PureWick Corporation v. Sage Products, LLC

District Court, D. Delaware·Decided March 31, 2023·No. 1:22-cv-00102·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE

PUREWICK CORPORATION, ) ) Plaintiff, ) ) v. ) C.A. No. 22-102-MN ) SAGE PRODUCTS, LLC, ) ) Defendant. )

MEMORANDUM OPINION

John W. Shaw, Andrew E. Russell, SHAW KELLER LLP, Wilmington, DE; Steve C. Cherny, Raymond Nimrod, Brian P. Biddinger, Matthew A. Traupman, Nicola R. Felice, Jason C. Williams, Bianca Fox, QUINN EMANUAL URQUHART & SULLIVAN, LLP, New York, NY; Jared W. Newton, QUINN EMANUEL URQUHART & SULLIVAN, LLP, Washington, DC; John Yang, QUINN EMANUEL URQUHART & SULLIVAN, LLP, Dallas, TX – Attorneys for PureWick Corporation

Anne Shea Gaza, Samantha G. Wilson, YOUNG CONAWAY STARGATT & TAYLOR, LLP, Wilmington, DE; Robert A. Surrette, Sandra A. Frantzen, Deborah A. Laughton, Christopher M. Scharff, Ryan J. Pianetto, MCANDREWS, HELD & MALLOY, LTD., Chicago, IL – Attorneys for Sage Products, LLC

March 31, 2023 Wilmington, Delaware REJKA, U.S. DISTRICT JUDGE Presently before the Court is the motion of Plaintiff PureWick Corporation (“Plaintiff” or “PureWick”) for judgment on Defendant’s defenses of invalidity and unenforceability under Federal Rule of Civil Procedure 12(c) based on collateral estoppel. (D.I. 12). For the reasons set forth below, Plaintiff’s motion is GRANTED-IN-PART and DENIED-IN-PART. 1. BACKGROUND Plaintiff and Defendant Sage Products, LLC (“Defendant” or “Sage”) both sell products related to external vacuum-assisted urine collection. (See D.I. 1 4§ 8-13). More specifically, Plaintiff sells the PureWick FEC Solution, a female external catheter, and Defendant also sells a line of external female catheters, which are marketed under the PrimaFit name. (See id.). The external urine collection devices at issue help reduce the need for indwelling catheters and reduce the incidence of catheter-associated urinary tract infections and other moisture-related skin injuries in women. (See id. § 8). Plaintiff owns several patents related to external female catheters, two of which are relevant to the present motion: U.S. Patent Nos. 10,226,376 (“the °376 Patent”) and 10,390,989 (“the °989 Patent”). (See id. 9-10). On August 12, 2019, Plaintiff sued Defendant for patent infringement, alleging that Defendant’s original PrimaFit product (“PrimaFit 1.0”) infringed the °376 and ’989 Patents.! (See generally PureWick Corp. v. Sage Products, LLC, C.A. No. 19-1508-MN (“PureWick I’); see also PureWick I, D.1. 44). In PureWick I, Plaintiff asserted claims 1, 5 and 9 of the °376 Patent and claims 1 and 6 of the °989 Patent. Defendant filed an Answer with defenses and counterclaims of invalidity and unenforceability. (PureWick I, D.I. 53). From March 28, 2022 to April 1, 2022, the Court presided over a jury trial. (See PureWick I, D.I. 326, 327, 328, 329, 330). The jury found

Plaintiff later added two other patents not relevant to the present motion: U.S. Patent Nos. 8,287,508 and 10,376,407. (See D.I. 11 & 46).

that Defendant infringed claims 1, 5 and 9 of the ’376 Patent and claims 1 and 6 of the ’989 Patent and, further, that that infringement was willful. (See PureWick I, D.I. 316 at 2-3). The jury also found that Defendant failed to prove that any of the asserted claims is invalid. (See id. at 4). The jury awarded Plaintiff $26,215,545 in lost profits for sales of the PrimaFit 1.0 product. (Id. at 5). On April 7, 2022, the Court entered judgment on the jury verdict under Rule 58(b) of the Federal

Rules of Civil Procedure. (PureWick I, D.I. 320). Post-trial motions ensued. After dispositive motions but before trial in PureWick I, on January 26, 2022, Plaintiff filed the present action against Defendant, alleging that Defendant’s PrimaFit 2.0 infringes the ’376 and ’989 Patents.2 (D.I. 1). In this second case, Plaintiff is asserting claims 1, 5, 9 and 10 of the ’376 Patent and claims 2-7 of the ’989 Patent. (D.I. 75). On May 9, 2022, Defendant filed an Answer to the Complaint, raising a number of defenses, including that the ’376 and ’989 Patents are invalid and unenforceable. (See D.I. 8 ¶¶ 66-69, 71-84 & 90-115). Thereafter, on June 17, 2022, Plaintiff filed the instant motion under Rule 12(c) seeking judgment on Defendant’s defenses of invalidity and unenforceability of the ’376 and ’989 Patents based on collateral estoppel and res judicata.

(D.I. 12). On January 20, 2023, the Court heard oral argument, during which Plaintiff dropped its arguments that these defenses are barred based on res judicata. (See generally D.I. 123; see also id. at 4:12-20 (“[F]or purposes of this argument and in order to focus down, we’re willing to focus down and . . . leave res judicata be for the moment or forever.”))). The Court has just issued its post-trial opinion in PureWick I, finding in relevant part that substantial evidence supported the jury’s finding of no invalidity of the ’376 and ’989 Patents and, further, that Plaintiff was entitled to judgment on Defendant’s counterclaims of unenforceability and invalidity for which Defendant failed to present evidence on at trial. (See generally

2 PrimaFit 2.0 was not at issue in the original PureWick I trial. PureWick I, D.I. 368). The issue now before the Court in this second case is whether the determination of no invalidity and no unenforceability in PureWick I should apply here under the principles of collateral estoppel. II. LEGAL STANDARD Collateral estoppel (also known as issue preclusion) is a doctrine that operates to preclude

a party from relitigating an issue that has previously been decided. See Anderson v. Gen. Motors LLC, No. 18-621-LPS, 2019 WL 4393177, at *4 (D. Del. Sept. 13, 2019). Under Third Circuit law, collateral estoppel applies when: (1) the identical issue was previously adjudicated, (2) that issue was actually litigated, (3) the previous determination was necessary to the decision and (4) the party being precluded from relitigating the issue was fully represented in the prior action. See Jean Alexander Cosmetics, Inc. v. L’Oreal USA, Inc., 458 F.3d 244, 249 (3d Cir. 2006); see also Allergan, Inc. v. Sandoz, Inc., 681 F. App’x 955, 959 (Fed. Cir. 2017) (regional circuit law governs issues of collateral estoppel). The Third Circuit has also described the inquiry as looking to whether the party being precluded had a “full and fair opportunity” to litigate the contested issue in the previous action and whether that issue was decided by a “final and valid

judgment.” Jean Alexander, 458 F.3d at 249 (citations omitted). Similarly, in the patent context, the Federal Circuit has explained that “a judgment of invalidity will have no collateral estoppel effect if the patentee can show that it did not have a full and fair opportunity to litigate.” Pharmacia & Upjohn Co. v. Mylan Pharm., Inc., 170 F.3d 1373, 1379 (Fed. Cir. 1999). “The party seeking to effectuate an estoppel has the burden of demonstrating the propriety of its application.” Suppan v. Dadonna, 203 F.3d 228, 233 (3d Cir. 2000). III. DISCUSSION The Court begins with a discussion of the invalidity defenses and counterclaims decided in PureWick I before turning to the factors in the collateral-estoppel analysis. A. Invalidity and Unenforceability Defenses and Counterclaims in PureWick I In PureWick I, Defendant asserted that the patents-in-suit were invalid under § 102, § 103 and/or § 112 and that the patents were unenforceable based on several grounds. (PureWick I, D.I. 53 ¶¶ 133 & 135; see also id. at Counterclaims II & III)).

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