United States v. Gold

470 F. Supp. 1336, 13 ERC 1097, 9 Envtl. L. Rep. (Envtl. Law Inst.) 20713, 13 ERC (BNA) 1097, 1979 U.S. Dist. LEXIS 12906
CourtDistrict Court, N.D. Illinois
DecidedApril 20, 1979
Docket77 CR 1073
StatusPublished
Cited by73 cases

This text of 470 F. Supp. 1336 (United States v. Gold) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. Gold, 470 F. Supp. 1336, 13 ERC 1097, 9 Envtl. L. Rep. (Envtl. Law Inst.) 20713, 13 ERC (BNA) 1097, 1979 U.S. Dist. LEXIS 12906 (N.D. Ill. 1979).

Opinion

MEMORANDUM

LEIGHTON, District Judge.

In this criminal prosecution, an eleven-count indictment charges six individuals and a corporation, all in one count and all or some in other counts, with conspiracy to make, and with having made fraudulent statements, false representations to, and having concealed material matters from a governmental agency; and with violations of the Mail Fraud Act. Defendants have jointly filed 47 pretrial motions, 14 of them directed against the indictment because of alleged defects of form and substance.

In one motion to dismiss, supported by memoranda, exhibits and affidavits, defendants alleged that the grand jury which returned this indictment had an unauthorized person in the grand jury room. They allege that while Bingham Kennedy acted as a Special Attorney for the Department *1339 of Justice presenting the government’s case to the grand jury, he was at the same time on the staff of the Environmental Protection Agency, the complaining party in the criminal charges being investigated; that he was in the employ of the agency, and represented it in administrative proceedings in which the corporate defendant was a party; and that he became an important witness who alternated his position from that of a prosecutor to that of a person who testified and furnished evidence on which the grand jury returned the indictment in this case. These serious allegations, and the nature of the government’s response to them, led this court to conclude that an evidentiary hearing was required. Accordingly, a hearing has been had at which witnesses have testified and a large number of exhibits have been offered and received. 1 The issue that arises is whether the evidence adduced requires dismissal of this indictment.

I.

A.

Velsicol Chemical Corporation is engaged in the production, distribution, and sale of various pesticide chemicals, including heptachlor and chlordane, of which in this country it is the sole manufacturer. The national distribution, sale, and use of pesticide chemicals is regulated by the United States Environmental Protection Agency that functions pursuant to certain federal laws. The most important of these are the Federal Insecticide, Fungicide, and Rodenticide Act, amended in October 1972, 7 U.S.C. § 136, et seq., and §§ 408, 409 of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. §§ 346a, 348. 2 A pesticide chemical cannot be manufactured, distributed or sold within the United States without being registered with the Administrator of EPA upon compliance with the requirements of FIFRA. The same statute governs the cancellation and suspension of registered pesticide chemicals; and in section 6(a)(2), it is provided that “[i]f at any time after the registration of a pesticide the registrant has additional factual information regarding unreasonable adverse effects on the environment of the pesticide, he shall submit such information to the Administrator.” 7 U.S.C. § 136d(aX2). Sections 408 and 409 of the Federal Food, Drug and Cosmetic Act regulate the tolerance that is permitted in the use of a pesticide chemical, in or on a raw agricultural commodity. These provisions require that a petitioner for the tolerance established by the Administrator of EPA furnish data, including reports of investigations made with respect to the safety of a pesticide chemical. 21 U.S.C. § 346a(dXl)(C). A petition for a food additive tolerance must “contain full reports of investigations made with respect to the safety for use of such additive, including full information as to the methods and controls used in conducting such investigations.” 21 U.S.C. § 348(b)(2)(E).

In 1971, in fact for a long time before and throughout the period alleged in this indictment, heptachlor and chlordane were registered by the Administrator of EPA for distribution and sale in the United States. Defendants Harvey S. Gold, Charles J. Calo, John C. Tapas, Kenneth L. Schulz, and Neil R. Mitchell were Velsicol executives, all of them acquainted with and having varying degrees of responsibilities for the corporation’s compliance with the regulatory requirements of FIFRA as they pertain to the *1340 registration of heptachlor and chlordane. Defendant Bernard H. Lorant, during the same time, was a Velsicol attorney similarly involved.

Sometime in June 1971, at EPA’s suggestion and in order to answer questions concerning whether heptachlor was tumorigenic or carcinogenic in man or laboratory animals, Velsicol entered into an agreement with the International Research and Development Corporation of Mattawan, Michigan 3 for the administration of an 18 month feeding study in mice using a mixture of heptachlor and hetachlor epoxide, a metabolite of heptachlor. Later that year, in December 1971, Velsicol again contracted with IRDC for the administration of a similar 18 month feeding study in mice for chlordane. Slides from some two thousand animals were involved in the studies. IRDC made reports; and thereafter, between December 1972 and January 1973, Velsicol retained two consulting pathologists, Dr. John Rust of the University of Chicago and Dr. Paul Newberne of the Massachusetts Institute of Technology, to examine slides of liver tissues from mice used in the heptachlor and chlordane studies. In a report to Velsicol dated December 29, 1972, Dr. Rust, from a review of 50 IRDC slides, concluded “it is quite clear that the test animals were subjected to a severe hepatoxin and carcinogen.” In a report completed at approximately the same time, Dr. Newberne found among 22 IRDC slides he examined “liver cell carcinomas.” 4

On October .15, 1973, in the course of an administrative proceeding, Velsicol submitted to EPA a copy of IRDC’s final report concerning the feeding study of mice in which heptachlor had been used. This “show[ed] a compound-related incidence of nodular hyperplasia of the liver but no induction of cancer.” In the same month that this report was given to EPA, Velsicol employed Dr. William MacDonald of the University of Miami in Coral Gables, Florida, a consulting toxicologist, to examine for tumorigenicity all of the IRDC slides from the carcinogenicity study of heptachlor. In September 1974, Dr. MacDonald’s employment was extended to include an examination for tumorigenicity of all IRDC slides from the carcinogenicity study of chlordane. IRDC’s final report of its carcinogenicity study on chlordane was received by Velsicol during the month of December 1973. In the months of June and October 1974, Dr.

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Bluebook (online)
470 F. Supp. 1336, 13 ERC 1097, 9 Envtl. L. Rep. (Envtl. Law Inst.) 20713, 13 ERC (BNA) 1097, 1979 U.S. Dist. LEXIS 12906, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-v-gold-ilnd-1979.