The Janz Corporation v. Philips North America LLC

CourtDistrict Court, D. Massachusetts
DecidedFebruary 12, 2024
Docket1:23-cv-11025
StatusUnknown

This text of The Janz Corporation v. Philips North America LLC (The Janz Corporation v. Philips North America LLC) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
The Janz Corporation v. Philips North America LLC, (D. Mass. 2024).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MASSACHUSETTS

_______________________________________ ) THE JANZ CORPORATION, ) ) Civil Action No. Plaintiff, ) 23-11025-FDS ) v. ) ) PHILIPS NORTH AMERICA LLC d/b/a ) PHILIPS HEALTHCARE, a subsidiary of ) KONINKLIJKE PHILIPS N.V., ) ) Defendant. ) _______________________________________)

MEMORANDUM AND ORDER ON DEFENDANT’S MOTION TO DISMISS SAYLOR, C.J. This is an action arising out of the termination of a contract between The Janz Corporation and Philips North America. The complaint alleges that Philips breached the implied covenant of good faith and fair dealing by terminating the agreement in retaliation for Janz’s repeated raising of government product-certification concerns. It alleges further that the termination violated Massachusetts public policy and Mass. Gen. Laws ch. 93A. Jurisdiction is based on diversity of citizenship. Defendant has moved to dismiss the complaint pursuant to Fed. R. Civ. P. 12(b)(6) for failure to state a claim upon which relief can be granted. For the reasons set forth below, the motion to dismiss will be granted in part and denied in part. I. Background The facts are set forth as alleged in the complaint unless otherwise noted. A. Factual Background The Janz Corporation is a service-disabled veteran-owned small business that provides medical equipment and services to certain federal government agencies. (Compl. ¶ 9). It is organized under the laws of Michigan, and its principal place of business is Columbus, Ohio. (Id.).

Philips North America LLC d/b/a Philips Healthcare is a limited liability company that is wholly owned by Koninklijke Philips N.V., a Dutch corporate entity. (Corp. Disclosure, ECF No. 11). In February 2014, Janz and Philips entered into a reseller agreement. (Id. ¶ 18). Under the agreement, Janz was authorized to promote, sell, and support certain Philips products, including the IntelliVue MP2 Mobile Patient Monitor (“MP2”). (Id. ¶¶ 15, 18). The MP2 is a portable medical-monitoring device regularly used on commercial and government aircraft. (Id. ¶ 15). For use on government aircraft, such devices must be certified for airworthiness, which requires government-sanctioned review, testing, and approval of all MP2 component parts to ensure that they (1) will work in the air, (2) will not obstruct the

operation of the aircraft, and (3) will not enable hostile detection. (Id. ¶ 16). The complaint alleges that the agreement was renewable annually and was renewed each year from 2015 to 2018. (Id. ¶ 19).1 The agreement provided that either party “may terminate this Agreement . . . without cause at any time upon thirty (30) days prior written notice to the other Party.” (Id. ¶ 18). In late 2014, Philips notified Janz it was modifying the MP2. The modification would

1 The parties dispute whether there were a series of one-year term contracts or a renewed contract. (Mem. at 3 n.3). For present purposes, the distinction is not relevant. mean that the MP2 was no longer certified airworthy for government customers. (Id. ¶ 21). In response, Janz asked Philips about recertification and airworthiness. In subsequent months, the parties exchanged communications about recertification and airworthiness, including an e-mail on February 6, 2015, in which a Philips senior marketing manager stated it was unclear if the

MP2 sales would justify the expense of re-testing. (Id. ¶¶ 22-27). In June 2015, Janz received an order from the Army 18th Airborne Corps at Fort Bragg, North Carolina, for 42 certified MP2s. (Id. ¶ 28). Philips allegedly agreed to fill the order with airworthy-certified MP2s only if Janz agreed to accept an additional 90 airworthy-certified MP2s. Janz accepted. (Id.). On July 7, 2015, Philips allegedly acknowledged that it was struggling to stock orders on time because of the requirements for producing airworthy MP2s. (Id. ¶ 29). On July 8, 2015, Philips informed Janz it would sell airworthy-certified MP2s in a “bundle” that would be available in October 2015 to satisfy Janz’s contract with its government customer. (Id. ¶ 31). On August 4, 2015, Janz entered into a five-year agreement with the government to

provide approved Philips products, including MP2s. (Id. ¶ 20). On September 18, 2015, Janz sold four MP2s to a United States Coast Guard unit in Atlantic City, New Jersey. (Id. ¶ 36). According to the complaint, a Philips employee traveled on site to configure the MP2s for the Coast Guard’s use and discovered that the MP2s provided by Philips were the remodeled devices that lacked airworthiness certification. The Philips employee also suggested that it was likely that Janz’s order for the 18th Airborne included uncertified MP2s. (Id.). On November 20, 2015, Janz e-mailed a senior manager of Philips to condition the purchase order for the 18th Airborne order on confirmation of additional time to pay for the 90 units, the option to return part or all of the units without penalty, and an assurance that Philips would only supply airworthy-certified MP2s. (Id. ¶ 37). The manager responded, in part, “[D]on’t get caught short not having enough of these units to fulfill [the] order when they do happen. Mind you no other reseller will know about the airworthy ones.” (Id. ¶ 38).

According to the complaint, a Philips interoffice memorandum confirmed that Philips had been supplying orders from government customers with MP2s that were not certified for airworthiness. (Id. ¶ 39). The memorandum stated that Philips had developed a “new 6N Number 867059/M8102AM for the Intellivue MP2 Military version” that was different from the “currently shipping MP2 and MP2 Military version which is based on a HW revision that includes the previous main board and power board revision (Military tested version).” (Id.). On August 4, 2017, Janz asked for confirmation whether the MP2M was certified as airworthy, noting that the Navy had expressed skepticism of its certification status after discovering previously purchased MP2s may not have been certified. (Id. ¶ 41).2 According to the complaint, Philips did not respond. (Id.).

On August 14, 2017, Philips contracted with Janz to certify the Lumify Ultrasound product as airworthy, which Janz accomplished. (Id. ¶ 55). The complaint alleges Philips had previously provided Janz a “Letter of Supply” for a High Tech Medical Equipment contract with government customers, under which Philips would supply ultrasound products, including the Lumify, for five years. Janz became the stocking distributor for Lumify products. (Id.). Janz also worked with the Air Force to retest the MP2M for airworthiness. On September 26, 2018, the MP2M was certified airworthy. (Id. ¶ 42). Shortly after that certification, Philips allegedly replaced internal components of MP2M, which invalidated the

2 The MP2M appears to be the “Intellivue MP2 Military version.” (Id. ¶ 39). certification. (Id. ¶ 43). According to the complaint, Janz “confronted Philips immediately upon learning of its remodeling of the MP2M.” (Id. ¶ 44). Philips did not explain its conduct. (Id.). In October 2018, Philips notified Janz that it would no longer sell MP2 products to Janz for resale to any customer and that it would not renew the Reseller Agreement for 2019 or 2020.

(Id. ¶ 44). The complaint alleges that the termination was in retribution for Janz’s repeated insistence that MP2 products be certified as airworthy. (Id. ¶ 45). On November 30, 2018, Philips sent Janz a modification of the reseller agreement that removed patient-monitoring products from the list of products that Janz could provide to customers. (Id. ¶ 52). The complaint alleges that Janz had contracts in place for such products and when it raised that issue, Philips removed “nearly every other product” from the authorized list in response. (Id. ¶ 53).

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The Janz Corporation v. Philips North America LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/the-janz-corporation-v-philips-north-america-llc-mad-2024.