Torbeck v. Zoon

CourtCourt of Appeals for the Fourth Circuit
DecidedAugust 29, 1997
Docket96-1962
StatusUnpublished

This text of Torbeck v. Zoon (Torbeck v. Zoon) is published on Counsel Stack Legal Research, covering Court of Appeals for the Fourth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Torbeck v. Zoon, (4th Cir. 1997).

Opinion

UNPUBLISHED

UNITED STATES COURT OF APPEALS

FOR THE FOURTH CIRCUIT

VICTOR H. TORBECK; WBI ENTERPRISES, INCORPORATED, formerly known as Worldwide Biologicals, Incorporated; NASHVILLE BIOLOGICALS, INCORPORATED, Plaintiffs-Appellants, No. 96-1962 v.

KATHRYN ZOON, Ph.D.; THOMAS S. BOZZO; GARY DYKSTRA; RONALD CHESEMORE; GERALD V. QUINNAN; DAVID KESSLER, Defendants-Appellees.

Appeal from the United States District Court for the District of Maryland, at Baltimore. Alexander Williams, Jr., District Judge. (CA-95-1761-AW)

Argued: May 7, 1997

Decided: August 29, 1997

Before WILKINSON, Chief Judge, MICHAEL, Circuit Judge, and COPENHAVER, United States District Judge for the Southern District of West Virginia, sitting by designation.

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Affirmed by unpublished per curiam opinion.

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COUNSEL

ARGUED: Philip Clyde Kimball, Louisville, Kentucky, for Appel- lants. Paige Elizabeth Harrison, Associate Chief Counsel for Enforce- ment, FOOD AND DRUG ADMINISTRATION, Rockville, Maryland, for Appellees. ON BRIEF: Lynne A. Battaglia, United States Attorney, Allen F. Loucks, Assistant United States Attorney, Baltimore, Maryland, for Appellees.

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Unpublished opinions are not binding precedent in this circuit. See Local Rule 36(c).

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OPINION

PER CURIAM:

Plaintiffs-Appellants Victor Torbeck, Nashville Biologicals, Inc. (NBI), and Worldwide Biologicals, Inc. (WBI) brought an action against six current and former employees of the United States Food and Drug Administration (FDA), seeking compensatory and punitive damages for an alleged deprivation of their rights under the Fifth Amendment's Due Process Clause. The district court determined that the plaintiffs' complaint did not allege a violation of clearly estab- lished rights and dismissed the action on the grounds of qualified immunity. We affirm.

I.

NBI and WBI are corporations which engaged in the business of collecting, storing, selling, and distributing human plasma and other blood products. Torbeck was the Chief Executive Officer of these companies as well as one of two shareholders. Defendants are all offi- cers of the FDA, the agency in charge of regulating and licensing plasma distributors. The complaint alleges that on May 5, 1992, one of the defendants notified WBI that the WBI plasmapheresis center in Fayetteville, North Carolina, had failed to pass an inspection and would not be allowed to continue operating. Torbeck sent a letter on May 21 requesting an abeyance of the suspension, but this request was denied in a letter from defendant Kathryn Zoon, a director at the FDA. According to the complaint, Zoon said that WBI would have its

2 license permanently revoked but would have an opportunity to contest this decision at a hearing. Plaintiffs claim to have requested both a hearing and information regarding the revocation. However, the FDA did not provide any of the information requested and did not schedule a hearing. On March 22, 1993, the FDA announced an opportunity for a hearing in the Federal Register but did not specify a date. See 58 Fed. Reg. 15351-53 (1993).

On April 29, 1994, Torbeck entered into a plea agreement for three counts of violating the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., and one count of making a false statement in violation of 18 U.S.C. § 1001. As part of the agreement, Torbeck agreed to the revocation of the WBI Fayetteville Center license.1

Concurrently with its investigation of WBI's Fayetteville Center, the FDA was also investigating NBI's plasmapheresis center located in Nashville, Tennessee. On September 30, 1992, the FDA suspended the Nashville Center's license to operate. Torbeck requested an abey- ance of the suspension, which was denied. On October 5, 1992, Tor- beck requested in a letter to the FDA that the license be revoked without a hearing.

Plaintiffs brought this action, pursuant to Bivens v. Six Unknown Named Agents of the Fed. Bureau of Narcotics, 403 U.S. 388 (1971), alleging that defendants had violated plaintiffs' constitutional rights under the Fifth Amendment's Due Process Clause by failing to pro- vide a hearing either before or promptly after the suspension of the licenses. Defendants moved to dismiss under Fed. R. Civ. P. 12(b)(6), asserting that they had qualified immunity from the suit. The district court agreed and dismissed the action. _________________________________________________________________

1 The complaint did not discuss the plea agreement; it said nothing about whether or how the WBI Fayetteville Center's license was ulti- mately revoked. At oral argument before the district court, however, plaintiffs acknowledged the plea agreement, and in their brief to this court they discuss the agreement in their Statement of Facts. See Brief for Appellants at 8.

3 II.

Plaintiffs claim that defendants violated their rights under the Due Process Clause by failing to provide the following: (a) a hearing prior to the suspension of the licenses, (b) a hearing promptly after the sus- pension of the WBI Fayetteville Center license, and (c) a hearing promptly after the suspension of the NBI Nashville Center license. We examine these claims in turn.

A.

In their complaint plaintiffs assert that defendants violated the Due Process Clause by "not provid[ing] Plaintiffs with any meaningful opportunity to be heard before shutting down the Fayetteville Center and the Nashville Center." J.A. 24. However, plaintiffs conceded before the district court that they had no right to a pre-suspension hearing. J.A. 47. Plaintiffs cannot revive that argument here. In any event, there are public health justifications for allowing FDA suspen- sions to take effect immediately. See, e.g., Ewing v. Mytinger & Cas- selberry, Inc., 339 U.S. 594, 598-600 (1950) (upholding seizures of misbranded articles under the Food, Drug & Cosmetics Act); North Am. Cold Storage Co. v. City of Chicago, 211 U.S. 306, 315-21 (1908) (upholding government authority to seize and destroy poten- tially infected food).

B.

Plaintiffs claim that defendants violated their right to due process by not providing a hearing within two years after the suspension of the WBI Fayetteville Center license. The license was suspended on May 5, 1992, and the FDA did not provide a hearing on that suspen- sion within the next two years. On April 29, 1994, Torbeck voluntar- ily agreed to rescind the license as part of a plea agreement.

Although we generally would have concerns about the constitution- ality of a two-year delay in granting a post-suspension hearing for a license to operate a business, we do not find that the district court erred in granting the defendants qualified immunity. Defendants are only liable for the violation of "clearly established statutory or consti-

4 tutional rights of which a reasonable person would have known." Harlow v.

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