United States v. Nutri-Cology, Inc., D/B/A Allergy Research Group Biocurrents, Inc. Stephen A. Levine Susan D. Levine

982 F.2d 394, 92 Daily Journal DAR 17503, 92 Cal. Daily Op. Serv. 10384, 1992 U.S. App. LEXIS 33629, 1992 WL 382903
CourtCourt of Appeals for the Ninth Circuit
DecidedDecember 29, 1992
Docket91-16419
StatusPublished
Cited by137 cases

This text of 982 F.2d 394 (United States v. Nutri-Cology, Inc., D/B/A Allergy Research Group Biocurrents, Inc. Stephen A. Levine Susan D. Levine) is published on Counsel Stack Legal Research, covering Court of Appeals for the Ninth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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United States v. Nutri-Cology, Inc., D/B/A Allergy Research Group Biocurrents, Inc. Stephen A. Levine Susan D. Levine, 982 F.2d 394, 92 Daily Journal DAR 17503, 92 Cal. Daily Op. Serv. 10384, 1992 U.S. App. LEXIS 33629, 1992 WL 382903 (9th Cir. 1992).

Opinion

PREGERSON, Circuit Judge:

The government appeals the district court’s denial of its motion for a preliminary injunction and its motion for reconsideration. The government sought to enjoin appellees Nutri-cology, Inc., also doing business as Allergy Research Group, Bio-currents, Inc., Stephen A. Levine, and Susan D. Levine (collectively “Nutri-cology”) from distributing certain products, which the government contends are unapproved “drugs” or “new drugs” within the meaning of the Food, Drug and Cosmetic Act (the “FDCA”), 21 U.S.C. §§ 301-394. The district court found that the government had made a colorable showing that the products were unapproved “new drugs” and were being distributed in violation of 21 U.S.C. § 331(d). Nonetheless, the dis *396 trict court found that the government failed to demonstrate irreparable harm and refused to issue a preliminary injunction. We have jurisdiction under 28 U.S.C. § 1292(a)(1), and we affirm.

I. BACKGROUND

Nutri-cology distributes and promotes a number of products labelled as nutritional or dietary supplements. These products are allegedly promoted as useful to prevent and treat numerous diseases and conditions.

The Food and Drug Administration (the “FDA”) began monitoring Nutri-cology’s activities in 1982. The FDA notified defendants in writing — three times in 1982, twice in 1985, and twice in 1988 — that the FDA considered Nutri-cology’s products to be unapproved “drugs” and “new drugs” under the FDCA. The FDA also held two meetings with Nutri-cology’s counsel, in 1982 and 1988, where the alleged violations of the FDCA were reiterated.

Since 1982, Nutri-cology has maintained that its products are not “drugs” or “new drugs,” under the FDCA, but are herbs, oils, vitamins, and other “foods.” The FDA sent its last communication to Nutricology on June 16, 1988. The government filed this action three years later on May 2, 1991.

On May 8, 1991, the district court granted the government’s ex parte request for a temporary restraining order enjoining Nutri-cology from further marketing nine of its products, which constituted 80% of Nutri-cology’s business.

On May 23, 1991, the district court denied the government’s motion for a preliminary injunction. The district court applied the following preliminary injunction standard: “ ‘the moving party must show either (1) a combination of probable success on the merits and the possibility of irreparable harm, or (2) that serious questions are raised and the balance of hardships tips sharply in the moving party’s favor.’ ” May 23, 1991 Order at 5 (quoting Rodeo Collection, Ltd. v. West Seventh, 812 F.2d 1215, 1217 (9th Cir.1987)).

The district court made the following findings: (1) the government made a threshold evidentiary showing that Nutricology intended its products to be perceived as beneficial in preventing or treating diseases; (2) the government created some showing that Nutri-cology’s products were “drugs” falling under the auspices of 21 U.S.C. § 321(g)(1)(B); and (3) the government made a colorable showing that Nutricology was violating 21 U.S.C. § 331(d) by marketing unapproved “new drugs.” The court further concluded that a rebuttable presumption of irreparable harm arose from the colorable showing of an FDCA violation.

The district court then concluded that the presumption of irreparable harm was rebutted by Nutri-cology’s extensive showing, through the petition signed by sixty physicians and nutritionists, in support of the merit and reliability of its products. Nutri-cology’s showing was particularly persuasive because the government failed to demonstrate any harm to consumers. The district court found that two other factors weighed against granting the preliminary injunction: the FDA’s nine-year delay in bringing the action, and the likelihood that an injunction would destroy Nutri-cology’s business.

On July 19, 1991, the district court denied the government’s motion for reconsideration. On September 10, 1991, the government filed its notice of appeal.

II. TIMELINESS OF APPEAL

Under Fed.R.App.P. 4(a)(1), in a matter where the United States is a party, a notice of appeal must be filed within sixty days after the date of the order which is being appealed. The order appealed from in this case is the district court’s denial of the preliminary injunction on May 23, 1991. Therefore, unless the time for filing the notice of appeal was tolled, the government was required to file its notice by July 22, 1991. Under Fed.R.App.P. 4(a)(4), certain motions made under Fed.R.Civ.P. 50(b), 52(b), and 59 toll the deadline for filing the notice of appeal. In connection with such motions, where the United States is a par *397 ty, a notice of appeal must be filed within sixty days of the order disposing of the motion.

The government did not cite the rule that authorized its motion for reconsideration. The district court treated the government’s motion as being brought under Fed.R.Civ.P. 60(b); motions made under Rule 60(b) do not toll the time for filing a notice of appeal. The government’s motion for reconsideration, however, could have been brought under Fed.R.Civ.P. 59(e)— motion to alter or amend a judgment. A motion, however labelled, served within ten days of the entry of an order that could have been brought under Rule 59(e) tolls the time for filing a notice of appeal. Sierra On-Line, Inc. v. Phoenix Software, Inc., 739 F.2d 1415, 1419 (9th Cir.1984). The government’s notice of appeal, filed within sixty days of the order denying its motion for reconsideration, was therefore timely.

III. STANDARD OF REVIEW

A district court’s order regarding preliminary injunctive relief is subject to limited review. The denial of a preliminary injunction will be reversed only where the district court abused its discretion or based its decision on an erroneous legal standard or on clearly erroneous findings of fact. Senate of Cal. v. Mosbacher, 968 F.2d 974, 975 (9th Cir.1992); Religion Technology Center, Church of Scientology Int’l, Inc. v. Scott,

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982 F.2d 394, 92 Daily Journal DAR 17503, 92 Cal. Daily Op. Serv. 10384, 1992 U.S. App. LEXIS 33629, 1992 WL 382903, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-v-nutri-cology-inc-dba-allergy-research-group-ca9-1992.