United States v. Universal Management Services, Inc., Corporation Natural Choice, Inc. Corporation, Doing Business as Natural Choice Products, Inc. Paul M. Monea, Individual Paul A. Monea

191 F.3d 750, 45 Fed. R. Serv. 3d 676, 1999 U.S. App. LEXIS 21935
CourtCourt of Appeals for the Sixth Circuit
DecidedSeptember 13, 1999
Docket98-3310
StatusPublished
Cited by24 cases

This text of 191 F.3d 750 (United States v. Universal Management Services, Inc., Corporation Natural Choice, Inc. Corporation, Doing Business as Natural Choice Products, Inc. Paul M. Monea, Individual Paul A. Monea) is published on Counsel Stack Legal Research, covering Court of Appeals for the Sixth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. Universal Management Services, Inc., Corporation Natural Choice, Inc. Corporation, Doing Business as Natural Choice Products, Inc. Paul M. Monea, Individual Paul A. Monea, 191 F.3d 750, 45 Fed. R. Serv. 3d 676, 1999 U.S. App. LEXIS 21935 (6th Cir. 1999).

Opinion

191 F.3d 750 (6th Cir. 1999)

United States of America, Plaintiff-Appellee,
v.
Universal Management Services, Inc., Corporation; Natural Choice, Inc. Corporation, doing business as Natural Choice Products, Inc.; Paul M. Monea, individual; Paul A. Monea, Defendants-Appellants.

No. 98-3310

UNITED STATES COURT OF APPEALS FOR THE SIXTH CIRCUIT

Argued: August 10, 1999
Decided and Filed: September 13, 1999

Appeal from the United States District Court for the Northern District of Ohio at Cleveland; No. 95-02768--Solomon Oliver, Jr., District Judge.[Copyrighted Material Omitted][Copyrighted Material Omitted]

Cassandra P. McGurk, OFFICE OF GENERAL COUNSEL, FOOD & DRUG ADMINISTRATION, Rockville, Maryland, Alexander A. Rokakis, OFFICE OF THE U.S. ATTORNEY, Cleveland, Ohio, Deborah M. Autor, U.S. DEPARTMENT OF JUSTICE, CIVIL DIVISION, OFFICE OF CONSUMER LITIGATION, Washington, D.C., Appellee.

Michael S. Pasano, Christopher S. Carver, ZUCKERMAN, SPAEDER, TAYLOR & EVANS, Miami, Florida, for Appellants.

Before: NORRIS and SUHRHEINRICH, Circuit Judges; RICE, District Judge*.

OPINION

SUHRHEINRICH, Circuit Judge.

Defendants appeal summary judgment for plaintiff and a permanent injunction from the manufacture and sale of a device intended to relieve certain types of physical pain when applied to accupressure points. We AFFIRM.

The court of appeals reviews an order granting summary judgment de novo, and hence uses the same test as used in the district court. See Terry Barr Sales Agency, Inc. v. All-Lock Co., 96 F.3d 174, 178 (6th Cir. 1996). Summary judgment is proper "if the pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any, show that there is no genuine issue as to any material fact and that the moving party is entitled to a judgment as a matter of law." Fed. R. Civ. P. 56(c).

I.

Appellants Universal Management Services, Inc., and Natural Choice, Inc. are Ohio corporations which are managed by Appellants Paul M. Monea and his son, Paul A. Monea. As part of their business, Appellants sell and distribute a product known as the Stimulator, and also a product that connects to the Stimulator known as the Xtender. The Stimulator is essentially an electric gas grill igniter, marketed as a pain relieving device. To produce the Stimulator, Appellants purchase gas grill igniters and outfit them with finger grips. A user then places the tip of the Stimulator on his body, presses with his thumb on a plunger, and an electric current passes into that part of the body. Appellants' advertising literature states that, when applied to certain acupressure points, the Stimulator can relieve numerous kinds of pain (e.g., migraine headaches, swollen joints, allergies). J.A. at 76-77, 505, 808, 810, 814. The Xtender is an accessory that allows an individual to use the Stimulator to reach areas of the body otherwise difficult to reach, such as the spine. In total, Appellants sold a total of 800,000 gas grill ignitors, at a cost to the company of one dollar each, for $88.30 each. J.A. at 505, 793, 839.

In May 1995, U.S. Marshals seized over $1.2 million worth of Appellants' devices pursuant to seizure authority under the Federal Food, Drug & Cosmetic Act, 21 U.S.C. § 301 et seq. (FDCA). J.A. at 782-84. Later that month, the Food and Drug Administration (FDA) informed Appellants that they considered the devices adulterated and subject to regulation, threatening further legal action if approval was not sought and distribution did not cease. J.A. at 78. Distribution did not cease and the Government sought the injunction that is the subject of this appeal. The district court granted summary judgment for the Government on December 30, 1997, and, in February 1998, rejected Appellants' Motion for Reconsideration. J.A. at 774-75. The resulting judgment placed a permanent injunction against the distribution of Appellants' products and ordered Appellants to offer full refunds to all customers who had purchased their devices after the May 1995 seizure. J.A. at 39, 50.

II.

The district court concluded that the Stimulator and Xtender are "adulterated" devices under the FDCA. Specifically, the Government claims that Appellants violated 21 U.S.C. § 331(a) and § 331(k), which prohibit misbranding or adulterating medical devices and introducing such devices into interstate commerce.

To show a violation of §§ 331(a) and (k), the Government must prove: (1) Appellants' products are "devices" within the meaning of the FDCA; (2) the devices are adulterated or misbranded; and (3) the devices move in interstate commerce. The third element is undisputed.

A device is "adulterated" under the FDCA if it is required to receive premarket approval ("PMA") from the FDA but moves in commerce even though it did not receive this PMA. See 21 U.S.C. § 351(f)(1)(B); United States v. An Article of Device Consisting of 1,217 Cardboard Boxes, 607 F.Supp. 990, 998 (W.D. Mich. 1985). Whether a device is required to receive a PMA from the FDA depends on a scheme set out in 21 U.S.C. § 360c. Under this scheme, all medical devices are categorized as Class I (minimal regulation), Class II (intermediate regulation), or Class III (stringent regulation) devices. All "new devices," those not on the market before 1976, are, as a default, automatically Class III devices.

Class III devices cannot be marketed unless either: (1) the manufacturer has submitted to the FDA an application for a PMA and receives approval; or (2) the manufacturer submits a "premarket notification" arguing that its device should be reclassified as Class I or II because it is substantially equivalent to an existing device so categorized and the FDA finds the devices are in fact so equivalent.

Appellants contend that their products1 are not violative of §§ 331(a) & (k) for three reasons. First, they argue their products are not devices within the meaning of the FDCA. The FDCA's definition of "device" is as follows:

The term "device" . . . means an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including any component, part or accessory, which is . . .

(2) intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals, or

(3) intending to affect the structure or any function of the body of man or other animals, and

which does not achieve its primary intended purpose through chemical action within or on the body of man or other animals and which is not dependent upon being metabolized for the achievement of its primary intended purposes.

21 U.S.C. § 321(h).

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Bluebook (online)
191 F.3d 750, 45 Fed. R. Serv. 3d 676, 1999 U.S. App. LEXIS 21935, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-v-universal-management-services-inc-corporation-natural-ca6-1999.