State Ex Rel. Miller v. New Womyn, Inc.

679 N.W.2d 593, 2004 Iowa Sup. LEXIS 156, 2004 WL 1058157
CourtSupreme Court of Iowa
DecidedMay 12, 2004
Docket02-1049
StatusPublished
Cited by7 cases

This text of 679 N.W.2d 593 (State Ex Rel. Miller v. New Womyn, Inc.) is published on Counsel Stack Legal Research, covering Supreme Court of Iowa primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
State Ex Rel. Miller v. New Womyn, Inc., 679 N.W.2d 593, 2004 Iowa Sup. LEXIS 156, 2004 WL 1058157 (iowa 2004).

Opinion

LARSON, Justice.

The State of Iowa, through its attorney general, brought an action under our Consumer Fraud Statute, Iowa Code § 714.16 (1999), against New Womyn, Inc. and its president, Dan Kaiser, based on the defendants’ promotion and sale of a breast-enlargement device called a “Stimulation VII.” Acting on a complaint filed by a New Womyn customer, the attorney general unsuccessfully sought information from the defendants about their product. The attorney general ultimately applied for, and the court granted, a default against the defendants for their failure to comply with discovery requests and related court orders. The court entered a judgment against the defendants for restitution, civil penalty, and related costs. We affirm.

I. Prior Proceedings.

New Womyn’s claims for its Stimulation VII were: it would permanently enlarge breast tissue, result in breast enlargement of two to four cup sizes, and would even regrow breasts that had been removed by mastectomy. New Womyn claimed the device had been proven to be safe and effective.

On September 21, 1999, the attorney general directed a Civil Investigative Demand (CID), under Iowa Code section 714.16(3)(a), to the defendants requesting information about the company and its customers. The defendants did not comply, and on January 11, 2000, the attorney general filed a petition under the Consumer Fraud Act. The petition asserted that the defendants had committed consumer fraud and requested an injunction pending *595 the defendants’ compliance with the pending CID.

On March 8, 2001, the district court ordered the defendants to produce customer information, including names, dates of purchase, and amounts of the customers’ payments. As of September 11, 2001, the defendants still had not complied with the request for information, and the court set a hearing for October 26 on the attorney general’s motion to compel discovery. On October 26, 2001, the court ordered the defendants to produce the customer infor? mation and to make any experts they intended to use available for deposition. The defendants tentatively identified expert witnesses but failed to provide background information on them within the time required by the court. They did not provide any customer information.

On November 13, 2001, the attorney general filed a motion for default “and/or to exclude evidence.” As of that time, the defendants had not complied with the court’s orders of March 8, 2001, and October 26, 2001, to produce the customer information. As of November 19, 2001, the date set for trial, the defendants still had not produced the information.

On the date set for trial, defendant Kaiser did not appear — either on his own behalf or on behalf of the corporation. The court asked the defendants’ attorney, Jay Hamilton, how the defendants wanted to proceed. Hamilton responded that the defendants did not resist the attorney general’s motion for default because he was not prepared to go to trial that day. The attorney general presented testimony of its witnesses to provide a basis for the court’s ultimate ruling.

II. Resolution of the Issues.

A. Denial of the continuance. On October 31, 2001, over a year and a half after the attorney general’s petition was filed, and only nineteen days before the trial date of November 19, the defendants moved for a continuance of the trial. The court denied the continuance, and the defendants raise this as an issue on appeal. The attorney general responds that (1) any argument regarding the continuance motion was waived by the defendants’ stipulation to a default; and (2) in any event, such rulings are discretionary with the trial court.

Under Iowa Rule of Civil Procedure 1.911(1), a continuance may be granted “for any cause not growing out of the fault or negligence of the movant, which satisfies the court that substantial justice will be more nearly obtained.” Rulings on continuance motions are left to the discretion of the district court and are presumed to be correct. A party challenging such a ruling carries a heavy burden. Rattenborg v. Montgomery Elev. Co., 438 N.W.2d 602, 605 (Iowa Ct.App.1989).

In this case, the court was justified in denying the continuance because the defendants had already slowed the progress of the case by disregarding the court’s scheduling order and by failing to comply with the court’s orders of March 8 and October 26, 2001, regarding discovery. The court also rejected the defendants’ argument that they needed a continuance to allow a new attorney to prepare for trial because the defendants had been dilatory in attempting to find new counsel. We agree with this conclusion as well.

We conclude the district court did not abuse its discretion in denying the motion for continuance.

B. The federal preemption claim. The defendants’ second issue raises a claim of federal preemption under the Medical Device Amendment (MDA) to the Federal Food, Drug, and Cosmetic Act. The defendants raised this issue in a mo *596 tion for summary judgment, which was denied. They now raise the court’s denial of their summary-judgment motion in this appeal. The federal statute on which the defendants rely provides:

State and local requirements respecting devices
(a) General rule
Except as provided in subsection (b) of this section [not applicable here], no State or political subdivision of a State may establish or continue in effect with respect to a device intended for human use any requirement—
(1) which is different from, or in addition to, any requirement applicable under this chapter to the device, and
(2) which relates to the safety or effectiveness of the device or to any other matter included in a requirement applicable to the device under this chapter.

21 U.S.C. § 360k.

In a case under the MDA, raising a similar preemption issue, the Supreme Court noted:

[B]ecause the States are independent sovereigns in our federal system, we have long presumed that Congress does not cavalierly pre-empt State-law causes of action. In all pre-emption cases, and particularly in those in which Congress has “legislated ... in a field which the States have traditionally occupied,” we “start with the assumption that the historic police powers of the States were not to be superseded by the Federal Act unless that was the clear and manifest purpose of Congress.”

Medtronic, Inc. v. Lohr, 518 U.S. 470, 485, 116 S.Ct. 2240, 2250, 135 L.Ed.2d 700, 715 (1996) (quoting Rice v. Santa Fe Elev. Corp., 331 U.S. 218, 230, 67 S.Ct.

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679 N.W.2d 593, 2004 Iowa Sup. LEXIS 156, 2004 WL 1058157, Counsel Stack Legal Research, https://law.counselstack.com/opinion/state-ex-rel-miller-v-new-womyn-inc-iowa-2004.