inc., a company that manufactures and markets various products in the highly
regulated medical device industry. The plaintiffs’ claims stem from a September 12,
2016 “for cause” inspection of Zimmer’s North Campus site in Warsaw, Indiana by
the U.S. Food & Drug Administration. The compliance problems identified during
that inspection resulted in Zimmer issuing a blanket hold on shipments of products
processed at the North Campus facility. Zimmer subsequently reported
disappointing financial results for the third quarter of 2016, reduced its fourth quarter
guidance, and saw its stock price fall 14%.
After outside analysts reported on the results of the FDA’s North Campus
inspection, a federal securities action and this litigation followed. In this matter, the
plaintiffs seek to pursue derivative claims for breach of fiduciary duty, insider
trading, unjust enrichment, and breach of contract. These claims are brought against
current and former officers and directors of Zimmer and against multiple entities that
sold Zimmer stock in three registered offerings in 2016. The primary theory behind
the plaintiffs’ claims is that Zimmer’s officers and directors knew in 2015 and 2016
that Zimmer was facing serious regulatory compliance challenges but concealed
them from the market while facilitating sales of Zimmer stock by private equity
funds in possession of that material non-public information.
The defendants have moved to dismiss the complaint for failure to adequately
plead demand futility and for failure to state a claim. I conclude that those motions
must be granted. As with many derivative actions, a threshold issue in this case is
whether the plaintiffs’ failure to make a pre-suit demand on the Zimmer board is
excused. Of the eleven-member board in place when this lawsuit was filed, the
plaintiffs acknowledge that eight directors were independent, received no special
benefit from the challenged trades, and had no ties to the private equity funds that
traded. They argue that making a demand would nonetheless have been futile
because a majority of those directors face a substantial likelihood of liability.
The plaintiffs have not alleged particularized facts to support that argument.
Zimmer has an exculpation provision in its charter, meaning that the plaintiffs must
plead facts suggesting a fair inference that the directors breached their duty of
loyalty. The plaintiffs’ complaint details a host of compliance violations—large and
small—at multiple Zimmer facilities from China to Puerto Rico to Indiana, along
with various remediation efforts Zimmer took throughout 2015 and 2016. But the
plaintiffs point to nothing until late 2016 that would have alerted a majority of the
directors to an imminent product ship hold at the North Campus and resulting
financial implications. By then, the secondary offerings had been completed. In
terms of disclosures, the plaintiffs cannot link what the Zimmer board knew before
late 2016 to any material misstatements or omissions that the board was directly
involved in issuing. After the ship holds began in September 2016, the plaintiffs—
at most—connect the four Audit Committee members to an earnings release that
reduced guidance but cannot support a duty of loyalty claim against those directors.
At bottom, the plaintiffs cannot show that a majority of the board faces a
substantial likelihood of liability for non-exculpated claims. There are no specific
facts pleaded to support a reasonable inference that the directors acted in bad faith,
intentionally concealed material information, knowingly facilitated insider trading,
or deliberately ignored “red flags.” Because the plaintiffs cannot demonstrate that
the board’s capacity for impartiality was compromised, demand is not excused as
futile. This case is dismissed in its entirety under Court of Chancery Rule 23.1.
I. FACTUAL BACKGROUND
The following facts are drawn from the Verified Consolidated Stockholder
Derivative Complaint (the “Complaint”) and the documents it incorporates by
reference.1
1 Verified Consolidated S’holder Deriv. Compl. (“Compl.”) (Dkt. 47). See Winshall v. Viacom Int’l, Inc., 76 A.3d 808, 818 (Del. 2013) (“[A] plaintiff may not reference certain documents outside the complaint and at the same time prevent the court from considering those documents’ actual terms.”); Freedman v. Adams, 2012 WL 1345638, at *5 (Del. Ch. Mar. 30, 2012) (“When a plaintiff expressly refers to and heavily relies upon documents in her complaint, these documents are considered to be incorporated by reference into the complaint . . . .”). The parties agreed that documents produced by Zimmer pursuant to 8 Del. C. § 220 would be deemed incorporated into any complaint the plaintiffs filed. See Amalgamated Bank v. Yahoo! Inc., 132 A.3d 752, 797 (Del. Ch. 2016).
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IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE
IN RE ZIMMER BIOMET HOLDINGS, ) CONSOLIDATED INC. DERIVATIVE LITIGATION ) C.A. No. 2019-0455-LWW
MEMORANDUM OPINION Date Submitted: June 15, 2021 Date Decided: August 25, 2021
P. Bradford deLeeuw, DELEEUW LAW LLC, Wilmington, Delaware; Richard A. Speirs and Christopher Lometti, COHEN MILSTEIN SELLERS & TOLL PLLC, New York, New York; Robert C. Schubert, Willem F. Jonckheer, SCHUBERT JONCKHEER & KOLBE LLP, San Francisco, California; Kip B. Shuman, SHUMAN, GLEEN & STECKER, San Francisco, California; Rusty E. Glenn, SHUMAN, GLEEN & STECKER, Denver, Colorado; Brett D. Stecker, SHUMAN, GLEEN & STECKER, Ardmore, Pennsylvania; Counsel for Plaintiffs Jody C. Barillare, MORGAN, LEWIS & BOCKIUS LLP, Wilmington, Delaware; Troy S. Brown, Laura Hughes McNally, Brian F. Morris, and Karen Pieslak Pohlmann, MORGAN, LEWIS & BOCKIUS LLP, Philadelphia, Pennsylvania; Counsel for Defendants Zimmer Biomet Holdings, Inc., Christopher B. Begley, Betsy J. Bernard, Paul M. Bisaro, Gail K. Boudreaux, Tony W. Collins, David C. Dvorak, Michael J. Farrell, Daniel P. Florin, Larry Glasscock, Robert A. Hagemann, Arthur J. Higgins, Robert J. Marshall Jr., and Cecil B. Pickett, Ph.D. William M. Lafferty, Ryan D. Stottmann, and Sabrina M. Hendershot, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Peter E. Kazanoff, Sara A. Ricciardi, and Courtney G. Skarupski, SIMPSON THACHER & BARTLETT LLP, New York, New York; Counsel for Defendants Michael W. Michelson and KKR Biomet, LLC
William M. Lafferty, Ryan D. Stottmann, and Sabrina M. Hendershot, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Daniel V. McCaughey and Erin Macgowan, ROPES & GRAY LLP, Boston, Massachusetts; Christian Reigstad, ROPES & GRAY LLP, New York, New York; Counsel for Defendants Jeffrey K. Rhodes, TPG Partners IV, L.P., TPG Partners V, L.P., TPG FOF V-A L.P., TPG FOF V-B, L.P., TPG LVB Co-Invest LLC, and TPG LVB Co- Invest II LLC
Daniel A. Mason and Matthew D. Stachel, PAUL, WEISS, RIFKIND, WHARTON & GARRISON LLP, Wilmington, Delaware; Andrew J. Ehrlich and Brette Tannenbaum, PAUL, WEISS, RIFKIND, WHARTON & GARRISON LLP, New York, New York; Counsel for Defendants Blackstone Capital Partners V L.P., Blackstone Capital Partners V-AC L.P., Blackstone BCP V-S L.P., Blackstone Family Investment Partnership V L.P., Blackstone Family Investment Partnership V-SMD L.P., Blackstone Participation Partnership V L.P., and BCP V CoInvestors L.P.
Kevin G. Abrams and J. Peter Shindel, Jr., ABRAMS & BAYLISS LLP, Wilmington, Delaware; Paul Vizcarrondo and John F. Lynch, WACHTELL, LIPTON, ROSEN & KATZ, New York, New York; Counsel for Defendants GS Capital Partners VI Fund, L.P., GS Capital Partners VI Parallel, L.P., GS Capital Partners VI Offshore Fund, L.P., GS Capital Partners VI GmbH & Co. KG, Goldman Sachs BMET Investors, L.P., Goldman Sachs BMET Investors Offshore Holdings, L.P., PEP Bass Holdings, LLC, Private Equity Partners 2004 Direct Investment Fund, L.P., Private Equity Partners 2005 Direct L.P., Private Equity Partners IX Direct L.P., and Goldman Sachs LVB Co-Invest, L.P.
WILL, Vice Chancellor
This is a derivative suit brought by stockholders of Zimmer Biomet Holdings,
Inc., a company that manufactures and markets various products in the highly
regulated medical device industry. The plaintiffs’ claims stem from a September 12,
2016 “for cause” inspection of Zimmer’s North Campus site in Warsaw, Indiana by
the U.S. Food & Drug Administration. The compliance problems identified during
that inspection resulted in Zimmer issuing a blanket hold on shipments of products
processed at the North Campus facility. Zimmer subsequently reported
disappointing financial results for the third quarter of 2016, reduced its fourth quarter
guidance, and saw its stock price fall 14%.
After outside analysts reported on the results of the FDA’s North Campus
inspection, a federal securities action and this litigation followed. In this matter, the
plaintiffs seek to pursue derivative claims for breach of fiduciary duty, insider
trading, unjust enrichment, and breach of contract. These claims are brought against
current and former officers and directors of Zimmer and against multiple entities that
sold Zimmer stock in three registered offerings in 2016. The primary theory behind
the plaintiffs’ claims is that Zimmer’s officers and directors knew in 2015 and 2016
that Zimmer was facing serious regulatory compliance challenges but concealed
them from the market while facilitating sales of Zimmer stock by private equity
funds in possession of that material non-public information.
The defendants have moved to dismiss the complaint for failure to adequately
plead demand futility and for failure to state a claim. I conclude that those motions
must be granted. As with many derivative actions, a threshold issue in this case is
whether the plaintiffs’ failure to make a pre-suit demand on the Zimmer board is
excused. Of the eleven-member board in place when this lawsuit was filed, the
plaintiffs acknowledge that eight directors were independent, received no special
benefit from the challenged trades, and had no ties to the private equity funds that
traded. They argue that making a demand would nonetheless have been futile
because a majority of those directors face a substantial likelihood of liability.
The plaintiffs have not alleged particularized facts to support that argument.
Zimmer has an exculpation provision in its charter, meaning that the plaintiffs must
plead facts suggesting a fair inference that the directors breached their duty of
loyalty. The plaintiffs’ complaint details a host of compliance violations—large and
small—at multiple Zimmer facilities from China to Puerto Rico to Indiana, along
with various remediation efforts Zimmer took throughout 2015 and 2016. But the
plaintiffs point to nothing until late 2016 that would have alerted a majority of the
directors to an imminent product ship hold at the North Campus and resulting
financial implications. By then, the secondary offerings had been completed. In
terms of disclosures, the plaintiffs cannot link what the Zimmer board knew before
late 2016 to any material misstatements or omissions that the board was directly
involved in issuing. After the ship holds began in September 2016, the plaintiffs—
at most—connect the four Audit Committee members to an earnings release that
reduced guidance but cannot support a duty of loyalty claim against those directors.
At bottom, the plaintiffs cannot show that a majority of the board faces a
substantial likelihood of liability for non-exculpated claims. There are no specific
facts pleaded to support a reasonable inference that the directors acted in bad faith,
intentionally concealed material information, knowingly facilitated insider trading,
or deliberately ignored “red flags.” Because the plaintiffs cannot demonstrate that
the board’s capacity for impartiality was compromised, demand is not excused as
futile. This case is dismissed in its entirety under Court of Chancery Rule 23.1.
I. FACTUAL BACKGROUND
The following facts are drawn from the Verified Consolidated Stockholder
Derivative Complaint (the “Complaint”) and the documents it incorporates by
reference.1
1 Verified Consolidated S’holder Deriv. Compl. (“Compl.”) (Dkt. 47). See Winshall v. Viacom Int’l, Inc., 76 A.3d 808, 818 (Del. 2013) (“[A] plaintiff may not reference certain documents outside the complaint and at the same time prevent the court from considering those documents’ actual terms.”); Freedman v. Adams, 2012 WL 1345638, at *5 (Del. Ch. Mar. 30, 2012) (“When a plaintiff expressly refers to and heavily relies upon documents in her complaint, these documents are considered to be incorporated by reference into the complaint . . . .”). The parties agreed that documents produced by Zimmer pursuant to 8 Del. C. § 220 would be deemed incorporated into any complaint the plaintiffs filed. See Amalgamated Bank v. Yahoo! Inc., 132 A.3d 752, 797 (Del. Ch. 2016).
A. Zimmer’s Business, Board, and the PE Funds
Nominal defendant Zimmer Biomet Holdings, Inc. (“Zimmer” or the
“Company”) designs, manufactures, and markets a variety of medical devices
throughout the world.2 Because Zimmer’s products are “medical devices” under the
Food, Drug, and Cosmetic Act, it is regulated by the U.S. Food & Drug
Administration.3 Zimmer’s products include “Class III” medical devices (such as
implantable orthopedic devices used for knee, hip, and spine treatments), which are
subject to intense FDA scrutiny.4
The Company, as it exists today, was formed through Zimmer Holdings, Inc.’s
(“Legacy Zimmer”) acquisition of Biomet, Inc. (“Legacy Biomet”) on June 24, 2015
for cash and stock consideration totaling nearly $15 billion.5 Before the merger,
Legacy Biomet was 97% owned6 by funds affiliated with The Blackstone Group,7
2 Compl. ¶ 2.
3 Id. ¶ 91.
4 See id. ¶ 93.
5 Id. ¶ 82.
6 Id. ¶ 4.
7 The defendant funds associated with The Blackstone Group are: Blackstone Capital Partners V L.P., Blackstone Capital Partners V-AC L.P., BCP V-S L.P., Blackstone Family Investment Partnership V L.P., Blackstone Family Investment Partnership V-SMD L.P., Blackstone Participation Partnership V L.P., and BCP V Co-Investors L.P. See id. ¶¶ 48– 49. Those entities are referred to collectively as the “Blackstone Funds.”
Goldman Sachs Capital Partners,8 Kohlberg Kravis Roberts & Co. L.P.,9 and TPG
Global, LLC.10 That group of private equity funds will be referred to as the “PE
Funds.” After the merger, the PE Funds held about 15% of Zimmer’s publicly traded
common stock.11
Zimmer entered into an April 14, 2014 Stockholders Agreement with Legacy
Biomet’s holding company (LVB Acquisition Holding, LLC) in connection with the
merger.12 The Stockholders Agreement provides that the PE Funds could require
Zimmer to register its securities, enabling the PE Funds to sell their holdings in
future public offerings subject to restrictions.13
8 The defendant funds associated with Goldman Sachs Capital Partners are: GS Capital Partners VI Fund, L.P., GS Capital Partners VI GmbH & Co. KG, GS Capital Partners VI Offshore Fund, L.P., GS Capital Partners VI Parallel, L.P., GS LVB Co-Invest, L.P., Goldman Sachs BMET Investors, L.P., Goldman Sachs BMET Investors Offshore Holdings, L.P., PEP Bass Holdings, LLC, Private Equity Partners 2004 Direct Investment Fund L.P., Private Equity Partners 2005 Direct L.P., and Private Equity Partners IX Direct L.P. See id. ¶¶ 52–53. Those entities are referred to collectively as the “Goldman Funds.” 9 Defendant KKR Biomet LLC (the “KKR Fund”) is an affiliate of Kohlberg Kravis Roberts & Co L.P. Id. ¶¶ 56–57. 10 The defendant funds associated with TPG Global, LLC are: TPG Partners IV, L.P., TPG Partners V, L.P., TPG FOF V-A, L.P., TPG FOF V-B, L.P., TPG LVB Co-Invest LLC, and TPG LVB Co-Invest II LLC. See id. ¶¶ 59–60. Those entities are referred to collectively as the “TPG Funds.” 11 Id. ¶¶ 4, 84.
Stachel Decl. Ex. 1 (“Stockholders Agreement”), as amended March 30, 2015 (Dkt. 71); 12
Compl. ¶ 371. 13 Stockholders Agreement §§ 4.1, 4.3.
The Stockholders Agreement also allowed the PE Funds to nominate two
directors to Zimmer’s board of directors (the “Board”).14 The PE Funds nominated
defendants Jeffrey K. Rhodes (an affiliate of the TPG Funds) and Michael W.
Michelson (an affiliate of the KKR Fund).15 The Stockholders Agreement permitted
Michelson and Rhodes to share certain non-public information about Zimmer with
the PE Funds:16
Notwithstanding anything to the contrary herein, without limiting any such Principal Stockholder Director’s fiduciary duties under Applicable Law, each of the parties hereto hereby consents to each Principal Stockholder Director sharing any information such Principal Stockholder Director (in his or her capacity as such) receives from the Company with the respective officers, directors, members, employees, attorneys, accountants, consultants, bankers and financial advisors of any Sponsor [PE Fund] . . . .17
The plaintiffs allege that defendants Rhodes and Michelson used their Board
positions to engage in insider trading. Rhodes left the Board in 2017, before this
litigation was filed.18 Of the 11 directors on the Board when this suit commenced,
just three—defendants Michelson and Arthur J. Higgins (an affiliate of Blackstone)
14 Compl. ¶ 85; Stockholders Agreement § 1.1 (“On or prior to the Closing Date, (i) the Company’s board of directors (the “Board”) shall take all action necessary and appropriate . . . to cause the number of directors on the Board to be increased by two (2) and (ii) the Board shall appoint two individuals selected by the [PE Funds].”). 15 Compl. ¶¶ 85, 87.
16 Id. ¶ 85.
17 Stockholders Agreement § 1.6(b); see also id. § 1.7.
18 Compl. ¶ 45.
and non-party Brian Hanson (Zimmer’s CEO)—purportedly lack independence.19
The remaining eight directors on the Board at that time—Christopher B. Begley,
Betsey J. Bernard, Gail K. Boudreaux, Michael J. Farrell, Larry C. Glasscock, and
Robert A. Hagemann (together, the “Director Defendants”), and non-parties Syed
Jafry and Maria Hilado20—are outside directors with no alleged ties to the PE Funds.
Two other former directors—Paul M. Bisaro and Cecil B. Pickett—are also
defendants but left the Board before this litigation was filed.21
The Complaint also names as defendants two of Zimmer’s former executive
officers. David C. Dvorak was Zimmer’s Chief Executive Officer, President, and a
member of the Board.22 Defendant Daniel P. Florin was Zimmer’s Chief Financial
Officer until his resignation.23 Dvorak and Florin left Zimmer in 2017 and 2019,
respectively.24
19 Compl. ¶¶ 294 n.29, 326.
20 Id. ¶¶ 35–42, 294.
21 Id. ¶¶ 43–44.
22 Id. ¶ 33.
23 Id. ¶ 34.
24 Id. ¶¶ 33–34. The Complaint also, at times, lists “Collins” as a defendant. See, e.g., id. ¶¶ 133, 140, 151. The plaintiffs appear to be referencing Tony W. Collins, Zimmer’s Vice President, Corporate Controller, and Chief Accounting Officer during the relevant time period. He is not included in the “Parties” section of the Complaint and there are no substantive allegations about him.
B. The PE Funds Exit Their Investments in 2016.
On February 4, 2016, consistent with the Stockholders Agreement, Zimmer
filed a Form S-3 shelf Registration Statement for planned public stock offerings by
the PE Funds.25 Zimmer’s directors, including Michelson and Rhodes, signed the
Registration Statement.26 Three public secondary offerings pursuant to the
Registration Statement followed.
First, on February 10, 2016, the Blackstone Funds sold the entirety of their
Zimmer holdings and the Goldman Funds sold about half of their Zimmer
investment (the “February Offering”).27 In total, the Blackstone Funds and Goldman
Funds received proceeds of approximately $1.06 billion from the February
Offering.28 Zimmer issued a preliminary prospectus supplement in connection with
that February Offering on February 5, 2016 and a final prospectus supplement on
February 8, 2016.29
Then, in a June 13, 2016 public offering, the TPG Funds and KKR Fund sold
about half of their remaining Zimmer shares and the Goldman Funds sold the rest of
25 Id. ¶¶ 215, 260; see Stockholders Agreement § 4.3.
26 See Compl. ¶¶ 42, 45, 260. Specifically, Begley, Bernard, Bisaro, Boudreaux, Dvorak, Farrell, Florin, Glasscock, Hagemann, Higgins, Michelson, Pickett, and Rhodes each signed the Registration Statement. Id. ¶¶ 33–45, 260. 27 Id. ¶ 261.
28 Id. The Blackstone Funds sold 7,351,708 shares in the offering at $95.91 per share. Id. The Goldman Funds sold 3,675,850 shares of Zimmer stock at $96.66 per share. Id. 29 Id. ¶ 260.
their stake (the “June Offering”).30 For that June Offering, Zimmer supplemented
the Registration Statement with a preliminary prospectus supplement on June 13,
2016 and a final prospectus supplement on June 15, 2016.31
Finally, in a third public offering on August 9, 2016, the TPG Funds and KKR
Fund each sold their remaining Zimmer shares (the “August Offering”).32 The
August Offering was also conducted pursuant to the Registration Statement.
Zimmer supplemented the Registration Statement with a preliminary prospectus
supplement on August 9, 2016 and a final prospectus supplement on August 11,
2016.33 As of August 9, 2016, the PE Funds were no longer invested in Zimmer.
C. The FDA’s Ongoing Monitoring and Inspection of Zimmer
The plaintiffs challenge the February, June, and August Offerings because,
they contend, those offerings were conducted at a time when the PE Funds had
material non-public information obtained through Michelson and Rhodes.34 They
30 Id. ¶ 262. The TPG Funds sold 3,675,855 shares—50% of its interest in the Company— at $115.31 per share, netting proceeds of roughly $424 million. Id. The KKR Fund sold 3,764,820 shares—50% of its interest in the Company—for $115.31 per share, netting proceeds of about $434 million. Id. And the Goldman Funds sold their remaining 3,675,858 Zimmer shares at $115.31 per share, also netting proceeds of approximately $424 million. Id. 31 Id. ¶ 263.
32 Id. ¶ 264. KKR Biomet sold its 3,764,820 shares at $129.00 per share, netting proceeds of roughly $486 million. Id. The TPG Funds sold their remaining 3,675,855 shares of Zimmer stock at $129.00 per share, netting proceeds of about $474 million. Id. 33 Id. ¶ 265.
34 See, e.g., id. ¶¶ 1, 90, 250, 271.
allege that the Board, including Michelson and Rhodes—and thus the PE Funds—
knew that Zimmer was facing a series of regulatory challenges that were hidden from
the market at the time of the Offerings.
As a manufacturer of “Class II” and “Class III” medical devices, Zimmer is
subject to biennial FDA inspections.35 The FDA is also authorized to conduct pre-
approval, compliance follow-up, and “for cause” inspections.36 If an inspection
reveals regulatory violations, FDA inspectors may identify them in a written report
known as a “Form 483.”37 A company that receives a Form 483 generally responds
to the FDA within fifteen days with a comprehensive plan to remedy the
deficiencies.38 If the violations are not addressed, the FDA may issue a “Warning
Letter” that details the continued violations and gives the company a set amount of
time to address them before further action is taken.39 Receipt of a Warning Letter
means that an offending facility can no longer obtain premarket approval on new
35 Id. ¶ 93.
36 Id. ¶ 94.
37 See FDA Form 483 Frequently Asked Questions, U.S. Food & Drug Admin. (Jan. 9, 2020), https://www.fda.gov/inspections-compliance-enforcement-and-criminalinvestigations /inspection-references/fda-form-483-frequently-asked-questions (explaining that a Form 483 “is issued to firm management at the conclusion of an inspection when an investigator(s) has observed any conditions that in their judgment may constitute violations of the [FDCA] and related Acts”); Compl. ¶ 97. 38 Compl. ¶ 103.
39 Id.
Class III medical devices until the observations are remediated.40 The FDA may
take more drastic actions, such as issuing a “Consent Decree,” where serious
concerns are unremedied.41 A “rare consequence” of an FDA inspection is a product
ship hold.42
Both before and after the merger, various Zimmer facilities around the world
were the recipients of Form 483s and Warning Letters that outlined negative
observations. The Board received “detailed regular reports . . . that include[d]
discussions of the risks and exposures” concerning FDA-enforced laws and
regulations.43 Board meetings often included a discussion of FDA compliance
efforts and the results of both internal audits and FDA investigations.
For example, at the first Board meeting held post-merger on July 17, 2015,
the Board received a presentation called “FDA and Project Trident Update.”44 The
presentation described an ongoing FDA compliance remediation program called
“Project Trident” in place at several Legacy Zimmer facilities.45 The presentation
40 Id.
41 Id. ¶ 104.
42 Id. ¶ 19.
43 Id. ¶ 8.
44 Id. ¶¶ 127–28.
45 The facilities involved in Project Trident included those located in Warsaw, Indiana; Ponce, Puerto Rico; Parsippany, New Jersey; and Winterthur, Switzerland. Id. ¶ 128. The plaintiffs allege that as of September 2015, Project Trident had cost Zimmer nearly $250 million. Id. ¶¶ 128, 138.
identified the “[s]uccessful FDA re-inspections” at Zimmer’s West Campus facility
in Warsaw, Indiana and the Company’s Ponce, Puerto Rico facility as a top priority
for 2015.46 Both facilities had been issued Form 483s (identifying 12 deficiencies
at the West Campus facility and nine deficiencies at the Ponce facility, respectively)
after FDA inspections in 2014.47 The presentation noted that Zimmer’s North
Campus location—the facility central to the plaintiffs’ allegations given its role
manufacturing crucial products—had also been inspected by the FDA in 2014 and
received two negative observations.48
Similar presentations about compliance matters were given to the Board and
Audit Committee at regular intervals during the remainder of 2015 and 2016.49
Those presentations about “FDA and Quality Matters” would mention, among other
things, FDA inspections and third-party audits at various sites, the results of those
inspections, responses to prior observations, and plans for remediation.50 The Board
46 Id. ¶ 129.
47 Id.
48 Id. ¶ 131.
49 The Complaint discusses Board and Audit Committee meetings and presentations in 2015 and 2016 on: July 17, 2015; September 25, 2015; December 11, 2015; February 23, 2016; May 3, 2016; July 15, 2016; August 5, 2016 (Audit Committee); September 23, 2016; October 24, 2016 (Audit Committee); and December 16, 2016. See id. ¶¶ 127–88. 50 See id. ¶¶ 126–94.
would be told about issues at Zimmer facilities spanning the globe from Jinhua,
China to Montreal, Canada.51
In October and November 2015, the FDA conducted a scheduled inspection
of Zimmer’s West Campus facility in Warsaw, Indiana and issued a Form 483 listing
10 negative observations, nine of which were repeat observations from prior FDA
inspections.52 Around the same time, the FDA was also inspecting the Company’s
Ponce, Puerto Rico facility.53 That inspection resulted in four negative observations,
including three repeat observations.54 The Zimmer Board learned about the West
Campus Form 483, the Ponce inspection, and other FDA inspections of Zimmer
facilities during its December 11, 2015 meeting.55
By the time of the February Offering, the Board was aware that certain
facilities were having “extensive FDA compliance problems”—including that West
Campus and Ponce had received Form 483s and that Zimmer’s Jinhua, China facility
had received an FDA Warning Letter.56 The plaintiffs also allege that the Board
51 See id. ¶ 11.
52 Id. ¶¶ 106–07.
53 Id. ¶ 109.
54 Id.
55 Id. ¶¶ 143–44. On December 21, 2015, Zimmer responded to the West Campus Form 483, noting that it was working to “address systemic issues.” Id. ¶ 108. On February 12, 2016, Zimmer told the FDA that its remediation efforts at the West Campus would not be complete until June of 2017. Id. ¶ 110. 56 Id. ¶ 268.
knew that Zimmer planned to conduct internal audits into FDA-readiness at various
sites.57
D. Zimmer Conducts Internal Audits and the Board Receives Regular Updates on Compliance.
Various compliance matters at Zimmer facilities were identified for the Board
after the February Offering. A Board presentation given at a February 23, 2016
meeting listed eight separate FDA investigations that identified one or more negative
observations, including seven negative observations at Zimmer’s Montreal site.58 At
that same meeting, the Board was told about the Company’s plans to audit Zimmer’s
network of manufacturing facilities, including the North Campus.59
The results of those internal audits were issued in March, April, and June 2016
reports, including observations from Zimmer’s North Campus facility—where “key
brands” providing the Company with some of its “best competitive opportunities”
were made—among others.60 Zimmer’s March 31, 2016 internal audit report titled
“Corporate Complaints Process Audit” detailed six major and two minor
57 Id.; see also Barillare Decl. Ex. 11 (Sept. 25, 2015 Zimmer Board meeting minutes and presentation slides) (Dkt. 75). 58 Compl. ¶¶ 111 (quoting Barillare Decl. Ex. 12 (Feb. 23, 2016 Zimmer Board meeting minutes and presentation slides)), 154. 59 Id. ¶¶ 153–55; see Barillare Decl. Ex 12.
60 Compl. ¶ 12.
observations at the North Campus facility.61 The April 13, 2016 internal audit report
titled “Corporate Design Controls Audit” listed four critical and 15 major
observations at the North Campus.62 And the June 7, 2016 internal audit report titled
“Corporate General QMS Audit” described 15 major and five minor observations at
the North Campus.63
The plaintiffs assert that the “audit results were provided to the Board no later
than May 3, 2016 (with the third report then in draft).”64 But the plaintiffs do not
allege that the Board received a copy of the audit reports or a description of the
compliance issues they addressed. The Board was given the following information
in a May 3, 2016 Board presentation slide that allegedly corresponds to the three
North Campus internal audits:65
61 Id. ¶ 124; see Barillare Decl. Ex. 17 (Dec. 16, 2016 Zimmer Board meeting minutes and presentation slides) at 2. 62 Compl. ¶ 124.
63 Id.
64 Id. ¶ 13; see also id. ¶ 147 & n.15.
65 Id. ¶ 159 & n.18; see Barillare Decl. Ex. 13 (May 3, 2016 Zimmer Board meeting minutes and presentation slides).
Zimmer Biomet Location Audit Entity Status Result Establishment Date EtQ Complaints N/A Dec ‘15 – ZBQC Reports 13 – Major Enterprise Audit – Mar ‘16 issued 4 – Minor Multiple Sites 3/31/16 Biomet Warsaw Warsaw, March 14- PAREXEL Report 4 – Critical North (Design & IN 18 K&S issued 15 – Major Package) 4/13/16 Corporate Audit N/A Mar 2 DLSS Report in TBD Process draft
The slide also listed similar information for 11 other audits, with varying degrees of
results.66 In total, the audits listed on the slide noted seven critical and 62 major
observations.67 The May 3, 2016 Board meeting was the last meeting before the
June Offering.68
The Board next met on July 15, 2016. Once again, the Board received a
presentation on “FDA and Quality Matters” at various Zimmer facilities.69 The
directors were updated on ongoing compliance remediation efforts at Zimmer sites.70
They were informed, among other things, that certain remediation efforts at the
66 See Compl. ¶ 159; Barillare Decl. Ex. 13.
67 Compl. ¶¶ 159, 161.
68 On May 27, 2016, the FDA issued a Warning Letter to Zimmer’s Montreal facility. Id. ¶ 165. The plaintiffs do not allege that the Board was informed of that Warning Letter before the June Offering. 69 Id. For example, the Board learned that a recent FDA inspection at Zimmer’s Dover, Ohio facility had resulted in four negative observations. Id. 70 Id. ¶ 167.
North Campus would not be complete until 201871 and that several observations
from the West Campus Form 483 remained open.72 The July 15, 2016 meeting was
the last time the full Board met before the August Offering, though the Audit
Committee met on August 5, 2016.73
E. Zimmer Lowers Guidance After the 2016 North Campus FDA Inspection and Product Ship Hold.
The FDA inspection at the core of the plaintiffs’ Complaint occurred on
September 12, 2016—more than a month after the August Offering.74 That day, the
FDA commenced an unannounced for cause inspection at Zimmer’s North Campus
facility.75 The Board was told about the in-progress inspection during an “FDA
Update” at a regularly scheduled meeting on September 23, 2016.76
Between the start of the inspection and September 28, 2016, the FDA
identified significant issues with Zimmer’s quality systems at the North Campus.77
The inspection led to immediate disruptions to the North Campus’s operations and
71 Id.
72 Id. ¶ 169.
73 The Audit Committee met to discuss the KKR Fund’s and TPG Funds’ planned sales of Zimmer stock in the August Offering. Id. ¶ 172. 74 Id. ¶ 113.
75 Id.
76 Id. ¶ 175; Barillare Decl. Ex. 15 (Sept. 23, 2016 Zimmer Board meeting minutes and presentation slides). 77 See Compl. ¶ 114.
the shipment of key products.78 As a result, on September 29, 2016, Zimmer
implemented a blanket product ship hold “to stop shipments of all final product
cleaned, sterile packed, and sterilized at the Warsaw North Campus.”79 The third
quarter ended the next day. A month’s worth of supply shortages came after the ship
hold.80
In the weeks that followed, the Company implemented other holds on
materials and finished products at the North Campus.81 On October 21, 2016, the
blanket product ship hold began to be released in stages based on remediation
efforts.82
On October 24, 2016, the Audit Committee—along with Zimmer’s officers,
its counsel, and its external auditor—met to review the Company’s draft earnings
release for the third quarter of 2016 and were given an “update on the ongoing FDA
inspection” of the North Campus.83 After discussion, the Audit Committee members
“expressed no objections” to the contents of the draft release.84
78 Id.
79 Id. ¶ 115 (quoting Barillare Decl. Ex. 17 at 4).
80 Id.
81 Id.
82 Id.
83 Id. ¶ 181 (quoting Barillare Decl. Ex. 18 (Oct. 24, 2016 Zimmer Audit Committee meeting minutes) at 2). 84 Id. (quoting Barillare Decl. Ex. 18 at 2).
Zimmer released its third quarter 2016 results on October 31, 2016.85 It
reported organic sales growth of 1.6%, which was below expectations. 86 The
Company also reduced its revenue guidance for the fourth quarter of 2016.87 The
results caused Zimmer’s stock price to drop nearly 14%, from a high of $122.55 the
previous trading day to a closing price of $105.40 on October 31. 88 The North
Campus FDA inspection and the related product ship holds were not mentioned in
the earnings release or during Dvorak’s earnings call with investors.89
On November 8, 2016, Zimmer filed its Form 10-Q for the period ending
October 31, 2016.90 The Company reported that its below guidance revenue results
were attributable in part to “some temporary disruption in product supply . . . related
to several factors, including implementation of operational process enhancements
that have resulted in various shipment delays, and manufacturing forecasting
constraints related to continued integration of our supply chain . . . .”91 The Form
10-Q did not explicitly mention the FDA inspection at the North Campus or the
related product ship holds.
85 Id. ¶ 217.
86 Id.
87 Id.
88 Id.
89 See id. ¶¶ 218–19.
90 Id. ¶ 221.
91 Id. (alterations in original).
F. The North Campus Inspection and Product Ship Holds Are Reported.
The same day that Zimmer filed its third quarter 2016 Form 10-Q, an analyst
at Northcoast Research reported on the FDA’s inspection of the North Campus and
the related product ship holds.92 Northcoast reasoned that the “product supply
issues” Zimmer had announced were due “at least [in] part” to the FDA inspection
and shut down of certain product lines.93 Zimmer disclosed, in response to
Northcoast’s report, that it was “in the process of deploying new demand planning
and production planning tools” and that “enhance[ments]” to “harmonize[ ] and
optimize[ ]” its processes “led to certain product shipment delays, including product
manufactured at the [North Campus].”94 Zimmer also said that it expected “to return
to full shipping capacity with the impacted products over the next few weeks.”95
Zimmer’s stock price continued to decline, reaching a low of $97.99 on
November 14, 2016.96
92 Id. ¶ 220.
93 Id.
94 Id. ¶ 222.
95 Id.
96 Id. ¶ 223.
G. The FDA Issues a Form 483 Related to the North Campus Inspection.
On November 22, 2016, the FDA issued a 57-page Form 483 based on the
North Campus inspection.97 The FDA identified 14 negative observations, two of
which were repeat observations from the North Campus’s 2014 FDA inspection.98
Analysts obtained the Form 483 through Freedom of Information Act requests on or
around December 14, 2016.99 Morningstar Research reported it was “skeptical” that
the FOIA requests would uncover any information and noted that they had “seen
other medical device firms take a more proactive stance in these situations to
reassure investors that management was working decisively to resolve the FDA’s
issues.”100 A consultant for Wells Fargo & Company commented that the 57-page
Form 483 was “the longest one he remembers seeing” and that it was “quite unusual”
for a Form 483 “to be so thorough in documenting a company’s perceived
shortcomings.”101
On December 14, 2016, Zimmer responded to the Morningstar Research
report, noting that it “ha[d] developed and [wa]s executing a remediation plan to
97 Id. ¶ 116.
98 Id. ¶¶ 116–17.
99 Id. ¶¶ 228–29.
100 Id. ¶ 229.
101 Id. ¶ 230.
fully address the issues cited by the FDA.”102 Zimmer also said that it was “taking
the necessary steps to address certain regulatory compliance gaps” at the North
Campus site.103 Zimmer further explained that “the anticipated full impact of all of
the above-described matters was included in [its] sales and earnings guidance update
issued on October 31, 2016.”104
The Board met two days later for a regularly scheduled meeting on December
16, 2016.105 As usual, the Board was given a presentation called “FDA and Quality
Matters.”106 The directors were updated on the status of Zimmer’s internal audit
remediation efforts, including a site remediation plan for the North Campus.107
Between December 21, 2016 and April 25, 2017, Zimmer sent four written
responses to the FDA about the North Campus.108 In total, these responses to the
FDA consisted of more than 22,000 pages.109 The responses outlined the Company’s
internal audits and actions to address “systemic issues.”110 The Board continued to
102 Id. ¶ 231.
103 Id.
104 Id.
105 Id. ¶ 184.
106 Id.; Barillare Decl. Ex. 16 (Dec. 16, 2016 Zimmer Board meeting minutes and presentation slides). 107 Compl. ¶ 185; Barillare Decl. Ex. 16.
108 Compl. ¶ 190.
109 Id.
110 Id.; see Barillare Decl. Ex. 17 at 2.
receive regular updates on the North Campus inspection and Zimmer’s response
throughout 2017 and 2018.111
H. Litigation Ensues
Lawsuits began within a month of Zimmer reducing its guidance for the third
quarter of 2016. On December 2, 2016, a securities class action was filed in the
United District Court for the Northern District of Indiana against Zimmer and certain
of its directors and officers (the “Securities Class Action”).112 The PE Funds other
than the Blackstone Fund were later named as defendants in a second amended
complaint filed in October 2017.113 On September 26, 2018, the district court in
Indiana denied Zimmer and the individual defendants’ motion to dismiss the
Securities Class Action,114 but granted the PE Funds’ motions to dismiss.115 At the
time the Complaint in this action was filed, the parties to the Securities Class Action
had announced a proposed settlement of $50 million.116
111 See Compl. ¶¶ 189–94.
112 Id. ¶ 279.
113 See Second Am. Class Action Compl. for Violations of the Fed. Sec. Laws, Shah v. Zimmer Biomet Hldgs., Inc., 348 F. Supp. 3d 821 (N.D. Ind. 2018) (No. 3:16-cv-00815- PPS-MGG), 2017 WL 5494812 (Dkt. 60). 114 See Compl. ¶¶ 283–86; Shah v. Zimmer Biomet Hldgs., Inc., 348 F. Supp. 3d 821, 851 (N.D. Ind. 2018). 115 Shah, 348 F. Supp. 3d at 851.
116 Compl. ¶ 287.
Litigation in this court began on June 14, 2019 with the filing of two separate
complaints that relied upon books and records Zimmer had produced under 8 Del.
C. § 220.117 Those actions were consolidated on September 4, 2019.118 The
plaintiffs filed the operative Complaint on June 3, 2020.119
The Complaint advances six counts derivatively on behalf of Zimmer: breach
of fiduciary duty against the individual defendants in Count I; insider trading against
Michelson and Rhodes under Brophy v. Cities Service Company in Count II;120
aiding and abetting against the PE Funds in Counts III and IV; unjust enrichment
against the individual defendants and the PE Funds in Count V; and breach of
contract against the PE Funds in Count VI. On September 14, 2020, each of the
defendants moved to dismiss the Complaint.121
II. LEGAL ANALYSIS
The defendants have moved to dismiss the Complaint under Court of
Chancery Rule 23.1 for failure to make a demand on the Board. All defendants
except Zimmer have also moved to dismiss the Complaint under Court of Chancery
117 See Dkt. 10; Compl. at 3.
118 Dkt. 10.
119 Dkt. 47.
120 70 A.2d 5 (Del. Ch. 1949).
121 See Dkts. 67, 69, 72, 76. After briefing, the court heard oral argument on June 15, 2021. Dkt. 104.
Rule 12(b)(6) for failure to state a claim on which relief can be granted. The demand
requirement of Rule 23.1 presents a threshold issue as to all counts in the Complaint.
A. The Legal Standard for Demand Excusal
“The decision whether to initiate or pursue a lawsuit on behalf of the
corporation is generally within the power and responsibility of the board of
directors.”122 A stockholder plaintiff can only pursue claims belonging to the
corporation if (1) the corporation’s directors wrongfully refused a demand to
authorize the corporation to bring the suit or (2) a demand would have been futile
because the directors were incapable of impartially considering the demand.123
Because the plaintiffs did not make a demand on Zimmer’s Board, the Complaint
must plead particularized factual allegations establishing that demand was
excused.124 All of the parties agree that the standard for assessing demand excusal
in this case is set forth in Rales v. Blasband.125 The court applies Rales when “the
board that would be considering the demand did not make a business decision which
is being challenged in the derivative suit,” such as “where directors are sued
derivatively because they have failed to do something.”126
122 In re Citigroup Inc. S’holder Deriv. Litig., 964 A.2d 106, 120 (Del. Ch. 2009) (citing 8 Del. C. § 141(a)). 123 See Rales v. Blasband, 634 A.2d 927, 932 (Del. 1993).
124 Ct. Ch. R. 23.1; see, e.g., Guttman v. Huang, 823 A.2d 492, 499 (Del. Ch. 2003).
125 634 A.2d 927 (Del. 1993).
126 Id. at 933–34 & n.9.
Under Rales, demand is excused if the allegations in a complaint “create a
reasonable doubt that, as of the time the complaint is filed, the board of directors
could have properly exercised its independent and disinterested business judgment
in responding to a demand.”127 To that end, “[a] director cannot exercise . . .
independent and disinterested business judgment where [the] director is ‘either
interested in the alleged wrongdoing or not independent of someone who is.’”128 If
“the directors face a ‘substantial likelihood’ of personal liability, their ability to
consider a demand impartially is compromised under Rales, excusing demand.”129
While engaging in this analysis, I confine myself to the well-pleaded
allegations of the Complaint, the documents incorporated into the Complaint by
reference, and facts subject to judicial notice.130 All reasonable inferences from the
allegations in the Complaint are drawn in favor of the plaintiffs.131 “Rule 23.1 is not
satisfied by conclusory statements or mere notice pleading.”132 Instead, “[w]hat the
127 Id. at 934.
128 Teamsters Local 443 Health Servs. & Ins. Plan v. Chou, 2020 WL 5028065, at *15 (Del. Ch. Aug. 24, 2020) (quoting Hughes v. Hu, 2020 WL 1987029, at *12 (Del. Ch. Apr. 27, 2020)). 129 Guttman, 823 A.2d at 501.
130 See, e.g., White v. Panic, 783 A.2d 543, 546–47 (Del. 2001); see also In re Gen. Motors (Hughes) S’holder Litig., 897 A.2d 162, 170 (Del. 2006). 131 Brehm v. Eisner, 746 A.2d 244, 255 (Del. 2000).
132 Id. at 254.
pleader must set forth are particularized factual statements that are essential to the
claim.”133
B. The Demand Excusal Analysis in This Case The court “counts heads” of the members of a board to determine whether a
majority of its members are disinterested and independent for demand futility
purposes.134 The Board in place when this litigation was filed had 11 members:
Higgins and Michelson; Director Defendants Begley, Bernard, Boudreux, Farrell,
Glasscock, Hagemann; and non-parties Jafry, Hilado, and Hanson (together, the
“Demand Board”).135 The plaintiffs concede that Jafry, Hilado, and Hanson do not
face a substantial likelihood of liability.136 And they only allege that three members
of the Demand Board—Michelson, Higgins, and Hanson (as Zimmer’s CEO)—lack
independence or received some benefit from the PE Funds’ stock sales.137 Even if
the plaintiffs could sufficiently demonstrate that those three directors lacked
independence,138 they must also impugn the disinterestedness of at least three others
133 Id.
134 See In re EZCORP Inc. Consulting Agreement Deriv. Litig., 2016 WL 301245, at *34 (Del. Ch. Jan. 25, 2016). 135 Compl. ¶ 294.
136 See id. ¶ 29.
137 Id. ¶¶ 294 n.29, 311–12, 326.
138 The plaintiffs contend only that Michelson was personally interested in the challenged stock offerings. See id. ¶¶ 311–12. Little is said about the interests of Higgins except that he was employed by Blackstone’s healthcare group Blackstone Healthcare Partners as a “Consultant.” Id. ¶¶ 41, 51. The plaintiff’s only allegation about Hanson is that he “is not
(i.e., three of Begley, Bernard, Boudreux, Farrell, Glasscock, and Hagemann) to
show that a majority of the Demand Board was disabled from considering a
demand.139 The plaintiffs attempt to make that showing by arguing that the Director
Defendants all face a substantial likelihood of personal liability.
“To establish a substantial likelihood of liability at the pleading stage, a
plaintiff must ‘make a threshold showing, through the allegation of particularized
facts, that their claims have some merit.’”140 Because Zimmer’s certificate of
incorporation contains an exculpation provision under 8 Del. C. § 102(b)(7),141 the
plaintiffs must plead with particularity facts that support a meritorious claim for
breach of the duty of loyalty.142 The Complaint primarily focuses on whether
material non-public information about Zimmer’s FDA compliance challenges
independent from interested directors due to his principal occupation as Zimmer’s CEO.” Id. ¶ 294 n.29. The defendants declined to brief whether Higgins, Michelson, and Hanson could impartially consider a demand. See Zimmer Defs.’ Opening Br. at 26 (saying the court “need not consider” the plaintiffs’ allegations about the independence of those three directors). I need not reach the issue of whether Michelson, Higgins, or Hanson could impartially consider a demand because—even if they could not—the plaintiffs cannot establish demand futility. 139 See Pls.’ Answering Br. 7 n.2 (Dkt. 85).
140 In re TrueCar, Inc. S’holder Deriv. Litig., 2020 WL 5816761, at *12 (Del. Ch. Sept. 30, 2020) (quoting Rales, 634 A.2d at 934).
Barillare Decl. Ex. 9 (Zimmer’s Restated Certificate of Incorporation dated June 24, 141
2015) § 10.01. 142 TrueCar, 2020 WL 5816761, at *12; In re Goldman Sachs Gp., Inc. S’holder Litig., 2011 WL 4826104, at *12 (Del. Ch. Oct. 12, 2011).
played a role in the PE Funds’ sales of over $3.3 billion in Zimmer stock in 2016.143
The problem for the plaintiffs is that they failed to plead non-conclusory facts
suggesting that a super-majority of directors without ties to the PE Funds knowingly
facilitated insider trading. Perhaps recognizing that hurdle, they also assert that the
eight members of the Demand Board named as defendants in this action face a
substantial likelihood of liability for approving false and misleading disclosures, for
breaching their duty of oversight, and based on the Securities Class Action. I will
address each argument in turn below.
The outcome of my analysis is that none of the six Director Defendants face
a substantial likelihood of liability in this action or the Securities Class Action. The
plaintiffs get closest with a disclosure claim against the four Audit Committee
members (Begley, Boudreaux, Glasscock, and Hagemann) but fall short of pleading
a breach of the duty of loyalty. The result is that at least eight of the 11 Demand
Board members are independent, had no ties to the PE Funds or disabling interests
from the stock sales, and did not face a risk of liability for a non-exculpated claim.
1. The Disclosure Claim
Although the crux of the wrongdoing alleged in the Complaint is insider
trading, the plaintiffs’ demand futility arguments mostly focus on disclosures. The
Complaint challenges numerous “SEC filings, press releases, conference calls, and
143 See, e.g., Compl. ¶ 1.
presentations to the public” Zimmer made during the relevant period,144 including
the Registration Statement and prospectuses related to the February, June, and
August Offerings.145 The gist of the plaintiffs’ disclosure argument is that Zimmer
was publicizing the “purported successful integration [of Legacy Zimmer and
Legacy Biomet] and the Company’s growing organic growth rate” at a time that
Zimmer was privately facing quality and regulatory deficiencies.146 In particular,
they assert that all of Zimmer’s public disclosures in 2016 were false and misleading
because they “touted the purported ongoing success of the integration of [Legacy]
Zimmer and [Legacy] Biomet,” but “failed to disclose known systemic quality
system and quality control problems,” “the Company’s FDA regulatory
deficiencies,” and “the massive remediation efforts that were necessary to bring
Zimmer into compliance with FDA regulations and that would adversely impact
production and distribution of key products.”147 The plaintiffs claim generally that
Zimmer omitted material information from its public statements rather than
challenge any specific statements by Zimmer as false or misleading.148
144 Id. ¶ 196; see id. ¶¶ 215, 221, 263, 265–66, 306, 333.
145 See id. ¶¶ 215, 257, 260, 306, 315, 317, 333.
146 Id. ¶ 195.
147 Id. ¶¶ 211, 266.
148 See Citigroup, 964 A.2d at 133 (“[T]he disclosure allegations in the complaint do not meet the stringent standard of factual particularity required under Rule 23.1. They fail to allege with particularity which disclosures were misleading, when the Company was
“Whenever directors communicate publicly or directly with shareholders
about the corporation’s affairs, with or without a request for shareholder action,
directors have a fiduciary duty to shareholders to exercise due care, good faith and
loyalty.”149 The duty of disclosure “is not an independent duty, but derives from the
duties of care and loyalty.”150 The contours of that duty and what it requires of
fiduciaries are context specific. Where (like here) the disclosures at issue do not
concern a request for stockholder action, Malone v. Brincat requires that a plaintiff
demonstrate scienter—i.e., that the directors “deliberately misinform[ed]
shareholders about the business of the corporation, either directly or by a public
statement.”151 Because Zimmer’s certificate of incorporation includes a Section
102(b)(7) provision, the plaintiffs “must plead particularized factual allegations that
‘support the inference that the disclosure violation was made in bad faith, knowingly
or intentionally’”152 to establish demand futility.
A determination of “whether the alleged misleading statements or omissions
were made with knowledge or in bad faith requires an analysis of the state of mind
obligated to make disclosures, what specifically the Company was obligated to disclose, and how the Company failed to do so.”). 149 Malone v. Brincat, 722 A.2d 5, 10 (Del. 1998).
150 Pfeffer v. Redstone, 965 A.2d 676, 684 (Del. 2009) (citation and internal quotation marks omitted). 151 Malone, 722 A.2d at 14.
152 Citigroup, 964 A.2d at 132 (quoting O’Reilly v. Transworld Healthcare, Inc., 745 A.2d 902, 915 (Del. Ch. 1999)).
of the individual director defendants.”153 It is difficult to know one’s state of mind
at the pleadings stage, particularly for independent directors that lack any obvious
motivations to act disloyally.154 Delaware courts may infer scienter for Malone
claims where certain types of specific factual allegations are made. A plaintiff must
plead with particularly that directors “had knowledge that any disclosures or
omissions were false or misleading or . . . acted in bad faith in not adequately
informing themselves.”155 A plaintiff also must allege “sufficient board involvement
in the preparation of the disclosures”156 to “connect the board to the challenged
statements.’”157 Despite having access to the relevant Board minutes and materials,
however, the plaintiffs cannot link what the directors learned about continuing FDA
compliance challenges with any materially misleading statements they were
responsible for making.
153 Id. at 134; see also Ryan v. Armstrong, 2017 WL 2062902, at *5 (Del. Ch. May 15, 2017) (discussing how directors’ “motives, background, or relationships” factor into the demand futility analysis), aff’d, 176 A.3d 1274 (Del. 2017) (TABLE). 154 See In re GoPro, Inc., 2020 WL 2036602, at *11 (Del. Ch. Apr. 28, 2020) (observing a lack of pleaded facts allowing for an inference that a majority of the board was beholden to defendants who sold shares “such that [the directors] would be motivated to facilitate or cover up illegal insider trading”). 155 Citigroup, 964 A.2d at 134.
156 Id.; see also id. at 133 n.91 (explaining that a plaintiff must “sufficiently allege facts showing that the director defendants were involved in preparing (or were otherwise responsible for) the alleged misleading disclosures”). 157 TrueCar, 2020 WL 5816761, at *13 (internal quotation marks omitted); see also In re Dow Chem. Co. Deriv. Litig., 2010 WL 66769, at *11 (Del. Ch. Jan. 11, 2010).
The Complaint alleges that the Board knew about “undisclosed, serious, and
‘systemic’ quality control issues across many of its manufacturing facilities
throughout 2015 and 2016.”158 According to the plaintiffs, the eventual temporary
shutdown at the North Campus was “easily foreseeable” because of Zimmer’s
regulatory compliance issues.159 But, the plaintiffs say, despite “actual knowledge
of” Zimmer’s FDA compliance struggles, the Director Defendants “knowingly
failed” to disclose those risks and violations to the public.160
The operative inquiry for the court is determining when a majority of the
Demand Board both learned about the potentially problematic event “and understood
its significance to [the company’s] financial performance.”161 This court’s decision
in TrueCar is instructive. There, the plaintiffs alleged that the board learned of a
website redesign that had a materially negative effect on the company’s financial
performance but failed to disclose it.162 The court found that because the board
materials did not reflect any expected financial harm from the redesign, the plaintiffs
“failed to allege with particularity facts sufficient to support a reasonable inference
158 Compl. ¶ 7; see also Pls.’ Answering Br. 35.
159 Compl. ¶ 112.
160 Pls.’ Answering Br. 33, 35.
161 TrueCar, 2020 WL 5816761, at *14.
162 Id.
of scienter, i.e., that the directors . . . knew before they signed or approved” the
challenged disclosure that the company’s business would subsequently “suffer.”163
Here, the question I must consider for purposes of that analysis is when the
Board understood both that the North Campus was in severe violation of FDA
regulations and that the lack of compliance would have a materially negative effect
on Zimmer’s financial performance. The plaintiffs argue that the Board’s
knowledge derives from the three internal audit reports, the FDA’s September 12,
2016 inspection of the North Campus, and the resulting blanket product ship hold.164
To examine the directors’ knowledge, the court will consider the plaintiffs’
allegations chronologically for three time periods: (i) before May 3, 2016; (ii) from
May 3, 2016, when the Board was informed about results from the internal audit
reports, to September 12, 2016; and (iii) from September 12, 2016, when the FDA’s
for cause inspection of the North Campus began, forward.
a. Before the May 3, 2016 Board Meeting
The plaintiffs allege that the Board “already kn[ew]” about “significant
violations” at the North Campus before the May 3, 2016 Board meeting where
internal audit results were first discussed.165 The Complaint explains that the Board
163 Id. at *15.
164 See Compl. ¶¶ 18–22, 113–19.
165 Id. ¶ 18.
routinely received presentations about the Company’s regulatory compliance
performance during regularly scheduled meetings after the merger closed in June
2015. But the presentations the Board received at meetings between July 17, 2015
(the first Board meeting post-merger) and May 3, 2016 contain only limited and
unremarkable mentions of the North Campus.166 None of the references to
“systemic” issues or negative observations at other Zimmer facilities are alleged to
be related to what eventually transpired at the North Campus.
Each of the Board presentations during this time period follow a similar
pattern: they list the results of FDA inspections at various Zimmer facilities, certain
negative observations from those inspections, and plans for remediation. For
example, on July 17, 2015, the Board was told that the North Campus (among other
Legacy Biomet facilities) had been inspected in 2014, receiving two negative
observations,167 and that the North Campus was due for its biennial FDA inspection
in 2016.168 The Board was also told that outside consulting firm Parexel had
performed a mock inspection of the North Campus that identified 11 major and seven
minor observations leading Zimmer to open 10 “action records” to address those
observations.169 For the next three Board presentations at meetings held on
166 See id. ¶¶ 127–57 (discussing Board presentations from this time period).
167 Id. ¶ 131.
168 Id. ¶ 268.
169 Id. ¶ 131.
September 25, 2015, December 11, 2015, and February 23, 2016,170 the only
mention of North Campus that the plaintiffs identify is that the Company “planned
to audit the North Campus facility in the second quarter of 2016” as part of Zimmer’s
2016 corporate audit plan.171
These Board presentations tell a story of Zimmer’s ongoing efforts to ferret
out compliance issues and fix them but provide no indication that the North Campus
was a “ticking time bomb.”172 That is, the portions of the presentations that the
plaintiffs highlight are insufficient to demonstrate with particularity that the Director
Defendants present at these meetings knew that serious compliance issues were
looming at the North Campus that would ripen into negative financial
consequences.173 This pleading deficiency is enough to eliminate an inference of
bad faith misconduct, especially since there is no allegation that the Director
Defendants failed to adequately inform themselves. But there are several other
issues that further undermine any finding that the Director Defendants face a
substantial threat of personal liability for a non-exculpated disclosure claim.
170 See id. ¶¶ 135–57.
171 Id. ¶ 147.
172 Id. ¶ 270.
173 E.g., TrueCar, 2020 WL 5816761, at *14-15. Eight Demand Board members are alleged to have attended the July, September, and December 2015 Board meetings. Compl. ¶¶ 133, 140, 151. Six Demand Board members are alleged to have attended the February 2016 Board meeting. Id. ¶ 156.
First, the “plaintiffs fail to allege with sufficient specificity the actual
misstatements or omissions that constituted a violation of the board’s duty
of disclosure.”174 It is entirely unclear from their scattered allegations what precisely
the plaintiffs believe was material information that the Board should have disclosed
during this period. Plainly, every negative observation from all of Zimmer’s
facilities would not have been important information to investors.175
The closest the plaintiffs get to the required specificity is an allegation that the
Director Defendants “allow[ed]” Zimmer to “issue materially false and misleading
statements and omissions about the purported successful integration and the
Company’s growing organic growth rate.”176 There are no particularized facts in the
Complaint, however, that would support an inference that Legacy Zimmer and
Legacy Biomet were not integrating as planned. As to Zimmer’s organic growth
rate, Zimmer reported a better-than-expected growth rate of 1.2% for the first quarter
174 See Citigroup, 964 A.2d at 133 (finding that “the disclosure allegations in the complaint do not meet the stringent standard of factual particularity required under Rule 23.1”). 175 In fact, disclosing every negative compliance violation would have cut against the goal of highlighting material information for stockholders. See Abrons v. Maree, 911 A.2d 805, 813 (Del. Ch. 2006) (“Delaware courts must ‘guard against the fallacy that increasingly detailed disclosure is always material and beneficial disclosure.’” (quoting Zirn v. VLI Corp., 1995 WL 362616, at *4 (Del. Ch. June 12, 1995) (Chancellor Allen noting that “[i]n some instances, the opposite will be true”), aff’d, 681 A.2d 1050 (Del.1996)); see also In re Rouse Properties, Inc., 2018 WL 1226015, at *24 (Del. Ch. Mar. 9, 2018) (noting that disclosure of “insignificant detail[s]” could “dilute the value and purpose of public corporate disclosures”). 176 Compl. ¶ 195.
of 2016 and raised its revenue guidance for the remainder of the year.177 There is
nothing inherently misleading about the disclosures on these topics.
Moreover, the Complaint lacks allegations demonstrating actual Board
involvement in or responsibility for disclosures. Several of the statements that the
plaintiffs appear to challenge during this time period were made by Zimmer officers
during earnings calls or at conferences where the Board is not alleged to have played
any role.178 The plaintiffs’ arguments about Zimmer’s public filings fare no better.
The disclosures filed with the Securities and Exchange Commission that the
plaintiffs challenge as “false and misleading” during this time period are: (1) the
2015 Form 10-K (filed with the SEC on February 29, 2016); (2) the first quarter
2016 Form 10-Q (filed with the SEC on May 10, 2016), (3) the Registration
Statement (filed with the SEC on February 4, 2016); and (4) the prospectus
supplements for the February Offering (filed with the SEC on February 5, 2016 and
February 8, 2016).179
The only mentions in the Complaint of Board involvement in the 2015 Form
10-K, the Registration Statement, and the prospectus supplements are the types of
allegations that this court has repeatedly found inadequate for purposes of Rule 23.1.
177 Id. ¶ 202.
178 See id. ¶¶ 198–201.
179 See id. ¶¶ 215, 260.
A statement that the documents were signed by the Director Defendants,180 or that
they “approved” the disclosures and “caused” or “consented to” their filing,181 is
not—without more—a particularized allegation of fact.182 There are also no specific
180 See id. ¶¶ 35–45, 306, 314; see also Pls.’ Answering Br. 21 (asserting that “[e]ight directors reviewed, signed, approved, and issued the Registration Statement and Prospectuses used in the three offerings”). 181 Compl. ¶¶ 260, 263, 265, 328, 338.
182 Ellis v. Gonzalez, 2018 WL 3360816, at *10 (Del. Ch. July 10, 2018), aff’d, 205 A.3d 821 (Del. 2019); Citigroup, 964 A.2d at 133 n.88 (“Pleading that the director defendants ‘caused’ or ‘caused or allowed’ the Company to issue certain statements is not sufficient particularized pleading to excuse demand under Rule 23.1.”); see also Brehm, 746 A.2d at 254; In re China Auto. Sys. Inc. Deriv. Litig., 2013 WL 4672059, at *8 (Del. Ch. Aug. 30, 2013) (finding the allegation “that all five directors attested to the misleading financial statements by signing one of the SEC filings at issue” insufficient to excuse demand (internal citation omitted)).
The Court of Chancery has found allegations that a defendant signed an allegedly false or misleading disclosure sufficient to state a claim for relief under the lower pleading standard of Rule 12(b)(6). See In re Hansen Med., Inc. S’holders Litig., 2018 WL 3025525, at *11 (Del. Ch. June 18, 2018). That is not the case where the heightened pleading standard of Rule 23.1 applies. In addition, having reviewed the prospectuses issued in connection with the February, June, and August Offerings, none appear to bear the signature of any Director Defendant. See Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (Feb. 5, 2016); Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (Feb. 8, 2016); Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (June 13, 2016); Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (June 15, 2016); Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (Aug. 9, 2016); Zimmer Biomet Hldgs., Inc., Prospectus Suppl. (Form 424B7) (Aug. 11, 2016); see also Gen. Motors (Hughes), 897 A.2d at 170 (permitting the court to take judicial notice of “hearsay in SEC filings” that is not subject to reasonable dispute).
The plaintiffs also note that “[t]o the extent the Director Defendants seek to limit their liability solely to public filings that they ‘signed,’ that argument would have little effect here, where the Registration Statement and the Offering Documents incorporated by reference other public filings at issue in this case such as the 10-K, including, specifically, the risks and uncertainties disclosed in each of those public filings.” Pls.’ Answering Br. 41 n.12. The plaintiffs cite no case to support this argument, and the court is aware of none.
allegations in the Complaint about the first quarter 2016 Form 10-Q. The plaintiffs
only make general assertions about the role of the Audit Committee in reviewing
quarterly financial statements and overseeing certain internal controls disclosures,183
which are insufficient to demonstrate the Audit Committee’s actual involvement in
the statements in (or omissions from) the Form 10-Q.184 The lack of well-pleaded
allegations about the Director Defendants’ involvement in the disclosures
“independently preclude[s] a finding of demand futility.”185
b. Between the May 3, 2016 Board Meeting and September 12, 2016 Inspection
The plaintiffs contend that the Board’s knowledge of serious problems
changed after May 3, 2016. According to the Complaint, the Board learned “no later
than May 3, 2016” that Zimmer’s “most important” facility—the North Campus—
“was in a terrible state of FDA compliance” and a “disaster waiting to happen.”186
183 Compl. ¶ 79. The Complaint describes the Audit Committee’s responsibilities as including “review[ing] and discuss[ing] with management and the independent auditor the quarterly financial statements prior to their public release.” Id. 184 See Wood v. Baum, 953 A.2d 136, 142 (Del. 2008) (“Plaintiff also asserts that membership on the Audit Committee is a sufficient basis to infer the requisite scienter. That assertion is contrary to well-settled Delaware law.”); Ellis, 2018 WL 3360816, at *11 (finding argument that audit committee members could not impartially consider a demand given their “oversight responsibility” unpersuasive because it “runs up against the well- settled rule that mere membership on a board committee is insufficient to support a reasonable inference of disloyal conduct”). Further, these allegations are not determinative as to the court’s demand futility analysis because the Audit Committee members constitute a minority of the Demand Board. 185 Ellis, 2018 WL 3360816, at *9.
186 Compl. ¶ 13; see also id. ¶ 125.
The basis for that knowledge is alleged to be a May 3, 2016 Board presentation
revealing “poor results of at least two—and potentially all three—of Zimmer’s 2016
North Campus internal audits.”187
The plaintiffs focus on a slide from that presentation that they say describes
the results of the March 31, 2016 and April 13, 2016 internal audit reports that listed
a total of four critical, 21 major, and two minor observations related to the North
Campus.188 That slide does not include the results of the June 7, 2016 audit report,
which was “in draft” form with the result “TBD.”189 Although the plaintiffs say that
copies of the internal audit reports “were provided to the Board no later than May 3,
2016,” there are no particularized facts pleaded in support.190 The plaintiffs are not
even certain that the information described on the slide corresponds to the three
North Campus audits in the first place.191
The difficulty for the plaintiffs is an absence of pleaded facts implying bad
faith on the part of the Director Defendants. Even if the court accepts as true that
the slide the plaintiffs highlight described the three North Campus internal audits,
187 Id. ¶ 159.
188 Id. ¶¶ 85, 124, 159. The slide the plaintiffs highlight lists the March 31, 2016 internal audit report as including 13 major and four minor observations. Id. ¶ 159. The plaintiffs, however, allege that only six major and two minor observations from that audit report relate to the North Campus. Id. ¶ 124. 189 Id. ¶ 159.
190 Id. ¶¶ 13, 18.
191 Id. ¶ 159 n.18.
there are no particularized allegations supporting a reasonable inference that the
Board knew the results of the North Campus internal audits would be spell
“disaster.”192 As with the prior time period, the North Campus is not singled out.
The results of 11 other audits at Zimmer facilities—all with some degree of critical,
major, and minor observations—are also included with the same level of detail.193
The plaintiffs acknowledge that the May 3, 2016 presentation was largely “[l]ike
other presentations before it” because it “led the Board on a global overview of all
of Zimmer’s FDA inspections during 2015 and 2016 to-date.”194
The Board presentation given at the next meeting on July 15, 2016 likewise
cannot support an inference of scienter. The plaintiffs again point to one slide from
the July 15, 2016 Board deck that they say indicated the “severity and scope of
Zimmer’s manufacturing problems” at the North Campus.195 More specifically, they
focus on one line of a six-line chart on a slide that lists “Network Remediation
Activities.”196 Over a dozen facilities are discussed, including “Warsaw Biomet
(2016/2017/2018)” (i.e., the North Campus) with the “Driver” for remediation
192 Id. ¶ 13; see also ¶¶ 159–161.
193 Id. ¶ 159.
194 Id. ¶ 158.
195 Id. ¶ 167.
196 Id. ¶ 166.
described as: “Corporate Audit and Zimmer Warsaw/Ponce lessons learned from
Form 483 Observations.”197
The plaintiffs make much of the fact that only the North Campus was
scheduled to have remediation efforts last into 2018.198 That may be so. But even
if the court were to deduce from that detail that the North Campus’ problems were
“not an easy set of issues to remediate”199 and would require a period of time to fully
address, it cannot reasonably follow that the Board knew they would escalate and
cause Zimmer to suffer financial harm in the future.200 Consequently, there is no
basis to infer that the Board intentionally “concealed” information about the internal
audits from stockholders by creating misleading public filings.201
Further, the Complaint lacks allegations suggesting Board-level involvement
in preparing the disclosures that satisfy the heightened pleading requirements of
Rule 23.1. The only disclosures that the plaintiffs challenge during this time period
are: (1) the second quarter 2016 Form 10-Q (filed with the SEC on August 8,
197 Id.; see also id. ¶ 187.
198 Id. ¶¶ 167, 187.
199 Id. ¶ 167.
200 See TrueCar, 2020 WL 5816761, at *15 (finding no scienter where the plaintiffs failed to allege facts demonstrating “that the directors in attendance at the meeting knew before they signed or approved” the challenged disclosure that the company’s “business . . . would suffer”). 201 Compl. ¶ 167.
2016),202 and (2) the prospectus supplements for the June and August Offerings
(filed with the SEC on June 13, 2016, June 15, 2016, August 9, 2016, and August
11, 2016, respectively).203 Beyond the sort of contentions about “causing” or
“approving” disclosures I previously found wanting,204 the only facts pleaded that
address the Board’s role in these disclosures relate to an August 5, 2021 Audit
Committee meeting where the August Offering was discussed.205 But there is no
allegation that the Audit Committee approved of the second quarter Form 10-Q or
the prospectus supplement for the August Offering at that meeting.206 “[F]actual
details” about “how the [B]oard was actually involved in creating or approving the
statements” are “crucial to determining whether demand on the [Board] would have
been excused as futile.”207 Without them, I cannot conclude that the Director
Defendants acted with scienter and face a substantial likelihood of liability for
202 Id. ¶ 215.
203 Id. ¶¶ 263, 265.
204 See supra at 38–40.
205 Compl. ¶ 172. The plaintiffs do not allege that the Audit Committee discussed any FDA compliance issues at that meeting, let alone the specific compliance issues at the North Campus. 206 Guttman, 823 A.2d at 498 (dismissing complaint that was “devoid of any pleading regarding the full board’s involvement in the preparation and approval of the company’s financial statements” and of “particularized allegations of fact demonstrating that the outside directors had actual or constructive notice of the accounting improprieties”). 207 Citigroup, 964 A.2d at 133 n.88.
material omissions or misstatements in the Form 10-Q or August Offering
documents.
c. After the September 12, 2016 Inspection
The primary harms alleged in this case began with the September 12, 2016
FDA inspection of the North Campus, which resulted in negative observations,
product ship holds, a Form 483, and preceded reduced revenue guidance and a
decline in Zimmer’s stock price. All of the PE Funds had exited their investments
at least a month before the inspection began. The plaintiffs’ focus largely is on
ordinary course SEC filings issued after the inspection, rather than filings connected
to the Offerings, during this time period.
The Board first learned about the commencement of the FDA’s inspection
during a regularly scheduled September 23, 2016 Board meeting.208 Zimmer
management told the Board that the inspection was “‘for cause’ based on product
complaints that had been received” and that the inspection would last for about two
weeks.209 There are no well-pleaded facts stating that the Board was told a facility
shut down or product ship hold had occurred or would occur.210 There is also no
208 Compl. ¶ 175.
209 Id.
210 The plaintiffs allege that the FDA inspection of the North Campus had “resulted in multiple product ship holds” by the time of the September 23, 2016 meeting. Id. ¶ 176. The plaintiffs do not allege, however, that the Board had any knowledge of these product ship holds.
reason to believe that the Board could have foreseen the ship hold, which plaintiffs
describe as a “rare consequence of an FDA inspection.”211 The Form 483 listing the
results of the FDA inspection was not issued until two months after the Board
meeting, on November 22, 2016.212
The first time that the plaintiffs allege with particularity that the full Board
learned of the fallout from the North Campus inspection is at a December 16, 2016
Board meeting.213 At oral argument, the plaintiffs clarified that they are challenging
certain disclosures that were issued before that December 16, 2016 meeting.214
Those disclosures appear to be: (1) Zimmer’s third quarter 2016 earnings release
(issued on October 31, 2016),215 (2) Dvorak’s statements to investors during an
earnings call (also on October 31, 2016),216 (3) Zimmer’s third quarter 2016 Form
10-Q (filed with the SEC on November 8, 2016),217 and (4) Zimmer’s December 14,
211 Id. ¶ 19. The plaintiffs do not allege that any Zimmer or Biomet facility had ever been subject to a product ship hold before September 29, 2016. 212 Id. ¶ 116. The Complaint lists the date of the Form 483 as November 20, 2016 (see id. ¶ 9) but that appears to be an error. 213 Id. ¶¶ 113, 184–88.
214 See Oral Arg. Tr. 72 (June 15, 2021) (Dkt. 105) (responding to the court’s question about what disclosures were challenged after September 12, 2016). 215 See Compl. ¶¶ 181–82.
216 See id. ¶ 218.
217 See id. ¶ 221.
2016 press release in which it mentioned “certain regulatory compliance gaps at the
legacy Biomet operation in Warsaw.”218
As with disclosures from the earlier time periods, there is ambiguity
around which misstatements or omissions in those disclosures the plaintiffs
believe are material. There are also no particularized allegations that would
suggest the Director Defendants had knowledge that the statements were
materially wrong before December 16, 2016. Of course, it is not unreasonable
to think that the Board would have been given updates on the North Campus
inspection and the product ship holds throughout the fall of 2016. But there
are no specific, factual allegations in the Complaint that would support such
an inference. Even if there were, the plaintiffs still must plead facts
demonstrating that the Board intentionally concealed that information from
the public by causing Zimmer to issue materially misleading disclosures.
They have not done so.
With the exception of the earnings release (which I will address next),
the plaintiffs do not describe any Board-level involvement in these
disclosures. They say nothing that could tie the directors to Dvorak’s October
31, 2016 statements. There is also no allegation that the Board had any
involvement in the press release, which could hardly evidence deceit in any
218 Id. ¶ 231.
event since it explained that Zimmer “ha[d] developed and [wa]s executing a
remediation plan to fully address the issues cited by the FDA.”219 As to the
third quarter Form 10-Q, the plaintiffs’ conclusory statement that Form 10-Q
was “reviewed and approved by the Audit Committee and Board” does not
satisfy Rule 23.1’s pleading requirements.220
The only challenged disclosure that comes close to directly implicating any of
the Demand Board members is the third quarter earnings release that was reviewed
and approved by the Audit Committee. The third quarter earnings release covered
the period ending September 30, 2016—just one day after the first ship hold went
into effect. It is uncertain how much, if at all, the ship hold affected Zimmer’s third
quarter results (or what the Audit Committee knew about potential effects).221 But
based on the Complaint, there is reason to infer that the Audit Committee members
219 Id. ¶ 231. The Complaint states that this press release was only a “partial public disclosure[].” Id. ¶ 184. The plaintiffs do not, however, allege with particularity what material facts were omitted. 220 Id. ¶ 221. See supra note 182 (citing cases); see also Citigroup, 964 A.2d at 134.
Like the earnings release discussed next, it is also not apparent that the Form 10-Q could support a finding of bad faith. That public filing announced that the company’s below-guidance revenues were due to “some temporary disruption in product supply . . . related to several factors.” Compl. ¶ 221. Those sorts of statements seem inconsistent with the plaintiffs’ cover-up theory. 221 On December 14, 2016, Zimmer disclosed that “the anticipated full impact of” the North Campus ship hold “was included in the Company’s sales and earnings guidance update issued on October 31, 2016.” Id. ¶ 231. The plaintiffs do not allege that this statement in particular was false or misleading.
knew that the FDA inspection of the North Campus would have an effect on
Zimmer’s revenue guidance when they approved the earnings release. As the
Complaint points out, the Audit Committee was given an update “on the ongoing
FDA inspection of [North] Campus” during its October 24, 2016 meeting.222 “At
the conclusion of [that] discussion, the Committee members expressed no objections
to the contents of the draft earnings release.”223
The earnings release cannot, however, support a finding that the Audit
Committee members face a substantial likelihood of liability for a duty of loyalty
claim. The plaintiffs’ allegations emphasize that the earnings release revealed
problems to the market. According to the Complaint, the earnings release “reduced
[Zimmer’s] revenue guidance for the fourth quarter of 2016, causing a massive
decline in the share price.”224 The plaintiffs describe the third quarter 2016
disclosures as painting “a drastically different outlook” than Zimmer had previously
222 Id. ¶ 181; Barillare Decl. Ex. 18.
223 Compl. ¶ 181; Barillare Decl. Ex. 18.
224 Compl. ¶ 23; see also id. ¶¶ 217, 223.
provided.225 It is difficult to square these allegations with the plaintiffs’ contention
that the directors were engaging “in a scheme to defraud Zimmer investors.”226
The plaintiffs nonetheless argue that the earning release was an attempt to
“hide and obscure” information from the public because the release “contained no
disclosure of the FDA inspection or manufacturing shutdown.”227 In other words,
the Audit Committee did not ensure that Zimmer adequately disclosed a potential
reason for its reduced guidance. That assertion might call into question the Audit
Committee members’ “‘erroneous judgment’ concerning the proper scope and
content of the disclosure.”228 But that would, at best, support an exculpated claim
225 Id. ¶ 217. It is also not apparent what about the earning release was false or misleading, given the more negative outlook that it presented. The roughly 14% decline in Zimmer’s stock price that the plaintiffs say demonstrates harm occurred weeks before the plaintiffs allege the market was informed about the Form 483 and ship holds at the North Campus. The plaintiffs do not allege that Zimmer’s stock price fell when the market learned about the Form 483 and the product ship hold at the North Campus on December 14, 2016. The final allegation in the Complaint about the effects on Zimmer’s stock price is that “[b]y November 14, 2016, Zimmer’s stock price reached a low of $97.99.” Id. ¶ 223. The dearth of allegations demonstrating any negative reaction to the disclosure of events at the North Campus further undercuts the plaintiffs’ argument that those events were material ones requiring disclosure beyond the financial information Zimmer released at the end of the third quarter. Notably, the December 14, 2016 press release quoted in the Complaint states that the “full impact” of various matters including the North Campus inspection and Form 483 was “included in the Company’s sales and earnings guidance update issued on October 31, 2016.” Id. ¶ 231. 226 See Pls.’ Answering Br. 6.
227 Id. at 17–18.
228 Orman v. Cullman, 794 A.2d 5, 41 (Del. Ch. 2002) (quoting Crescent/Mach I P’rs, L.P. v. Turner, 846, A.2d 963, 987 (Del. Ch. 2000)); see also Morrison v. Berry, 2019 WL 7369431, at *18 (Del. Ch. Dec. 31, 2019) (“Bad faith, in the context of omissions, requires
for breach of the directors’ duty of care.229 An inference cannot be drawn, from the
limited allegations in the Complaint, that the Audit Committee approved an earnings
release reducing revenue guidance while intentionally omitting material information
about a possible underlying cause.230 The plaintiffs do not ascribe any bad faith
actions or motives to the Audit Committee members that would demonstrate
otherwise.
* * *
To summarize, the Complaint lacks particularized factual allegations
supporting a reasonable inference that any Director Defendant faced a substantial
likelihood of liability for a disclosure claim under Malone. There are no
particularized allegations that the directors knew that the North Campus was facing
atypical compliance struggles that would have a materially negative effect on
Zimmer’s financial performance until late 2016. The PE Funds had already exited
their investments in Zimmer by that point and, given the lack of any alleged ties
between a majority of the Demand Board and the PE Funds, why the directors would
that the omission be intentional and constitute more than an error of judgment or gross negligence.”). 229 Id.
230 See Malone, 722 A.2d at 14 (explaining that a disclosure violation must be made “in bad faith, knowingly or intentionally”); cf. infoUSA, Inc. S’holders Litig., 953 A.2d 963, 990 (Del. Ch. 2007) (explaining that directors violate their fiduciary duties “where it can be shown that the directors involved issued their communication with the knowledge that it was deceptive or incomplete”).
“conceal” problems at North Campus is not apparent or alleged. The plaintiffs only
sufficiently allege Board-level involvement in one disclosure after the directors
gained some knowledge of the significance of the North Campus’s compliance
issues: the third quarter 2016 earnings release approved by the Audit Committee.
That earnings release, however, could support an exculpated duty of care claim at
the most. The plaintiffs’ disclosure arguments are insufficient to establish a
substantial likelihood of liability for a non-exculpated claim. Demand is therefore
not excused for a single Demand Board member on the basis of alleged disclosure
violations.
2. “Knowing Facilitation” of Insider Trading
The plaintiffs next argue that demand is futile because the Director
Defendants who constitute a majority of the Demand Board face a substantial risk
of liability in connection with the plaintiffs’ Brophy claim. To state a Brophy claim,
a plaintiff must plead that insiders (1) “possessed material, nonpublic company
information” and (2) “used that information improperly by making trades because
[they were] motivated, in whole or in part, by the substance of that information.”231
The plaintiffs do not allege that any director personally sold stock in the
Offerings. They do not allege that the PE Funds (or anyone else) controlled a
majority of the Demand Board. The only Demand Board member who the plaintiffs
231 In re Oracle Corp., 867 A.2d 904, 934 (Del. Ch. 2004).
say “personally benefitted” from the PE Funds’ stock sales is Michelson, through
his affiliation with the KKR Fund.232 Michelson is also the only member of the
Demand Board named as a defendant on the plaintiffs’ insider trading claim.233
The plaintiffs contend that the six Director Defendants face liability because
they “knowingly facilitated” the PE Funds’ insider trading by “approving the
offerings.”234 The plaintiffs argue that “knowing facilitation” is evidenced by the
directors “signing (and disseminating) the Registration Statement and related
documents.”235 This is simply another iteration of the plaintiffs’ disclosure claim.
The plaintiffs’ limited and conclusory allegations about Board-level involvement in
the Registration Statement and prospectus supplements cannot support an inference
of knowledge, and resulting scienter, for a Brophy claim just as they cannot support
a non-exculpated disclosure claim.236
232 Pls.’ Answering Br. 47.
233 See Compl. ¶¶ 343–48.
234 Pls.’ Answering Br. 47.
235 Id. at 47–48.
236 See supra at 37–41; cf. In re Fitbit Inc. S’holder Deriv. Litig., 2018 WL 6587159, at *13, *18 (Del. Ch. Dec. 14, 2018) (finding that a director “knowingly facilitated” insider trading where the complaint adequately alleged that a majority of the demand board knew that “the information at issue was material and nonpublic”); In re Emerging Commc’ns, Inc. S’holders Litig., 2004 WL 1305745, at *39 (Del. Ch. May 3, 2004) (explaining that a director was “culpable because he voted to approve the transaction even though he knew, or at the very least had strong reasons to believe, that the . . . merger price was unfair”).
The plaintiffs’ other theory of “knowing facilitation” of insider trading is that
the Director Defendants approved the Offerings, “including a $250 million
repurchase on the February [O]ffering” and, “with respect to the August 2016
[O]ffering, grant[ed] waivers of the lock-up agreement which permitted the Private
Equity Defendants to sell their shares earlier.”237 For support, the plaintiffs rely on
this court’s decision in In re Fitbit Inc. Stockholder Derivative Litigation.238 The
plaintiffs’ argument fails for several reasons.
First, to show that the Director Defendants knowingly permitted insider
trading by approving the Offerings, the plaintiffs must allege particularized facts
supporting an inference that the directors knew that the PE Funds received material
non-public information and that their sales were based on that information. 239 That
the Board knew about compliance issues before the Offerings is irrelevant.240 The
plaintiffs must plead that the Board knew that the PE Funds also had that material
non-public information before selling their Zimmer shares in the Offerings.
237 Pls.’ Answering Br. 47–48.
238 2018 WL 658715.
239 See Guttman, 823 A.2d at 505; Stepak v. Ross, 1985 WL 21137, at *5 (Del. Ch. Sept. 5, 1985). 240 See Pls.’ Answering Br. 48 (arguing that the Complaint “pleads chapter and verse about the knowledge of Zimmer’s systemic manufacturing failures possessed by the Director Defendants before the Offerings and throughout the relevant period leading up to the FDA inspection”).
The plaintiffs contend that Michelson and Rhodes, “as agents of their
respective funds,” must have shared with the PE Funds the information about
Zimmer’s compliance challenges that they learned during Zimmer Board
meetings.241 That is so, according to the plaintiffs, because “under the terms of the
Stockholders Agreement, Michelson and Rhodes were assigned to the Board for the
express purpose of representing the interests of the [PE Funds] . . . and sharing with
them confidential Zimmer information.”242 These allegations are entirely
conclusory. In the Securities Class Action, the federal court rejected a similar
argument, finding there was no allegation in that case “that any information relating
to problems at North Campus was in fact shared with the Private Equity Defendants,
whether in this instance or any others.”243 Instead, the plaintiff there had alleged
only that “the Private Equity Defendants had potential access to information,”244
which is “not the same as actually possessing the specific information and knowing
it.”245
241 Id. at 71.
242 Id. at 69.
243 Shah, 348 F. Supp. 3d at 849.
244 Id.
245 Id. (quoting Plumbers & Pipefitters Local Union 719 Pension Fund v. Zimmer Hldgs., Inc., 2011 WL 338865, at *21 (S.D. Ind. Jan. 28, 2011), aff’d, 679 F.3d 952 (7th Cir. 2012)).
The Complaint here has the same flaw. It discusses the potential for the PE
Funds to access information based on the Stockholders Agreement. There are no
particularized allegations that Michelson or Rhodes actually shared any information
with the PE Funds. Moreover, even if the court were to infer that Michelson and
Rhodes shared material non-public information with the PE Funds, the Complaint
lacks any basis to infer that the rest of the Board had knowledge regarding this
alleged information sharing.246
The plaintiffs also do not allege that the Board knew the PE Funds’ sales were
based on knowledge of Zimmer’s compliance issues. The fact that the Board
“approved” the Offerings is not enough to demonstrate scienter. The plaintiffs try
to bolster their argument by arguing that the Board “grant[ed] waivers of the lock-
up agreement”247 as evidence of knowing facilitation, which was a focus of this
court’s decision in Fitbit.248 But the Complaint mentions a lock-up agreement only
once, noting that the “Defendants further facilitated the Private Equity Defendants’
illegal stock sales by . . . waiving the lockup provision for the August 2016
246 In Fitbit, a majority of the demand board sold stock either personally or “through their controlled funds.” Fitbit, 2018 WL 6587159, at *14. The court in that case did not need to consider whether information shared with the board was subsequently shared with outside entities that were connected to a single member of the demand board or whether a majority of the demand board knew that information was shared. 247 Pls.’ Answering Br. 47.
248 See Fitbit, 2018 WL 6587159, at *17–18.
offering.”249 There is nothing else pleaded about a lock-up. The Complaint does not
explain what “lockup provision” the plaintiffs are referring to, when it was
implemented, who implemented it, or how (when, or by whom) it was waived.250
The plaintiffs’ allegations that the Board “approv[ed] a $250 million stock
repurchase in the February 2016 offering” are equally conclusory.251 The Complaint
does not include any particularized facts regarding the Board’s involvement in the
stock repurchase, when the Board voted to approve the stock repurchase, or the
249 Compl. ¶ 318.
250 To better understand the plaintiffs’ allegations, I reviewed the publicly-filed prospectuses related to the June and August Offerings, which provide that Zimmer was subject to and lacked the power to waive a lock-up agreement. See Compl. ¶ 263 (referencing the June 13, 2016 and June 15, 2016 prospectus supplements). Specifically, on June 13, 2016, the Company filed a free writing prospectus which provided that Zimmer and certain officers and directors affiliated with the PE Funds would enter into a 60-day lockup after the June Offering. Zimmer Biomet Hldgs., Inc., Free Writing Prospectus (Form FWP) (June 13, 2016) (“As part of the offering, Zimmer Biomet, its chief executive officer and chief financial officer and certain of its directors and stockholders affiliated with KKR, Goldman Sachs and TPG will enter into lock-up agreements with respect to the sale of shares of common stock of Zimmer Biomet for a 60-day period following the offering, subject to customary exceptions.”). Based on Zimmer’s June 15, 2016 final prospectus supplement for the June Offering, it appears to me that the lock-up agreement relevant to the August Offering could only be waived by “Goldman, Sachs & Co. and J.P. Morgan Securities LLC,” not the Company or the Board. Zimmer Biomet Hldgs., Inc., Prospectus Suppl. S-7 (Form 424B7) (June 15, 2016) (“Pursuant to the foregoing lock-up agreements, at any time and without notice, Goldman, Sachs & Co. and J.P. Morgan Securities LLC may release all or any portion of our common stock subject to the lock-up agreements.”); id. at S-16 (explaining that pursuant to the lockup agreements the relevant parties could not trade “without the prior written consent of Goldman, Sachs & Co. and J.P. Morgan Securities LLC” (emphasis added)). These filings further cut against the plaintiffs’ assertion that “granting waivers of the lock-up agreement” creates a substantial likelihood of liability for the Director Defendants. 251 Compl. ¶ 318.
Board’s composition at that time. These indefinite statements fall short of Rule
23.1’s pleading requirements and provide no basis for the court to draw an inference
of scienter for the Director Defendants. As a result, at least 10 members of the
Demand Board cannot be found to face a substantial likelihood of liability for
knowingly facilitating insider trading.
3. The Caremark Claim
The plaintiffs next argue that a majority of the Demand Board faces a
substantial likelihood of liability under Caremark for failing to “[e]nsure FDA
[c]ompliance.”252 Despite adopting certain phrases from Caremark’s progeny and
asserting that the Board had “actual knowledge of ‘mission critical’ regulatory
compliance failures,”253 none of the counts in the Complaint are based on an
oversight claim. Instead, the basis for any potential Caremark liability appears to
be a hypothetical one raised for the first time in the plaintiffs’ answering brief. At
argument, counsel for the plaintiffs’ stated that “the complaint could encompass a
Caremark claim.”254
Even if I were to read a loosely pleaded Caremark claim from the allegations
in the Complaint, it would not create a substantial likelihood of liability for the
252 Pls.’ Answering Br. 50.
253 Compl. ¶ 302.
254 Oral Arg. Tr. 56 (emphasis added).
Director Defendants. A Caremark claim would have required the plaintiffs to plead
particularized facts showing that either (1) “the directors utterly failed to implement
any reporting or information system or controls” or that (2) “having implemented
such a system or controls, [the directors] consciously failed to monitor or oversee its
operations thus disabling themselves from being informed of risks or problems
requiring their attention.”255 The Complaint is, on its face, inconsistent with a claim
under either prong of Caremark.
First, rather than plead that Zimmer lacked a Board-level system of internal
controls, the Complaint details the oversight systems in place to address regulatory
compliance issues. For example, the plaintiffs allege that the Audit Committee was
responsible for “the Company’s compliance with legal and regulatory requirements,
including oversight of the Company’s Corporate Compliance Program.”256 The
Complaint also describes the Board’s oversight of regulatory compliance at multiple
meetings where it received updates on FDA inspections and voluntary internal audits
at Zimmer’s facilities.257
255 Reiter v. Fairbank, 2016 WL 6081823, at *7 (Del. Ch. Oct. 18, 2016).
256 Compl. ¶ 78.
257 See id. ¶¶ 127–93 (alleging that the Zimmer Board met at least a dozen times between 2015 and 2018 and regularly received updates “giving the Board a global overview of all of the Company’s FDA inspection results” and highlighting compliance related developments); see also id. ¶ 8.
Any argument under the second prong of Caremark is also contradicted by
the allegations in the Complaint. The plaintiffs repeatedly allege that Zimmer
actively undertook remediation efforts to resolve compliance issues such as Project
Trident, “a long-running FDA compliance remediation program at several legacy
Zimmer facilities.”258 They describe multiple attempts to cure ongoing FDA
violations and regular updates to the Board.259 The story the plaintiffs tell in the
Complaint is a far cry from being about a board of directors ignoring “red flags.”260
Because none of the members of the Demand Board face a substantial
likelihood of liability for a Caremark claim, demand is not excused on that basis.
4. The Securities Class Action
The plaintiffs’ final demand futility argument is that eight of the 11 Demand
Board members faced “live claims” as defendants in the Securities Class Action at
the time this action was filed.261 In Pfeiffer v. Toll, this court found that demand was
258 See, e.g., id. ¶¶ 109, 123, 128, 138, 158, 177.
259 See, e.g., supra at 10–16, 22–23 (describing Board presentations).
260 The plaintiffs argue in their brief that these remediation efforts were “an abject failure as the systemic problems were not being corrected, the purported remediation was repeatedly delayed and subject to massive cost overruns, and most importantly did not protect the Company from additional and ongoing FDA compliance problems for years.” Pls.’ Answering Br. 50 n.20. Such second-guessing also cannot form the basis of a Caremark claim. See, e.g., Stone v. Ritter, 911 A.2d 362, 370 (Del. 2006); In re Caremark Int’l Inc. Deriv. Litig., 698 A.2d 959, 971 (Del. Ch. 1996); In re Gen. Motors Deriv. Litig., 2015 WL 3958724, at *1, *17 (Del. Ch. June 26, 2015); Citigroup, 964 A.2d at 127–29. 261 Pls.’ Answering Br. 51; see Compl. ¶¶ 321–25.
futile where a majority of the demand board faced a substantial likelihood of liability
for alleged misconduct in a pending parallel securities action.262 To support their
argument that facts like those in Pfeiffer are present in this case, the plaintiffs focus
on the denial of the defendants’ motion to dismiss in Shah.263 But in Pfeiffer—unlike
here—the federal complaint survived “under the rigorous standards for pleading
securities fraud” and raised a “powerful and cogent inference of scienter” against the
director defendants.264
The plaintiffs here seize on language the federal court in the Securities Class
Action used to characterize the federal plaintiff’s allegations as telling a tale of
“fraud” and describing the defendants as “knowingly sitting on a proverbial ticking
time bomb of a factory known as North Campus.”265 It is not clear whether the
262 989 A.2d 683 (Del. Ch. 2010), abrogated on other grounds by Kahn v. Kohlberg Kravis Roberts & Co. L.P., 23 A.3d 831 (Del. 2011). 263 See Compl. ¶¶ 323–25.
264 Pfeiffer, 989 A.2d at 690.
265 Shah, 348 F. Supp. 3d at 826–27. The “time bomb” quotation—pulled from the introduction of the opinion—does not specify whether the comments regarding fraud applied to all defendants or only to those who were subject to claims requiring a finding of fraud. Dealing with similarly vague language, the court in TrueCar declined to find the related securities action sufficient to impugn the board’s impartiality. See TrueCar, 2020 WL 5816761, at *22 (finding that “it is unclear from the paragraph quoted above containing the district court’s analysis in the Securities Class Action whether its comments concerning scienter were intended to apply to all defendants in that action or—as would be logical—only to those who were the subject of scienter-based claims” (emphasis added)). The court similarly expressed skepticism that strict liability claims would compromise defenses to non-exculpated duty of loyalty claims, which require evidence of bad faith. Id. (“As for Plaintiffs’ argument, it also is unclear what ‘factual defenses’ a director would fear having compromised in a case that only asserts claims for strict liability
sentences from the Shah decision that the plaintiffs draw attention to were intended
to apply to all defendants in that action. But the only claims in the Securities Class
Action against the Director Defendants here were for violations of Sections 11 and
15 of the Securities Act.266 As the plaintiffs acknowledge, “Sections 11 and 15 of
the Securities Act . . . are strict liability statutes that do not require a showing of
scienter.”267
Given Zimmer’s exculpation provision, the plaintiffs must demonstrate that
the directors acted with scienter, “i.e., there was an ‘intentional dereliction of duty’
or ‘a conscious disregard’ for their responsibilities, amounting to bad faith.”268 Strict
liability under Section 11 or Section 15 of the Securities Act alone cannot meet this
high bar.269 It has no bearing on whether the directors acted in good faith. The
and negligence against him, for which the director would be exculpated from personal liability.”). 266 See Shah, 348 F. Supp. 3d at 827; Second Am. Class Action Compl. for Violations of the Federal Securities Laws, Shah v. Zimmer Biomet Hldgs., Inc., 348 F. Supp. 3d 821 (N.D. Ind. 2018) (No. 3:16-cv-00815-PPS-MGG), 2017 WL 5494812, ¶¶ 454–59, 468–81, 490–97 (Dkt. 60). 267 Pls.’ Answering Br. 51.
268 Goldman Sachs Gp., 2011 WL 4826104, at *12 (quoting In re Walt Disney Co. Deriv.
Litig., 907 A.2d 693, 755 (Del. Ch. 2005), aff’d, 906 A.2d 27 (Del. 2006)). 269 See TrueCar, 2020 WL 5816761, at *21 (finding that the presence of an “exculpatory charter provision and the absence of scienter-based claims against the Demand Board directors named in the Securities Class Action” meant that a majority of the demand board “would not face a substantial likelihood of personal liability in that action so as to compromise their ability to impartially consider a demand”); In re LendingClub Corp. Deriv. Litig., 2019 WL 5678578, at *15 (Del. Ch. Oct. 31, 2019) (holding that “[l]iability
claims in the Federal Securities Action therefore cannot provide a basis to conclude
that the Demand Board members named as defendants in Shah were unable to
impartially consider a demand when this action was filed.
Relying on Fitbit once again, the plaintiffs argue that the Shah court’s factual
statements are probative of demand futility, even though the securities claims
sustained against the directors were non-scienter based.270 But in Shah, the scienter
analysis only addressed the states of mind of officer defendants who faced Section
10(b) claims.271 There were no “holistic” allegations that “suffice[d] to establish
scienter” for the Director Defendants.272 Furthermore, in Fitbit, the findings in the
related federal action reinforced the court’s conclusion that knowledge had been
sufficiently pleaded against a majority of the Fitbit demand board.273 As I previously
discussed, there are no well-pleaded allegations of Board-level scienter in the
Complaint that the Shah decision could bolster.
under Section 11 would not, in and of itself, have gotten to the heart of whether the directors acted in bad faith concerning wrongdoing at issue in both actions”). 270 Pls.’ Answering Br. 52.
271 Cf. Pfeiffer, 989 A.2d at 690 (finding demand futile based, in part, on federal court decision holding that the same individual defendants acted with scienter regarding “the same trades at issue” in the Delaware action). 272 Fitbit, 2018 WL 6587159, at *16.
273 Id. at *16–17.
III. CONCLUSION
For the reasons described above, the plaintiffs have failed to establish that
making a demand on the Zimmer Board would have been futile. At least eight
members of the eleven-member Demand Board could have impartially considered a
demand to pursue this action on Zimmer’s behalf. As such, the defendants’ motions
to dismiss the Complaint pursuant to Court of Chancery Rule 23.1 are granted. The
Complaint is dismissed with prejudice in its entirety.
In re Zimmer Biomet Holdings, Inc. Derivative Litigation (In re Zimmer Biomet Holdings, Inc. Derivative Litigation) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.