United States v. Richlyn Laboratories, Inc.

365 F. Supp. 805, 18 Fed. R. Serv. 2d 630, 1973 U.S. Dist. LEXIS 11293
CourtDistrict Court, E.D. Pennsylvania
DecidedOctober 31, 1973
DocketCiv. A. 36583
StatusPublished
Cited by1 cases

This text of 365 F. Supp. 805 (United States v. Richlyn Laboratories, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. Richlyn Laboratories, Inc., 365 F. Supp. 805, 18 Fed. R. Serv. 2d 630, 1973 U.S. Dist. LEXIS 11293 (E.D. Pa. 1973).

Opinion

MEMORANDUM OPINION AND ORDER

EDWARD R. BECKER, District Judge.

This case has been closed for some two-and-a-half years. Presently before us is the government’s motion under rule 60(b), 1 F.R.Civ.P., to vacate this Court’s dismissal order of February 18, 1971, and to reopen the case and reinstate a preliminary injunction that was in force for over six years prior to the dismissal. The case arises under the Food, Drug, and Cosmetic Act 2 and was initiated by the government’s complaint for preliminary injunction filed September 30, 1964, which alleged certain inadequacies in the manufacture and processing of drugs at defendants’ plant. The preliminary injunction was entered by consent on October 9, 1967. 3 For several years the parties attempted to resolve their differences without a trial, but at no time did the government move to obtain a permanent injunction. On December 30, 1970, shortly after this case was reassigned to the undersigned, it was listed for a status call on January 7, 1971. Counsel were notified by mail and by publication in The Legal Intelligencer. Defense counsel responded with a letter dated December 31, 1970, stating:

To the best of my knowledge there is nothing further to be done in this matter. It has been entirely disposed of and I do not understand why it was listed.

The government did not appear for the status call, nor did it return the status call questionnaire. We viewed the government’s silence as acquiescence in the defense position, and believed the case to have been settled. In an effort to clear the case from the docket, we entered an order on February 18, 1971, dismissing the case with prejudice under local rule 23(b). 4 Copies of the order were sent by the clerk’s office to all parties.

*807 On November 2, 1972, the present motion was filed. In support of the motion, the government urges that it was unaware of the status call, of the defendant’s letter indicating the case was settled, and of the dismissal, until March 1972, when the Food and Drug Administration (FDA) “discovered” the dismissal and recommended to the United States Attorney in Philadelphia that he move to reinstate the injunction. Appended to the government’s brief are affidavits indicating that recent inspections of the defendant’s plant have, uncovered literally scores of deviations from the FDA’s “Current Good Manufacturing Practices,” which are published in the Code of Federal Regulations.

The government asks us to draw upon our reservoir of equitable power, codified in rule 60(b)(6), to grant relief, where justice so requires, from the operation of a judgment. For the reasons that follow, we decline the invitation to exercise that power and deny the government’s motion. Because the parties exhaustively briefed all issues raised by the motion, we will give only a succinct discussion of the several reasons for our decision, rather than review all the arguments expounded in the briefs.

The government’s delay in moving for finalization of the injunction resulted in the lawsuit’s becoming stale long, long ago. The drugs and specific violations forming the basis of the complaint are no longer involved in the affidavits submitted to us, which relate to more recent violations. The government’s current contempt petition is based on three shipments of Rauwolfia Serpentina in May and June of 1970 and one shipment of Estrand-Gens in January of 1971. These matters were not involved when the action was filed in 1964; indeed, neither of these drugs was involved in the original complaint, which referred to many other drugs. Thus, the facts alleged in the 1964 complaint and forming the basis for the consent injunction bear no relation to the facts existing eight years later when the motion to reinstate the injunction was filed. This state of affairs supports our conclusion that any further action by the government against the defendants can most appropriately be pursued in the context of a fresh lawsuit. In addition, we have serious reservations about the propriety and even the constitutionality of permitting the continuation for so long of a preliminary injunction so broad that it might give rise to strict liability, i. e., liability without scienter, in criminal contempt.

The government’s delay of twenty months in moving to reopen the case after entry of a 23(b) order also militates against reopening. Surely one touchstone of our judicial system is the principle of the finality of its judgments. Local Rule 23(b) allows ninety days for the filing of a motion to reopen a dismissed case. We find from the clerk’s notation on the dismissed order that a copy of the order was sent to the United States Attorney’s office. Furthermore, the government delayed its motion eight months after it became aware of the dismissal and long after March 1972, when we advised a representative of the FDA, who stopped by our chambers to inquire, that the proper way to reopen the ease was to file a motion.

The government’s failure to comply with our status call order would of itself justify dismissal, even if we had not believed the case settled. 5 We find that the United States Attorney’s office *808 did receive our three-page status call list. Furthermore, notice appeared in The Legal Intelligencer. 6 Thus, although the dismissal under rule 23(b) was technically inappropriate (see n. 4, supra), under the circumstances, equity requires that it be allowed to stand. Indeed, the Court’s power to dismiss a case in the circumstances presented here flows from several additional sources.

First, we have inherent power to dismiss a case on our own motion for want of prosecution. See Torino v. Texaco, Inc., 378 F.2d 268 (3d Cir. 1967). Second, rule 41(a) authorizes dismissal on the defendant’s motion for failure to prosecute or to comply with any order of court. Third, local rule 23(a) allows dismissal of an action in which no papers are docketed for two years — in this case, only the dismissal order interrupted a period of over two years without a docket entry. Want of prosecution is particularly burdensome to a defendant who remains under the force of a preliminary injunction.

Furthermore, the suitability of rule 60(b) relief in this case is questionable. A maximum of one year is allowed for a motion based on rule 60(b)(1): “mistake, inadvertence, surprise, or excusable neglect.” And 60(b)(6), “any other reason justifying relief,” under which the motion must be brought “within a reasonable time,” may not be used as a catchall to avoid the one-year limitation where 60(b)(1) applies. Gambocz v. Ellmyer, 438 F.2d 915 (3d Cir. 1971). Nor do we feel that the motion here was made within a reasonable time after discovery of the dismissal. As noted above, the government still delayed over seven months after we advised an FDA representative to file a motion. See

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Related

United States v. Richlyn Laboratories, Inc.
827 F. Supp. 1145 (E.D. Pennsylvania, 1992)

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Bluebook (online)
365 F. Supp. 805, 18 Fed. R. Serv. 2d 630, 1973 U.S. Dist. LEXIS 11293, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-v-richlyn-laboratories-inc-paed-1973.