In Re Cutter Laboratories, Inc., Etc.

465 F. Supp. 1295, 1979 U.S. Dist. LEXIS 14102
CourtUnited States Judicial Panel on Multidistrict Litigation
DecidedFebruary 28, 1979
Docket367
StatusPublished

This text of 465 F. Supp. 1295 (In Re Cutter Laboratories, Inc., Etc.) is published on Counsel Stack Legal Research, covering United States Judicial Panel on Multidistrict Litigation primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Cutter Laboratories, Inc., Etc., 465 F. Supp. 1295, 1979 U.S. Dist. LEXIS 14102 (jpml 1979).

Opinion

OPINION AND ORDER

PER CURIAM.

This litigation presently consists of fifteen actions pending in eleven districts as follows:

*1296 Northern District of California 3 actions 1

Eastern District of New York 2 actions

Southern District of New York 2 actions

Northern District of Alabama 1 action

Northern District of Illinois 1 action

District of Kansas 1 action

Eastern District of Michigan 1 action

Western District of Michigan 1 action

Southern District of Mississippi 1 action

Northern District of New York 1 action

Eastern District of North Carolina 1 action

Cutter Laboratories, Inc. (Cutter) is the sole named defendant in fourteen of the above actions and is co-defendant with its insurance company in the remaining action. The plaintiffs in each action have all been users or spouses of users of a certain model of prosthetic heart valve marketed, until 1974, by Cutter under the trade name “Braunwald-Cutter.” The valve involved in each of these actions was used in the aortic position when implanted into a heart.

Generally, the plaintiffs in these actions allege that the valve users suffered severe injuries and/or death resulting from defects in the valve that caused the valve to wear out prematurely and to fail when used in the aortic position. Specific injuries alleged include major embolic complications arising from the premature wearing of the heart valve, premature open heart surgery to replace the heart valve or certain of its component parts, and catastrophic poppet (ball) escape from the heart valve cage. Liability against Cutter in each of the fifteen actions is based, inter alia, on theories of negligence in the design, manufacture, testing and sale of the valve; breach of express and implied warranties; and/or strict liability in tort.

Plaintiffs in the Illinois action move the Panel, pursuant to 28 U.S.C. § 1407, to transfer the thirteen actions pending in districts other than the Eastern District of New York to that district for coordinated or consolidated pretrial proceedings with the two actions pending there. 2 Plaintiffs in ten additional actions either join in or support the motion to centralize all actions in the Eastern District of New York. Cutter and plaintiffs in the three California actions oppose transfer. Alternatively, if the Panel finds transfer under Section 1407 to be appropriate in this litigation, Cutter favors selection of either the District of Minnesota or the Northern District of Alabama as the transferee forum. Plaintiffs in the California actions, in the event transfer is ordered by the Panel, favor the Northern District of California.

We find that these actions involve common questions of fact and that their centralization under Section 1407 in the Eastern District of New York will best serve the convenience of the parties and witnesses and promote the just and efficient conduct of the litigation.

Cutter argues that common questions of fact will not predominate in this litigation. Cutter urges that discovery on the issue of damages will be unique to each action and that, with respect to the issue of causation, Cutter will seek to establish that valve failure was patient related. Thus Cutter maintains that discovery in each action will focus on the following individual factors: the patient’s health and past medical history, the anti-coagulant therapy administered after the valve implant, and local medical practices. Cutter also urges that transfer in this litigation is unnecessary because most of the actions are proceeding expeditiously towards trial, with discovery completed or nearly completed, and trial dates soon to be set, in several actions. Finally, Cutter and plaintiffs in the California actions argue that voluntary cooperation among the parties, their counsel and the *1297 involved courts is a preferable alternative to transfer under Section 1407.

We are persuaded that centralized pretrial proceedings under Section 1407 are appropriate in this litigation. Although we recognize that some individual factual questions will be present in each action, an analysis of the record before us reveals a commonality of factual questions concerning the design, development, manufacture, testing and marketing of the BraunwaldCutter valve; the state of medical knowledge regarding heart valves; the causal relationship between the use of the Braunwald-Cutter valve in the aortic position and the severe injuries alleged to have resulted therefrom; Cutter’s knowledge of the allegedly defective condition of the valve; and the reasons behind Cutter’s decision in 1974 to remove the valve from the market. Thus centralization under Section 1407 is necessary in order to prevent duplication of discovery and eliminate the possibility of conflicting pretrial rulings. Any discovery unique to a particular party, action or claim can be scheduled by the transferee judge to proceed concurrently with the common discovery, thus enhancing the efficient conduct of the litigation. See In re A.H. Robins Co., Inc. “Daikon Shield” IUD Products Liability Litigation, 406 F.Supp. 540, 542 (Jud.Pan.Mult.Lit.1975). While voluntary cooperation among parties and their counsel is always commendable, transfer under Section 1407 will result in the assignment of all actions to a single judge who will be in the best position to determine the manner and extent of coordination or consolidation of the pretrial proceedings for the optimum conduct of the litigation as a whole. See In re Commonwealth Oil/Tesoro Petroleum Securities Litigation, 458 F.Supp. 225, 229 (Jud.Pan.Mult.Lit.1978).

Some parties have suggested that certain actions are sufficiently advanced to warrant their exclusion from transfer. All actions, of course, are not at the same stage of discovery, but based on the information before us, we conclude that all actions in this litigation will benefit from centralized pretrial proceedings under Section 1407. We observe that if and when an action or claim is, in fact, ready for trial or otherwise ready for remand because the transferee judge finds that the Section 1407 proceedings pertaining to that action or claim are completed, the transferee judge may suggest to the Panel that the Panel remand the action or claim to its transferor court. 28 U.S.C. § 1407(a); Rule ll(c)(ii), R.P.J.P. M.L., 78 F.R.D. 561, 569 (1978). See, e. g., In re A.H. Robins Co., Inc. “Daikon Shield” IUD Products Liability Litigation, 453 F.Supp. 108 (Jud.Pan.Mult.Lit.1978). Also, any discovery heretofore completed in any action may be made applicable to all actions by utilizing the procedures recommended in the Manual for Complex Litigation, Parts I and II, §§ 3.11 (rev.ed. 1977).

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Bluebook (online)
465 F. Supp. 1295, 1979 U.S. Dist. LEXIS 14102, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-cutter-laboratories-inc-etc-jpml-1979.