TIMOTHY J. CORRIGAN, District Judge.
In this bifurcated action, a jury previously ruled that Defendants Zassi Holdings, Inc. and Peter von Dyck committed breach of contract and fraud in the course of selling business technology to Plaintiff Hollister Incorporated. Now in the non-jury damages phase, Hollister attempted to prove that but for these transgressions, it would have prevailed in a patent infringement suit against its main competitor, ConvaTec, Inc., and thus seeks to collect from Zassi and von Dyck the patent damages it would have won from ConvaTec.
Hollister is an independently-owned global company that develops, manufactures, and markets health care products, including ostomy, continence, critical care (including bowel management), and wound care products. Zassi is a privately-held company that designs, develops, manufactures, and commercializes medical devices.
In 2006, Hollister purchased the technology and intellectual property rights related to a bowel management system ("BMS") developed by Zassi and von Dyck, Zassi's founder and chief executive officer. Under the Asset Purchase Agreement (Pl. Ex. 38), Hollister paid Zassi $35 million to acquire certain assets, including Zassi's interest in the patent applications that resulted in U.S. Patent Nos. 7,147,627 ("`627 patent"), which issued on December 12, 2006 (Pl. Ex. 53), and 7,722,583 ("`583 patent"), which issued on May 25, 2010 (Pl. Ex. 54).
Shortly thereafter, Hollister began manufacturing, marketing, and selling Zassi's BMS device and rebranded it the ActiFlo device. During this time, Hollister competed in the BMS marketplace with ConvaTec, a global company in the business of making and selling health care products, including ostomy devices and BMSs. Like Hollister, ConvaTec sold fecal management systems ("FMS"), including its Flexi-Seal device and its subsequently released Flexi-Seal Signal device ("Signal") (referenced in combination as the "ConvaTec products").
On October 7, 2010, shortly after the `583 patent had been issued, Hollister sued C.R. Bard, Inc. and ConvaTec, its two main competitors in the BMS space, alleging that their products infringed at least one of the claims of the `583 patent.
ConvaTec, however, asserted that Hollister's claim was barred by a settlement agreement executed between ConvaTec and Zassi in 2005 (before Hollister acquired the patent rights from Zassi), which released ConvaTec from present and future claims for infringement as to the Flexi-Seal device.
In Hollister's estimation, but for the release in the agreement between ConvaTec and Zassi, which Hollister only learned of in 2010 after it sued ConvaTec for patent infringement, Hollister would have obtained a substantial damages award against ConvaTec. Therefore, following its unsuccessful suit against ConvaTec, Hollister sued Zassi and von Dyck, claiming that Zassi breached the warranty of good and marketable title contained in the Asset Purchase Agreement (Doc. 1 ¶¶ 42-49), and that Zassi and von Dyck committed fraud by failing to disclose that Zassi had released claims against ConvaTec that would make it impossible for Hollister to enforce the patent rights it acquired from Zassi. (
The Court bifurcated the liability issues from damages for trial purposes. (Doc. 26). The measure of Hollister's damages was more distinct from the liability issues than in the usual case because Hollister's damages involved complex proof of patent infringement by ConvaTec, a non-party, and the amount of any resultant patent damages.
The liability issues were tried to a jury on February 4 through February 7, 2014 before the Honorable Paul A. Magnuson.
Shortly after the completion of the liability trial, Zassi and von Dyck's attorneys withdrew. (Doc. 84). New counsel appeared for Zassi and von Dyck, and after unsuccessfully moving for a retrial, also withdrew. (Docs. 89, 138, 139, 144). After no new counsel appeared, Hollister filed a Motion for Default Against Zassi Holdings, Inc. (Doc. 147), and a clerk's default was entered against Zassi on September 4, 2015 (Docs. 149, 150). New counsel later appeared on October 2, 2015 on behalf of von Dyck only to contest damages. (Doc. 153).
Before the trial on damages, the Court issued its
The Court has reviewed the extensive record, examined the evidence presented at trial,
Hollister asserts five claims from the patent in suit: claims 1, 2, 3, 4, and 6 of the `583 patent. (Tr. I, 105:1-3). The asserted claims relate to a BMS used to contain and divert fecal matter for bedridden, incontinent patients. (Pl. Ex. 54). The device is composed of a rectal catheter with various sections, each with different elasticity and durometer hardness, and may be used to facilitate the collection of fecal matter for patients requiring stool management, provide access for colonic irrigation, and provide a conduit through which medications may be administered. (
Hollister contends that the evidence establishes that the ConvaTec products meet every limitation in the five asserted claims. (Doc. 186 at 8-13; Tr. I, 137-61). Russell Genet, a patent lawyer and partner in the law firm of Nixon Peabody, testified on Hollister's behalf as its expert witness on both patent infringement and damages. (Tr. I, 75:2-3).
Von Dyck asserts that the ConvaTec products do not meet the claim limitations, arguing that claim 1 requires a rectal catheter with at least two distinct sections and varying durometer hardness. (Doc. 189 at 11). Von Dyck contends that the ConvaTec products do not have a rectal catheter with a first and second section as required by claim 1; instead, they have a single catheter tube, and as a result do not infringe claim 1. He relies primarily on the `583 patent's specifications, claim differentiation, and prosecution history to support this theory. Von Dyck declined to retain an expert witness to testify on his behalf, instead using the cross-examination of Genet to elicit testimony to support his non-infringement arguments.
Infringement analysis involves two steps: (1) claim construction, and (2) comparison of the properly construed claims to the accused devices.
The core of von Dyck's theory of non-infringement is that the ConvaTec products contain a single catheter tube, while the asserted claims of the `583 patent require a catheter tube with at least two distinct sections. Although von Dyck attempted to elicit testimony supporting his non-infringement arguments through the cross-examination of Genet, he failed to do so.
Von Dyck relies on the `583 patent's specifications
It is true that a district court may engage in claim construction during various phases of litigation, not just in a
In his Post-Trial Proposed Findings of Fact and Conclusions of Law, von Dyck notes that the `583 patent contains several references to sections of the rectal catheter as being distinct, each having a first and second end, connected to other sections of the rectal catheter, and having varying durometer hardness. (Doc. 189 at 7). Specifically, he references the abstract, the summary of the invention, and the detailed description. (
Although von Dyck attempted to present evidence through cross-examination that claim 1 of the `583 patent requires two distinct sections, Genet's testimony belies these efforts. He stated that "the specification in the file history, I don't think requires this type of design, the [two-section] design in the [Hollister] ActiFlo . . . where you actually have . . . different materials that are glued together as very separate pieces. I don't think that that's required by the patent." (Tr. II, 170:14-19). Further, he testified that "there's no language that would say — in the spec [specification] that would say that you have to make this device with two very different sections of different material of different durometers." (Tr. II, 173:9-12).
In fact, the Hollister ActiFlo's two-section catheter tube is simply a "preferred embodiment." (Tr. II, 173:12). In other words, under the limitations of claim 1, a party may make a catheter tube with one section of one durometer hardness and infringe that claim, even though the preferred embodiment, such as the ActiFlo device, comprises two sections. ConvaTec did so with the Flexi-Seal. Genet explained the way in which ConvaTec's Flexi-Seal has distinct sections, even though it is made of one silicone tube and has the same material from start to end: "[T]here is a distinct section of [the ConvaTec] catheter that is within the patient's rectal vault" and "there's also a distinct section of this catheter that transverses the . . . sphincter region." (Tr. II, 170:3-7). Thus, he opined that there are "distinct sections . . . of the ConvaTec product when you look at how it is used in a patient." (Tr. II, 170:10-11). Upon further questioning by the Court, Genet explained that while the preferred embodiment sold by Hollister contains multiple sections, "the claims don't require it to be made that way." (Tr. II, 171).
The claims of the patent define the invention, and it is improper for the Court to read into those claims limitations that simply are not there. 35 U.S.C. § 112;
While ConvaTec has succeeded in constructing a catheter tube that is different from Hollister's commercial embodiment of its invention, or even the embodiments described in the patent specifications, ConvaTec's invention nevertheless falls within the scope of Hollister's claim, which defines the scope of Hollister's right to exclude. The accused devices—here, the ConvaTec products—must be compared to the claim language as interpreted.
Von Dyck also argues that the infringement position Hollister took in this case regarding claim 1 is inconsistent with the position it was required to take to get the `583 patent issued, and thus Hollister should be estopped from asserting infringement of claim 1. (Tr. II, 156:19-23). At trial, von Dyck guided Genet through amendments in the file wrapper
To the extent that von Dyck contends that Hollister is barred by prosecution history estoppel from asserting that claim 1 does not require distinct sections, this theory is inapplicable because Hollister does not assert a theory of infringement under the doctrine of equivalents.
Similarly, to the extent von Dyck construes his argument as one of prosecution disclaimer, there is insufficient proof that Hollister (or its predecessors) made an unambiguous disavowal of "one section" during prosecution. The doctrine of prosecution disclaimer precludes patentees from recapturing through claim interpretation specific meanings disclaimed during prosecution.
As an initial matter, Genet testified that he was "not involved . . . in patent prosecution work" on the `583 patent and that he would "not have any personal knowledge outside of what was actually filed on behalf of Hollister by the previous attorneys of record." (Tr. II, 148:7-17). As such, the Court accords his testimony regarding the patent prosecution history considerably less weight than his opinions regarding literal infringement of the `583 patent. While von Dyck succeeded in eliciting testimony from Genet that certain language appeared in the file wrapper and that the patentee indeed amended the application, the Court's review of the record reveals no "clear and unmistakable" evidence of the patentee's disavowal of one catheter section.
Moreover, on redirect examination, Genet pointed out that the inventor did not distinguish the cited prior art reference by arguing that the presence of two distinct catheter sections was the difference. (Tr. II, 202-03).
(Tr. II, 203:6-13).
Therefore, in light of the evidence, the Court does not find prosecution disclaimer.
Accordingly, having rejected von Dyck's arguments, the Court concludes that Hollister has proven that the ConvaTec products literally infringe the `583 patent.
Having found infringement, the Court determines that Hollister has been damaged as a proximate result of Zassi's breach of contract and Zassi and von Dyck's misrepresentations regarding Zassi's release of patent claims against ConvaTec. The measure of damages is the amount of money that would put Hollister in as good a position as it would have been in if the Defendants had not breached the contract or made the misrepresentations and omissions at issue.
Assessing and computing damages under the patent statute, 35 U.S.C. § 284, is a matter within the sound discretion of the district court.
Hollister's benchmark for a reasonable royalty is based on the Bard settlement agreement, executed after Hollister had filed a patent infringement case against Bard for infringing the `583 patent. (Tr. I, 166-67; Pl. Ex. 57). The agreement required Hollister to dismiss the case and provided Bard with a fully paid-up non-exclusive license to the `583 patent, its parent patent, the `627 patent, as well as any children of the `583 or `627 patents. (Tr. I, 167:7-10). The license also covered the patents' foreign counterparts to provide "world peace on the patent family." (Tr. I, 167-68). As part of the settlement agreement, Bard paid Hollister $6.65 million, a one-time, lump-sum, non-refundable payment. (Tr. I, 168:21-169:1). However, the method of calculating the $6.65 million payment is not specified in the agreement. The Bard agreement characterizes the $6.65 million payment as "consideration of the release set forth in Article 3.1, the license set forth in Article 3.2, and the covenant set forth in Article 3.3," but does not break out the amount allocated for the license or characterize the payment as a royalty. (Pl. Ex. 57 at 3 ¶ 2.1).
Hollister submits that it would have offered ConvaTec a license identical in scope to the Bard agreement to settle the infringement suit, with adjustments to the dollar amount based on ConvaTec's market share. (Tr. I, 170:10-25). To determine market share, Hollister obtained data from the Global Health Exchange ("GHX"), an industry organization that collects United States market data of medical device companies and reports on their sales. (Tr. I, 171-72; Pl. Ex. 58). Seamus Kavanagh, Hollister's Vice President of Business Development, testified that many health care companies subscribe to GHX and rely on GHX's market reports. (Tr. I, 29-30). The data presented at trial represented ConvaTec, Bard, and Hollister's sales in the number of BMS kits per quarter, beginning in 2007.
To calculate its reasonable royalty, Hollister used the date on which the Bard agreement was signed (June 2011 or Q2 2011) and looked at the total sales in the marketplace in that quarter. (Tr. I, 175-76; Pl. Ex. 60). The total kits sold in Q2 2011 were 93,400 units, ConvaTec's total kits sold were 68,984, and Bard's total kits sold were 18,034. (Tr. I, 176). By dividing ConvaTec's share by the total number of kits sold, Genet calculated that ConvaTec had a 74 percent market share. (Tr. I, 177:21). Bard's market share was 19 percent. (Tr. I, 178:2). Genet then determined that ConvaTec's market share is 3.89 times larger than Bard's by dividing ConvaTec's 74 percent market share by Bard's 19 percent market share. (Tr. I, 178:16-20). Genet calculated Hollister's damages by multiplying the amount Bard paid Hollister in the Bard agreement ($6.65 million) times ConvaTec's market share (3.89) to arrive at a reasonable royalty of $25,868,500. (Tr. I, 178:21-25). Hollister also seeks $5,756,449.98 in prejudgment interest for a total damages award of $31,624,949.98, plus postjudgment interest and costs.
To justify this calculation as a reasonable royalty, Genet explained that the existence of the Bard agreement presented a "unique situation" in which to calculate Hollister's damages. (Tr. I, 180:20). Although comparable licenses offered as evidence of patent damages typically contain "all kinds of variables," such as "differences between the license[d] technology and what the parties are providing and the scope in terms of the license," Genet opined that this case is "unique" because the marketplace consists of only three competitors selling very similar products. (Tr. I, 180:19-181:24). According to Genet, the terms that Hollister would have offered to ConvaTec are exactly the same terms that were offered to Bard, including identical patents. (Tr. I, 181:6-18). Moreover, the Bard agreement contains the only license that Hollister has for its patents. (Tr. I, 183:11-12).
The Bard agreement, the numerical extrapolations from GHX data, and Genet's testimony constitute the only evidence of a reasonable royalty offered by Hollister. Von Dyck did not (nor was he required to) retain his own damages expert or provide an alternative method for calculating damages.
In its Post-Trial Proposed Findings of Fact and Conclusions of Law, Hollister characterizes the benchmark it used for its calculation of a reasonable royalty for ConvaTec as an "established royalty" insomuch as it is based on Hollister's settlement with Bard. (Doc. 186 at 14).
A reasonable royalty is the floor below which patent damages shall not fall.
A hypothetical negotiation can result in either a lump-sum license or a running royalty license.
In determining the reasonable royalty that would have been agreed to at the hypothetical negotiation, parties in patent cases frequently utilize the fifteen factors enunciated in
"Keeping in mind that section 284 commands that damages should be no less than a reasonable royalty, the Court notes that the Federal Circuit has held that a reasonable royalty `may be based upon an established royalty, if there is one, or if not upon a hypothetical royalty resulting from arm's length negotiations between a willing licensor and a willing licensee.'"
If an established royalty is found, it is generally deemed the best measure of damages for infringement.
To the extent that Hollister offers the Bard agreement as proof of an established royalty, it does not meet at least two of the criteria outlined in
Nevertheless, the Court will consider whether, in relying solely on the Bard agreement, Hollister has provided sufficient evidence of a reasonable royalty under the
"[L]icenses relied on by the patentee in proving damages [must be] sufficiently comparable to the hypothetical license at issue in suit."
Nevertheless, Hollister argues that the Bard agreement is the best, most comparable, most reliable evidence because it is the only license to the patent in suit. The Bard agreement is purportedly identical in every way to what Hollister would have offered ConvaTec to settle its infringement suit: it concerns the same patent, its family, and its foreign counterparts. It constitutes a one-time, lump-sum payment for a fully paid-up, non-exclusive worldwide license. Moreover, Hollister, Bard, and ConvaTec are the only three competitors in the relevant market. This leads Hollister to argue in its post-trial reply that "Hollister's license to Bard necessarily must be deemed sufficient evidence because it is the
To support this position, Genet testified that because the Bard agreement was a settlement license, that made it an even
While this argument has initial appeal, the Bard agreement has a glaring flaw as a comparator: its settlement amount of $6.65 million exists in a vacuum. In
The Bard agreement's base number of $6.65 million represents the type of "fundamentally flawed premise" that the Federal Circuit cautioned against in
(Tr. II, 70:23-71:12) (emphasis added).
(Tr. II, 72:13-74:7) (emphasis added).
(Tr. II, 92:9-22).
(Tr. II, 242:2-12) (emphasis added).
At the conclusion of Genet's testimony, the undersigned expressed concern that Genet had "no idea" why Bard settled for $6.65 million, noting that "people settle for all kinds of reasons for all kinds of amounts" and that "$6.65 million, there's nothing sacrosanct about it." (Tr. II, 242:19-243:3).
(Tr. II, 243:21-244:5). Of course, this did not answer the Court's question as to why the $6.65 million represented a reasonable royalty.
The Court is mindful of the Federal Circuit's rejection of lump-sum licenses in
Hollister could have provided the Court with key information required to evaluate the Bard agreement as a benchmark of a reasonable royalty. See In re MSTG, Inc., 675 F.3d 1337, 1348 (Fed. Cir. 2012) (holding that settlement negotiations related to reasonable royalties and damage calculations are not protected by a settlement negotiation privilege and thus the district judge did not abuse his discretion by ordering the production of negotiation documents underlying settlement agreements). While the Bard agreement itself does not address the royalty issue, see supra Part III.A, as one of only two parties to the Bard agreement, Hollister presumably had this information at its disposal and could have asked Bard to consent to its use in this lawsuit or, if necessary, asked the Court to allow its disclosure. At the very least, Hollister could have called its own legal or corporate representative who negotiated the Bard settlement to testify and explain, even in non-privileged terms, the considerations that went into the final settlement number.
Courts cannot award patent damages without supporting evidence or on the basis of speculation or conjecture.
Given no other tools to arrive at a reasonable royalty, the Court cannot invent one out of thin air, particularly given that the Federal Circuit requires "sound economic proof of the nature of the market and likely outcomes" in order "to prevent the hypothetical from lapsing into pure speculation[.]"
Accordingly, it is hereby
1. To the extent consistent with the Jury Verdict and these Findings of Fact and Conclusions of Law, the Court
2. The Court will enter final judgment consistent with the Jury Verdict and these Findings of Fact and Conclusions of Law.
3. The Clerk shall then terminate all pending motions and close the file.
In 2001, ConvaTec and Zassi executed a Supply Agreement pertaining to the manufacturing and supply of products consistent with their Development and License Agreement. Disagreements arose between ConvaTec and Zassi, and in late 2005, they resolved their disputes and executed a settlement agreement. That agreement contained a provision at paragraph 10 in which Zassi forever released ConvaTec from any past, present, or future claims, including claims for patent infringement, related to ConvaTec's FMS design, marketed as the Flexi-Seal FMS product. (Pl. Ex. 6).
(Pl. Ex. 54).
Von Dyck mistakenly had the `627 file wrapper on the projector and substituted the `583 file wrapper after realizing the error. Regardless, Hollister correctly notes that von Dyck never provided Hollister, or the Court for that matter, a copy of the file wrappers, and he never formally offered either file wrapper as evidence. (Doc. 175). As a result, the Court only has Genet's cross-examination testimony to consider in evaluating the strength of von Dyck's prosecution argument.
As Hollister suggested at trial and in several of its briefs, although the Court gave von Dyck significant leeway at the damages trial to present these arguments, they were more appropriate for the liability phase and cannot now serve to reduce or eliminate Hollister's damages. Moreover, even if these arguments were properly before the Court, von Dyck has provided no basis for the Court to apply them to the damages calculation. Instead, he merely suggests that these theories demonstrate that Hollister has not sufficiently proven its damages. (Tr. II, 107). Because the Court does not rely on these arguments in analyzing Hollister's damages request, it need not address them.
Hollister's suit against Bard is distinguishable from
Hollister argues that "other benchmarks . . . support such an award including the . . . $5.9 million that ConvaTec paid to Zassi for a license and a full release of any future claims related to the BMS technology that resulted in the `583 patent. (Pl. Ex. 6)." (Doc. 196 at 8 n.5). Additionally, Hollister contends that "although [the Houlihan Lokey report was] not admitted into evidence, Defendant [von Dyck] elicited testimony from Genet that Hollister's investment brokers had valued the acquired Zassi intellectual property at $8.7 million. (Tr. II, 68:16-25)." (Doc. 196 at 8 n.5).
Neither at trial nor in its post-trial papers does Hollister seek either the $5.9 million or $8.7 million figure as its damages or explain how they relate to its $6.65 million alternative request. In fact, Genet testified that the information contained in the Houlihan Lokey report was irrelevant to the analysis of Hollister's hypothetical royalty. The report was a valuation done by outside investment brokers in June 2007 to value the intellectual property assets Hollister acquired from Zassi for tax purposes. (Tr. II, 60-61). The brokers assigned a fair value of $8.7 million to the technology. (Tr. II, 68:18-19). Genet explained that the report "was based on the current sales of Zassi and projected sales of Zassi of its product." (Tr. II, 63:4-11). "[W]hen you calculate that reasonable royalty, you're looking at the sales of the infringers." (Tr. II, 63:1-3). The "reasonable royalty analysis has nothing to do with Zassi's product or Hollister's product. It has everything to do with the ConvaTec product. So for that reason—those two reasons [different time periods and products], I think that's why this report isn't relevant or useful in a reasonable royalty analysis." (Tr. II, 63:6-11). Based on this evidence, the Court disagrees that $8.7 million represents a benchmark supporting an award of $6.65 million. Likewise, Hollister has not pointed to any evidence explaining why the $5.9 million amount ConvaTec paid to Zassi to settle business disputes in 2005 represents a reasonable benchmark to support the $6.65 million figure.
The Federal Circuit has instructed that the determination of a reasonable royalty must be based upon the entirety of the evidence, and courts are free to— indeed, must—reject the royalty figures proffered by the litigants where the record as a whole leads the court to a different figure.