O'CONNELL v. Biomet, Inc.

250 P.3d 1278, 2010 Colo. App. LEXIS 359, 2010 WL 963234
CourtColorado Court of Appeals
DecidedMarch 18, 2010
Docket09CA0224
StatusPublished
Cited by30 cases

This text of 250 P.3d 1278 (O'CONNELL v. Biomet, Inc.) is published on Counsel Stack Legal Research, covering Colorado Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
O'CONNELL v. Biomet, Inc., 250 P.3d 1278, 2010 Colo. App. LEXIS 359, 2010 WL 963234 (Colo. Ct. App. 2010).

Opinion

Opinion by

Judge CASEBOLT.

In this action against a medical device manufacturer and its sales representative, plaintiffs, Kerry O'Connell (O'Connell) and Anne O'Connell, appeal the summary judgment in favor of defendants, Biomet, Inc., EBI, LP., and John Kyger, on their claims of negligence and strict lability failure to warn. We conclude that the trial court correctly applied the "learned intermediary" doctrine in the context of the failure to warn claim and correctly held that product warnings need be given only to O'Connell's physician. We further conclude that the trial court correctly applied the "captain of the ship" doctrine. We decline to address plaintiffs' claim that there is a genuine issue of material fact that precludes summary judgment on the adequacy of the warning, because they did not present to the trial court the argument they now assert on appeal. Accordingly, we affirm.

I. General Background

O'Connell fractured his elbow. His physician, Dr. Christopher Brian, recommended surgery to repair the fracture. To provide range of motion for the affected joint during the healing process, Dr. Brian decided to use an external elbow fixator called the EBI OptiROM, manufactured by EBI, a wholly owned subsidiary of Biomet.

*1280 The fixator, a medical device regulated by the federal Food and Drug Administration, may only be sold by or upon the order or prescription of a physician. EBI provided a package insert and a surgical technique manual with the fixator describing installation techniques, risks, and potential adverse events in the use and application of the device. During the surgery, EBI's sales representative, John Kyger, who physically delivered the fixator, was present in the operating room.

Dr. Brian applied the fixator to O'Connell's humerus using bone screws, during which the drill bit or the bone serew pierced his radial nerve, wound it up, and tore a section of it out of his arm, resulting in permanent injury. After the surgery, Dr. Brian wrote a letter to Biomet and EBI regarding O'Con-nell's surgical injury and recommended revisions to the surgical technique manual in an effort to prevent future occurrences of that type of injury.

Plaintiffs asserted and settled a claim against Dr. Brian. Plaintiffs released Dr. Brian, his surgical assistant, his practice group, and all of Dr. Brian's "agents." Plaintiffs later filed this action, asserting negligence, strict liability failure to warn, design defects, breach of implied warranty, and loss of consortium.

Defendants moved to dismiss the negli-genee claim against Kyger, asserting that he was one of Dr. Brian's "agents" under the "captain of the ship" doctrine and was therefore covered under the terms of the release. They also moved for partial summary judgment on the failure to warn claim, asserting that the warnings and instructions in the package insert and surgical technique manual were adequate as a matter of law. Treating the motion to dismiss as a motion for summary judgment, the trial court granted the motions. It subsequently granted summary judgment on the remaining claims. This appeal followed.

IL Standard of Review

Summary judgment is appropriate only when the pleadings and supporting documents clearly demonstrate that there are no genuine issues of material fact, and that the moving party is entitled to judgment as a matter of law. C.R.C.P. 56(c); Cotter Corp. v. American Empire Surplus Lines Ins. Co., 90 P.3d 814, 819 (Colo.2004). Factual disputes will not defeat summary judgment if the disputed facts are not material to the outcome of the case. Svanmidge v. Kirken-dall, 169 P.3d 262, 264 (Colo.

In the determination of a summary judgment motion, "[the nonmoving party is entitled to the benefit of all favorable inferences that may be drawn from the undisputed facts, and all doubts as to the existence of a triable issue of fact must be resolved against the moving party." Martini v. Smith, 42 P.3d 629, 682 (Colo.2002).

We review a grant of summary judgment de novo. West Elk Ranch, L.L.C,. v. United States, 65 P.8d 479, 481 (Colo.2002).

IIL Failure to Warn Claim

Plaintiffs first contend that the trial court erred in applying the "learned intermediary" doctrine in holding that defendants had a duty to warn only Dr. Brian. They also contend that, even if the court correctly applied that doctrine, there are nevertheless genuine issues of material fact as to whether defendants provided adequate warnings and instructions to surgeons about the dangers and installation of the elbow fixator. We conclude that the trial court correctly applied the learned intermediary doctrine. We decline to address the contention that genuine issues of material fact are present here because we conclude that plaintiffs failed to assert before the trial court the argument they make in their opening brief, and the argument they made in the trial court is not asserted on appeal.

A. General Law

A failure to warn adequately can render a product, which is otherwise free of defect, defective for purposes of strict liability recovery. Barton v. Adams Rental, Inc., 988 P.2d 532, 539 (Colo.1997); Hiigel v. General Motors Corp., 190 Colo. 57, 63, 544 P.2d 983, 987 (1975); see Restatement (Second) of Torts § 402A emt. j (1965) ("In order to prevent the product from being unreasonably *1281 dangerous, the seller may be required to give directions or warning, on the container, as to its use.").

The plaintiff has the burden of proving that the manufacturer gave an inadequate warning of the danger that caused the injury. Peterson v. Parke Davis & Co., 705 P.2d 1001, 1004 (Colo.App.1985).

B. Nature of the Duty

Ordinarily, a manufacturer has a duty to warn all foreseeable ultimate users of dangers inherent in its products. See Hiigel, 190 Colo. at 63, 544 P.2d at 987; Restatement (Second) of Torts § 888. However, where prescription drugs are concerned, the manufacturer's duty to warn has been limited to an obligation to advise the prescribing physician of any potential dangers that may result from the drug's use. Reyes v. Wyeth Laboratories, 498 F.2d 1264, 1276 (5th Cir.1974). The physician is trained to assess the risks and benefits of the drug as applied clinically to a particular patient. See id. This principle is the learned intermediary doctrine. See Sterling Drug, Inc. v. Cornish, 370 F.2d 82, 85 (8th Cir.1966).

No Colorado appellate opinion has addressed the learned intermediary doctrine directly. However, in Peterson, 705 P.2d at 1003, the division, in analyzing the propriety of a product misuse defense, noted that the warnings contained in a prescription drug manufacturer's package insert were addressed to the physician. See also Hamilton v.

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Bluebook (online)
250 P.3d 1278, 2010 Colo. App. LEXIS 359, 2010 WL 963234, Counsel Stack Legal Research, https://law.counselstack.com/opinion/oconnell-v-biomet-inc-coloctapp-2010.