Atlantic Mutual Insurance v. American Academy of Orthopaedic Surgeons

734 N.E.2d 50, 315 Ill. App. 3d 552, 248 Ill. Dec. 342, 2000 Ill. App. LEXIS 591
CourtAppellate Court of Illinois
DecidedJuly 14, 2000
Docket1-98-2670
StatusPublished
Cited by70 cases

This text of 734 N.E.2d 50 (Atlantic Mutual Insurance v. American Academy of Orthopaedic Surgeons) is published on Counsel Stack Legal Research, covering Appellate Court of Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Atlantic Mutual Insurance v. American Academy of Orthopaedic Surgeons, 734 N.E.2d 50, 315 Ill. App. 3d 552, 248 Ill. Dec. 342, 2000 Ill. App. LEXIS 591 (Ill. Ct. App. 2000).

Opinion

JUSTICE QUINN

delivered the opinion of the court:

Plaintiffs, Atlantic Mutual Insurance Company (Atlantic Mutual) and Centennial Insurance Company (Centennial), filed a complaint for declaratory judgment seeking a determination of whether they owed defendants, the American Academy of Orthopaedic Surgeons (AAOS) and the Scoliosis Research Society (SRS) (collectively, defendants), a duty to defend or indemnify them for civil conspiracy and concert of action claims brought against them in underlying mass product liability litigation. Defendants filed a motion to dismiss plaintiffs’ complaint for failure to name necessary parties which the trial court denied. The trial court also denied defendants’ motion to compel discovery of various documents and witnesses. Subsequently, plaintiffs filed a motion for summary judgment and argued that they had no duty to defend or indemnify defendants in the underlying suit. The triad court granted summary judgment in favor of plaintiffs and ruled that the causes of action contained in the underlying suit were not covered under the insurance policies issued to AAOS and SRS; therefore, plaintiffs had no duty to defend or indemnify AAOS and SRS. On appeal, defendants contend that: (1) Atlantic Mutual and Centennial have a duty to defend AAOS and SRS where the underlying complaint does not allege that AAOS and SRS “expected or intended” to injure the underlying plaintiffs; (2) the trial court erred in denying defendants’ motion to dismiss for failure to join necessary parties; and (3) the trial court abused its discretion in ruling on plaintiffs’ motion for summary judgment without allowing defendants to complete written discovery and depose witnesses. For the reasons that follow, we affirm.

The underlying litigation involves numerous cases brought against AAOS, SRS and others as a result of complications from the implantation of pedicle screw fixation devices. The complaints have been consolidated into a multidistrict litigation action entitled, In re: Orthopaedic Bone Screw Products Liability Litigation, which is currently pending in the United States District Court for the Eastern District of Pennsylvania. 1

Pedicle screw fixation devices are designed to be used in spinal fusion surgery. These devices are used to fuse two or more vertebrae together in order to correct various spinal conditions. According to the underlying complaint, pedicle screw fixation devices are classified by the Food and Drug Administration (FDA) as Class III devices, which means that they “present a potential unreasonable risk of illness or injury” and therefore must receive premarket approval from the FDA before they may be commercially sold or distributed. In order to generate the required scientific evidence to allow approval, the FDA granted pedicle screw manufacturers permission to conduct numerous clinical trials from 1986 through 1993. According to the underlying complaint, these clinical trials failed to provide sufficient evidence to support a successful application for premarket approval. The underlying complaint alleges that, despite the lack of premarket approval for these devices, pedicle screw manufacturers promoted, marketed, distributed, and sold devices that were intended for use as pedicle screw fixation devices. The complaint further alleges that hundreds of thousands of individuals were surgically implanted with these devices despite a lack of adequate evidence that these devices were safe and effective when used in this manner. r

AAOS is a professional organization comprised of orthopaedic surgeons, some of whom spécialize in spine surgery. SRS is a professional organization comprised of spine surgeons who are admitted to membership by invitation only. AAOS and SRS are named defendants in approximately 500 of these pedicle screw fixation device cases. Civil conspiracy and concert of action claims were specifically brought against AAOS and SRS.

The civil conspiracy claim alleges that from the middle of 1988 through early 1989 pedicle screw manufacturers and various medical societies, including AAOS and SRS, “reached an agreement, understanding, and a meeting of the minds” to pursue an “intercompany/ association conspiracy” which was described as follows:

“The purpose of the intercompany/association conspiracy, to which each member of the conspiracy agreed, was to promote, market, distribute, and sell medical devices intended for use as pedicle screw fixation devices, to do so through deceptive and misleading means and thereby to:
a) cause pedicle screw fixation devices to be introduced, delivered and/or received in interstate commerce as Class III devices without premarket approval ***;
b) promote such devices as pedicle screw fixation devices and represent to spine surgeons that such devices were safe and effective when used as pedicle screw fixation devices, even though such devices were ‘investigational devices’ *** and pedicle screw fixation surgery was an ‘investigational use’ under FDA regulations; and
c) engage in deception.”

The underlying complaint further alleges that AAOS and SRS, along with other professional associations, participated in the conspiracy because “they recognized that they could capitalize on the manufacturers’ interest in promoting pedicle screw fixation devices through the associations by obtaining significant financial compensation and remuneration from manufacturers for doing so.” The underlying complaint then alleges the following:

“The participating manufacturers and sellers of pedicle screw fixation devices would provide the participating professional associations and others with grants, contributions, fees, and other remuneration to sponsor or conduct seminars, workshops, conferences and symposia which were directed to spine surgeons and which promoted pedicle screw fixation surgery.
5-4 5}4 :$4
*** [U]nder the scheme adopted and implemented pursuant to the intercompany/association conspiracy, these seminars, workshops, conferences and symposia were really sales events where those who participated in the intercompany/association conspiracy attempted to create or expand a market for the sale of pedicle screw fixation devices and to obtain from the participants sales of the devices for use in pedicle screw fixation surgery.”

The complaint alleges that, by engaging in such deceptive conduct, defendants acted in reckless disregard of the risk that the acts in furtherance of the conspiracy would result in the distribution of medical devices that were untested and unproven for their intended use and exposed numerous plaintiffs in the underlying complaints to substantial and serious risks of painful and disabling injuries.

Regarding causation and injury, the complaint alleges that the purpose of the intercompany/association conspiracy was “to cause *** pedicle screw fixation devices to be placed into commerce and to be used in patients” and that “as a direct, proximate and reasonably foreseeable result, *** plaintiff has suffered and will continue to suffer physical harm.”

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Bluebook (online)
734 N.E.2d 50, 315 Ill. App. 3d 552, 248 Ill. Dec. 342, 2000 Ill. App. LEXIS 591, Counsel Stack Legal Research, https://law.counselstack.com/opinion/atlantic-mutual-insurance-v-american-academy-of-orthopaedic-surgeons-illappct-2000.