Suzuki v. Abiomed, Inc.

943 F.3d 555
CourtCourt of Appeals for the First Circuit
DecidedNovember 27, 2019
Docket19-1233P
StatusPublished
Cited by9 cases

This text of 943 F.3d 555 (Suzuki v. Abiomed, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the First Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Suzuki v. Abiomed, Inc., 943 F.3d 555 (1st Cir. 2019).

Opinion

United States Court of Appeals For the First Circuit

No. 19-1233

KEISUKE SUZUKI,

Plaintiff, Appellant,

v.

ABIOMED, INC.,

Defendant, Appellee.

APPEAL FROM THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MASSACHUSETTS

[Hon. Denise J. Casper, U.S. District Judge]

Before

Lynch, Selya, and Barron, Circuit Judges.

William T. Harrington, with whom Christine A. Maglione and Harrington Law, P.C. were on brief, for appellant. Kenneth M. Bello, with whom Alexandra D. Thaler and Bello Welsh LLP were on brief, for appellee.

November 27, 2019 SELYA, Circuit Judge. This case involves a claimed

breach of the implied covenant of good faith and fair dealing

brought by a former executive who contends that his quondam

employer, a producer of heart pumps, terminated his employment,

allegedly to deprive him of a sizable equity incentive. Because

the plaintiff has failed to present sufficient evidence that this

equity incentive constituted compensation already earned by virtue

of his past work under state law, we affirm the district court's

entry of summary judgment in the defendant's favor. The tale

follows.

I. BACKGROUND

We rehearse the facts and travel of the case, viewing

those facts in the light most flattering to the summary judgment

loser (here, the plaintiff). See Flovac, Inc. v. Airvac, Inc.,

817 F.3d 849, 852 (1st Cir. 2016). Defendant-appellee Abiomed,

Inc. designs, manufactures, and markets temporary mechanical

circulatory support devices, including the Impella line of heart

pumps. In early 2009, plaintiff-appellant Keisuke Suzuki started

consulting with Abiomed about the company's efforts to secure

Japanese regulatory approval for its Impella devices. The approval

process involves the submission of an application — known as the

Shonin application — to Japan's Pharmaceutical and Medical Device

Agency (PMDA). Submission of the Shonin application typically is

followed by various tests, audits, and expert panel reviews.

- 2 - Thereafter, the PMDA makes a recommendation to the so-called Upper

Panel of Japan's Ministry of Health, Labour and Welfare (MHLW).

Once the Upper Panel's review is complete, the MHLW announces its

final decision regarding approval.

In April of 2010, Suzuki began to work full-time as

Abiomed's vice-president of Asia — a position in which he assumed

primary responsibility for shepherding the Impella devices through

the Japanese regulatory approval process. His employment was

memorialized by an offer letter and a nondisclosure agreement. In

addition to a base salary, an annual bonus potential, and a

commission opportunity, the offer letter outlined three equity

awards to be paid upon the achievement of certain milestones en

route to regulatory approval: first, the issuance of 10,000 shares

of Abiomed common stock upon the submission of the Shonin

application; second, the issuance of 20,000 shares "when the MHLW

approve[d] Impella for general use"; and third, the issuance of

15,000 shares when Abiomed gained "[a]pproval for [the] targeted

reimbursement level of Impella."

Withal, the offer letter contained several caveats. To

begin, it stated that in order to receive the equity awards, Suzuki

must be actively employed by Abiomed when the relevant milestone

was achieved. Additionally, Abiomed "reserve[d] the right on a

prospective basis to modify, change or eliminate its

[c]ompensation, [b]onus or [b]enefit programs." Last but not

- 3 - least, the offer letter admonished that it was not to be "construed

as an agreement, either express or implied, to employ [Suzuki] for

any stated term," and it in no way altered Abiomed's policy "under

which both [Suzuki] and [Abiomed] remain[ed] free to end the

employment relationship at any time and for any reason."

On the advice of a friend who was also an attorney,

Suzuki requested the insertion of a provision to the effect that

if his employment was terminated without cause, he would retain

"the right to claim the equity" as long as a particular milestone

was achieved "within 6 months of [his] departure, as the majority

of the work would be done before that." Suzuki added that a

provision allowing him to claim the equity if a milestone was

achieved within three months after his dismissal would also be

"reasonable." Frank LeBlanc, Abiomed's chief human resources

official, responded that Abiomed declined to accommodate this

request, as its policy with respect to event-based equity

incentives entailed "grant[ing] those shares only after the event

has occurred, and only to active employees." Suzuki backed off,

replying: "Fair enough. I had to ask." He proceeded to sign the

offer letter that same day.

Eight days later, Suzuki executed the nondisclosure

agreement. This agreement provided, in pertinent part, that

Abiomed could terminate Suzuki's employment at any time with or

without cause during the first six months of his tenure.

- 4 - Thereafter, Abiomed could discharge him without cause only upon

twenty-eight days' written notice. Relatedly, the agreement

allowed Suzuki to resign his employment without cause at any time

upon twenty-eight days' written notice.

Around the same time that he assumed his new role, Suzuki

estimated that the Shonin application would be submitted by August

of 2010 and that approval of the Impella devices would take

approximately two years. These predictions proved overly

optimistic, and it was not until late March of 2011 that Abiomed

submitted the Shonin application and (in accordance with the 2010

offer letter) issued 10,000 shares of its common stock to Suzuki.

Between 2011 and 2014, Suzuki and his co-workers responded to well

over one hundred questions posed by the PMDA. During this period,

Suzuki's projected timeline for approval shifted. In periodic

presentations to Abiomed executives between 2011 and 2013, Suzuki

indicated that approval would occur in one to two years. On at

least two occasions, Suzuki intimated to colleagues that the PMDA

was poised to approve the Impella devices — but approval

nonetheless remained elusive.

The parties hotly dispute the reasons for this sluggish

pace. Suzuki maintains that Abiomed failed to prioritize the

Japanese approval effort, while various Abiomed executives stated

in depositions and affidavits that Suzuki's caustic style and

aggressive tactics stunted progress. This criticism does not

- 5 - appear to have come out of thin air: the record contains ample

uncontroverted evidence of abrasive e-mails from Suzuki to Abiomed

executives, together with evidence that Suzuki stormed out of at

least three meetings with colleagues during his five-year tenure.

Equally concerning, Abiomed learned in January of 2015 that

Yoshimasa Yokoyama, the PMDA's lead reviewer of Abiomed's Shonin

application, had reported that "bad rumors" were circulating about

Suzuki. These rumors depicted Suzuki as telling a "biased story"

about the Impella devices, "blaming PMDA for delay," and recruiting

Japanese physicians to pressure regulators for approval (a tactic

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943 F.3d 555, Counsel Stack Legal Research, https://law.counselstack.com/opinion/suzuki-v-abiomed-inc-ca1-2019.