Elmitha Pierre v. Intuitive Surgical, Inc.
Opinion
[DO NOT PUBLISH]
IN THE UNITED STATES COURT OF APPEALS
FOR THE ELEVENTH CIRCUIT
No. 20-11311
Non-Argument Calendar
D.C. Docket No. 0:18-cv-60095-RAR
ELMITHA PIERRE, MAXO JEAN JACQUES,
Plaintiffs-Appellants,
versus
INTUITIVE SURGICAL, INC., Defendant-Appellee,
Appeal from the United States District Court for the Southern District of Florida
(April 2, 2021)
Before ROSENBAUM, JILL PRYOR, and LUCK, Circuit Judges. PER CURIAM:
In this products-liability case, Elmitha Pierre and Maxo Jean Jacques allege that Pierre was injured by the Endowrist HotShears Monopolar Curved Scissors
(“Scissors”), an electrosurgical medical device manufactured and sold by Intuitive Surgical, Inc. They contend that Intuitive was both negligent and strictly liable for the Scissors’ defective design, and both negligent and strictly liable for failing to warn them of the resultant danger from the Scissors. The district court granted summary judgment to Intuitive, concluding that Pierre failed to present sufficient evidence that her injury was caused by the Scissors to prove her design-defect claims, and that, for her failure-to-warn claims, she did not show that the warnings were inadequate or that the alleged failure to warn was the proximate cause of her injuries. On appeal, Pierre argues that she presented sufficient evidence of causation to get to a jury on her design-defect claims. After careful review, we affirm the judgment in favor of Intuitive.
I.
Pierre suffered a thermal injury (a burn) to her bowel during a robotically assisted hysterectomy performed on January 24, 2014. Pierre’s surgeon, Dr. Yat- Min Chen, performed the surgery using the da Vinci Surgical System, a robotic surgical device manufactured and sold by Intuitive that allows a surgeon to conduct minimally invasive surgery using a variety of instruments, including electrosurgical instruments.
Intuitive manufactures electrosurgical laparoscopic instruments for use with the da Vinci system, including the Scissors, which use monopolar electric energy to
cut and coagulate tissue, and the Fenestrated Bipolar Forceps (“Forceps”), which use bipolar electric energy. 1 Both instruments were used in Pierre’s surgery. So too was a metal suction tube not manufactured by Intuitive and not docked to the da Vinci system.
Near the end of the surgery, Dr. Chen noticed that Pierre had suffered damage to her bowel. After realizing the damage to Pierre’s bowel, Dr. Chen requested a consultation from the general surgeon on call. The surgeon looked at Pierre’s tissue for approximately five minutes, determined there was not much damage, and recommended keeping her in the hospital for observation. As a result, no repairs were made to her bowel during the surgery. Six days later, however, Pierre began experiencing devasting physical side effects due to the damage to her bowel.
Pierre claims that the injury to her bowel was caused by electrical arcing from the Scissors due to an insulation defect in its shaft. She reached that conclusion in part because, less than a year before the surgery, Intuitive had voluntarily recalled older versions of the Scissors (versions 9 and 10) due to a potential for these instruments “to develop very small cracks (‘micro-cracks’) near the distal (scissor) end.” According to the recall notice, these micro-cracks, which “may not be visible
1 Monopolar energy is a type of energy characterized by the passage of a current from a single electrode at the tip of an electrosurgical instrument to tissue and through the patient to a return pad to complete the electric current circuit. Bipolar energy is a type of energy characterized by the confinement of electrical current to the tissue between the two electrodes of the instrument.
to the user,” “may create a pathway for electrosurgical energy to leak to tissue and potentially cause thermal injury.” While a newer version of the Scissors (version 12) was used in Pierre’s surgery, and it has not been subject to a recall, Pierre maintains that the same type of insulation defect in the older versions was also present in the version used in her surgery.
Several months after the surgery, in October 2014, Dr. Chen attended an advanced training course offered by Intuitive and, seeking to understand how Pierre’s injury had occurred, asked Dr. Pitter, the now-deceased instructor, to review Pierre’s videotaped hysterectomy procedure. After reviewing the video, according to Dr. Chen, Dr. Pitter concluded that the damage to Pierre’s bowel was most likely due to “arcing.” But Dr. Pitter did not state whether the arcing was from the Scissors or the Forceps, nor did he tell Dr. Chen that the Scissors used in Pierre’s surgery were defective.
Dr. Chen did not witness any arcing from any of the devices used during the surgery. He also testified that arcing, alone, does not necessarily indicate an insulation failure because arcing may come from either the tip of the instrument or the shaft of the instrument. And because arcing occurs quickly, it is difficult to determine from which end arcing comes.
Dr. Chen testified that he believed Pierre’s injury was caused by the metal suction tube conducting energy from one of the electrosurgical instruments to the
bowel. And in his view, the source of the energy was “the bipolar, because [he] didn’t fire the monopolar” at the time he believes the injury occurred. In other words, Dr. Chen believed that it was “more likely” that energy from the Forceps— not the Scissors—transferred to the metal suction tube, which was near Pierre’s bowel, and inadvertently conducted energy to the bowel.
II.
Pierre sued Intuitive in federal district court under diversity jurisdiction, see 28 U.S.C. § 1332, alleging Florida state-law claims of design defect and failure to warn under strict products-liability and negligence theories. 2 Intuitive filed a motion for summary judgment, which the district court granted in full. Only the design defect claims are at issue in this appeal.
In granting summary judgment on the design-defect claims, the district court explained that two elements of Pierre’s claims were disputed: (1) whether the Scissors were defective or unreasonably dangerous, or both; and (2) if so, whether such defect proximately caused Pierre’s injuries. As to the first issue, the court found that Pierre presented sufficient evidence to create a genuine issue of material fact as to whether the Scissors used in her surgery were defectively designed under Florida law. This evidence included “numerous adverse event reports” and returned
2 Jacques, Pierre’s husband, joined as a plaintiff alleging a derivative claim of loss of consortium.
instruments with microcracks associated with version 12 of the Scissors—the same version used in her surgery—and expert testimony that version 12 was not reasonably safe without incorporating Active Electrode Monitoring (“AEM”) technology or other coaxial shielding and monitoring of the shaft of the device.
But the district court found that Pierre’s claims failed for lack of proof of causation. The court stated that expert testimony was required to establish causation in this products-liability case, and that Dr. Chen was Pierre’s only expert on that issue. 3 But Dr. Chen’s testimony, in the court’s view, was insufficient for several reasons.
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