Silverwing Medical LLC v. Adorama Inc. and Kitchen Winners NY Inc.

CourtDistrict Court, E.D. New York
DecidedNovember 25, 2025
Docket1:21-cv-04082
StatusUnknown

This text of Silverwing Medical LLC v. Adorama Inc. and Kitchen Winners NY Inc. (Silverwing Medical LLC v. Adorama Inc. and Kitchen Winners NY Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Silverwing Medical LLC v. Adorama Inc. and Kitchen Winners NY Inc., (E.D.N.Y. 2025).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK

SILVERWING MEDICAL LLC,

Plaintiff, v. MEMORANDUM AND ORDER

ADORAMA INC. and KITCHEN WINNERS NY 21-CV-4082 (LDH) (JAM) INC.,

Defendants.

LASHANN DEARCY HALL, United States District Judge: Silverwing Medical LLC (“Silverwing” or “Plaintiff”) brings the instant action asserting claims against Adorama, Inc. (“Adorama”) and Kitchen Winners NY, Inc. (“Kitchen Winners”) (together, “Defendants”) for fraud, breach of contract, and unjust enrichment. Defendants assert a counterclaim against Plaintiff for breach of contract. Plaintiff moves, pursuant to Rule 56 of the Federal Rules of Civil Procedure, for summary judgment on its breach of contract and fraud claims. Defendants move, pursuant to Rule 56 of the Federal Rules of Civil Procedure, for summary judgment on Plaintiff’s breach of contract, unjust enrichment, and fraud claims, as well as summary judgment on its counterclaim for breach of contract. UNDISPUTED FACTS1 In February 2021, Plaintiff and Defendants entered into a Sales and Purchase Agreement (the “SPA”), pursuant to which Defendants agreed to sell Plaintiff one million boxes of nitrile gloves at a total purchase price of $10.5 million. (Defs.’ Resp. 56.1 Statement ¶ 1, ECF No. 52-

1 The following facts are undisputed unless otherwise noted. Further, facts that were not contradicted by citations to admissible evidence are deemed admitted. See Giannullo v. City of New York, 322 F.3d 139, 140 (2d Cir. 2003) (“If the opposing party . . . fails to controvert a fact so set forth in the moving party’s Rule 56.1 statement, that fact will be deemed admitted.”). 1; Decl. of Elliot Hahn (“Hahn Decl.”), Ex. 1, Sales and Purchase Agreement (“SPA”) § 1, ECF No. 50-6.) Specifically, the SPA provides for the sale of one million 100-count boxes of “LevMed” brand blue nitrile gloves that are “[m]edical exam grade with FDA 510k [certification],”2 in an assortment of sizes, at a unit price of $10.50 per box. (SPA § 1.) Prior to

the execution of the SPA, Defendants sent Plaintiff product samples. (Defs.’ Resp. 56.1 Statement ¶ 5.) The parties dispute whether the product samples that were sent to Plaintiff were accompanied by documentation indicating that the company manufacturing the product, and the holder of the FDA 510(k) certification, was called Zhangjiang Jiali Glove Products Co., Ltd. (Id.; see also Hahn Decl., Ex. 4 (“Jiali Glove Prod. Spec.”), ECF No. 50-9.) At the time the SPA was executed, Plaintiff paid Defendants a $1.05 million deposit. (Defs.’ Resp. 56.1 Statement ¶ 6, SPA § 2(a).) The remaining 90% of the purchase price “for each shipment of goods” was to be paid to Defendants within 48 hours of delivery of a trackable bill of lading for the shipment to Plaintiff. (SPA § 2(c).) The SPA includes a “manufacturing disclaimer,” stating that Defendants are merely resellers and that they make no warranties about the products “except that they

conform to the specifications provided.” (Id. § 5.) The agreement further provides that, “[i]n the event that upon arrival of the [p]roducts to the destination port, [Plaintiff]’s inspection reveals that the [p]roducts are not in conformance with the SGS report provided by [Defendants], [Plaintiff] shall be entitled to the full refund of the purchase price paid for the [p]roducts delivered.” (Id. § 7.)

2 The Food and Drug Administration (“FDA”) requires companies manufacturing and importing medical devices for commercial distribution to register and submit listing information for those devices with the FDA. See generally 21 C.F.R. § 807. Companies that are required to register under this provision must also submit a “premarket notification submission” to the FDA, which includes, among other things, a “510(k) summary” or “510(k) statement” providing the basis for a determination by the FDA that the product is “substantially equivalent” to an already-approved device in commercial distribution. Id. §§ 807.81, .92, .93. Upon review of the 510(k) submissions, the FDA issues a determination of substantial equivalence. Id. § 807.92. The gloves purchased by Plaintiff were to have the requisite 510(k) certification from the FDA. (See SPA § 1.) On March 24, 2021, upon receipt of bills of lading, (see Defs.’ Resp. 56.1 ¶ 11), Plaintiff sent an additional $265,545 to Defendants, (see id. ¶ 9). Instead of providing Plaintiff with an “SGS report,” however, Defendants provided Plaintiff with a pre-shipment inspection report from V-Trust Inspection Service, dated March 25, 2021 (the “V-Trust Report”). (Id. ¶¶ 10-11;

Hahn Decl., Ex. 6 (“V-Trust Report”), ECF No. 50-11.) The V-Trust Report did not identify the factory where the gloves were made, and listed both the “client” and “supplier” of the product as “Kitchen Winners Inc.” (Defs.’ Resp. 56.1 Statement ¶¶ 14-15; V-Trust Report at 1.) The report also stated that it was in a “Custom-made report format for GTS Limited for [m]edical gloves,” (V-Trust Report at 16), and contained pictures of gloves that listed the name Qingdao Zhongyang Medical Equipment Co., Ltd. (“Qingdao”), (id.; Defs.’ Resp. 56.1 Statement ¶ 17). The report listed an order quantity of fifteen million gloves. (Defs.’ Resp. 56.1 Statement ¶ 16; V-Trust Report at 7.) The parties dispute whether the V-Trust Report was altered from the version of the report that V-Trust Inspection Service maintained in its files. (Defs.’ Resp. 56.1 Statement ¶ 33.)

Plaintiff expressed concerns about the identity of the manufacturer of the gloves and the manufacturer’s FDA 510(k) certification. (See Defs.’ Resp. 56.1 Statement ¶ 22.) On March 30, 2021, to address Plaintiff’s concerns, Defendants sent Plaintiff a copy of an FDA 510(k) certification letter from a company named Zhonghong Pulin Medical Products Co., LLC (“Pulin”), dated March 9, 2016. (Defs.’ Resp. 56.1 Statement ¶¶ 22-23.) The parties do not dispute that Pulin has a valid 510(k) certification in connection with the manufacturing of medical gloves. (Pl.’s Resp. 56.1 Statement ¶ 20, ECF No. 58-1.) The parties dispute whether, on March 30, 2021, Defendants sent Plaintiff a letter written on the letterhead of a company called “ZhongHong Pulon Medical Products Co., Ltd.,” rather than Pulin, stating: “This letter is to confirm [w]e [m]anufacture the Levmed Brand under our secondary factory named: Qingdao Zhongyang Medical Equipment Co., LTD Which is being manufactured all under our 510K # K152712 [sic].” (Defs.’ Resp. 56.1 Statement ¶ 25.) Defendants made representations to Plaintiff that the gloves Plaintiff received from Qingdao were manufactured by Pulin. (See

Defs.’ Resp. 56.1 Statement ¶ 25; Pl.’s Resp. 56.1 Statement ¶ 11, ECF No. 54-1.) The parties dispute whether Qingdao has any affiliation with Pulin, and whether Pulin manufactures any Levmed products. (Defs.’ Reply 56.1 Statement ¶¶ 24-25, ECF No. 60-1.) Plaintiff made additional payments to Defendants of $400,000 and $450,000 between April 8, 2021 and April 9, 2021. (See Defs.’ Resp. 56.1 Statement ¶ 32; Hanh Decl., Ex. 5 at 4, ECF No. 50-10.) In April 2021, a broker acting on behalf of Plaintiff, Eli Marciano (“Mr. Marciano”), went to a California warehouse that purportedly held a portion of the product delivered by Defendants pursuant to the SPA. (Def.’s Resp.

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Bluebook (online)
Silverwing Medical LLC v. Adorama Inc. and Kitchen Winners NY Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/silverwing-medical-llc-v-adorama-inc-and-kitchen-winners-ny-inc-nyed-2025.