Anderson v. Siemens Corporation

335 F.3d 466, 2003 WL 21434780
CourtCourt of Appeals for the Fifth Circuit
DecidedJuly 9, 2003
Docket02-10005
StatusPublished
Cited by27 cases

This text of 335 F.3d 466 (Anderson v. Siemens Corporation) is published on Counsel Stack Legal Research, covering Court of Appeals for the Fifth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Anderson v. Siemens Corporation, 335 F.3d 466, 2003 WL 21434780 (5th Cir. 2003).

Opinion

EMILIO M. GARZA, Circuit Judge:

Siemens Medical Systems, Inc. (“Siemens”), a corporation that sells and distributes medical devices, appeals from a jury’s verdict finding it liable, under a strict products liability (design defect) theory, to Sandra Jo Anderson (“Petitioner”) and the estate of her late husband, Billy D. Anderson (“Decedent”), for damages resulting from the stroke, in 1996, ¿nd subsequent death, in 1998, allegedly caused by the Siemens Servo 900C ventilator (“the ventilator”) used on Decedent following his 1996 cardiac bypass surgery. 1

Siemens argues that there was insufficient evidence to support the jury’s verdict, that the district court made erroneous evidentiary rulings, that the damages awarded by the jury were excessive, and that the district court abused its discretion by awarding Petitioner pre-judgment interest during “periods of delay” caused by Petitioner.

Carried with this case is Siemens’ motion to certify to the Texas Supreme Court the question of whether Texas would apply § 6(e) of the Restatement (Third) of Torts: Products Liability, under which “a retail seller or other distributor of a prescription drug or medical device” can be held strictly liable for a manufacturing defect and for negligent distribution, but not for a design defect. 2 Siemens argues that, if we do not certify the question, we should hold that Petitioner’s design defect claim is barred by § 6(e).

I

In May of 1996, Decedent underwent cardiac bypass surgery at St. Luke’s Hospital in San Antonio, Texas (“the Hospital”). According to Decedent’s surgeon, Dr. Lawrence Hamner (“Dr.Hamner”), the operation lasted slightly longer than a normal bypass operation, but was otherwise uneventful. Following the operation, Decedent’s blood pressure and heart rate readings were both normal. Decedent was placed in the intensive care unit (the “ICU”), where he was connected to the ventilator to support his breathing.

The ventilator had been sold by Siemens to the Hospital, who had made it available for use on patients. The ventilator can be set at different ventilation modes. The desired mode setting is selected using the ventilator’s mode selection knob. The ventilator is also equipped with several alarms, which are intended to alert medical personnel when a patient’s exhaled air drops below, or increases above, certain levels. Generally, a switch to the “manual” mode will trigger an alarm. Such an alarm is necessary because, in the manual mode, the ventilator does not support a *469 patient’s breathing and is the equivalent of turning the ventilator completely off.

The respiratory therapist, Misti Condit (“Condit”), set the ventilator in accordance with the settings prescribed by the anesthesiologist, Dr. Chistopher Duncan (“Dr. Duncan”). The settings prescribed by Dr. Duncan did not involve use of the manual mode. Around the time when Condit was attaching the ventilator to Decedent, the scene in the ICU became “harem scarem,” according to Dr. Hamner. The ICU nurses were attempting to attach other devices, including an EKG monitor and a blood pressure monitor, and the medical team was working frantically to fix the dopamine line and pulse oximeter, both of which were not functioning properly.

Within the first half hour that Decedent was in the ICU, a member of the medical team became aware that Decedent was no longer breathing. Dr. Duncan immediately disconnected Decedent from the ventilator and began manually ventilating him with an Ambu bag. When the matter was brought to Condit’s attention, she walked over from the nurses’ station, discovered that the ventilator was set in the manual mode, and immediately switched the mode back to its proper setting (the SIMV setting). 3 There had been no audible alarm alerting the medical team to the ventilator’s switch to the manual mode. 4

In the meantime, Decedent had gone into cardiac arrest. As a result, Decedent was forced to undergo two additional surgeries during the night. 5 When Decedent awoke from anesthesia the following morning, the Hospital staff determined that Decedent had suffered a severe stroke sometime after he was anesthetized for his first surgery, but before he awoke. Decedent remained hospitalized for several months. Thereafter, Decedent returned home to the care of his wife, Petitioner.

Approximately two years later, in April of 1998, Decedent died. Decedent’s death certificate, certified by Kerr County, lists “pneumonia” as the “IMMEDIATE CAUSE (Final disease or condition resulting in death).” As the “UNDERLYING CAUSE (disease or injury that initiated events resulting in death),” the death certificate lists “CVA” (i.e., cerebrovascular accident, or stroke) occurring “2 yrs” before death. The physician who prepared the death certificate certified in that document that, “To the best of my knowledge death occurred ... due to the cause(s) and manner stated.” 6

On behalf of herself and Decedent’s estate, Petitioner sued Siemens in Texas state court. 7 Siemens removed to federal *470 court, which exercised diversity jurisdiction pursuant to 28 U.S.C. § 1332. The ease then proceeded to a jury trial. The design defect question was submitted to the jury, who returned a verdict finding that (1) Petitioner proved that there was a design defect in the ventilator at the time it left the possession of Siemens that was a producing cause of Decedent’s 1996 stroke; (2) Petitioner proved that Decedent’s 1996 stroke was a producing cause of his death; (3) Siemens failed to prove that the negligence of the Hospital (through its respiratory therapist and/or its nurses) proximately caused Decedent’s 1996 stroke, or that the negligence of Dr. Duncan proximately caused Decedent’s 1996 stroke; (4) Siemens (the ventilator) caused 100% of the occurrence or injury (the Hospital caused 0%, and Dr. Duncan caused 0%); (5) Petitioner is entitled to $6 million in damages as compensation for her damages resulting from the injuries to Decedent; and (6) Decedent’s estate is entitled to $1 million in damages as compensation for injuries that resulted from “the occurrence in question.” The district court entered judgment, and subsequently denied Siemens’ motion for judgment as a matter of law, as well as its alternative motions for a new trial and for remittitur. Siemens timely appealed.

II

Siemens asks us to certify to the Texas Supreme Court the question of whether Texas would apply § 6(e) of the Restatement (Third) of Torts: Products Liability, under which “a retail seller or other distributor of a prescription drug or medical device” can be held strictly hable for a manufacturing defect and for negligent distribution, but not for a design defect. 8

It is within our discretion to certify a state law question to the relevant state supreme court. See Lehman Bros. v. Schein,

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Bluebook (online)
335 F.3d 466, 2003 WL 21434780, Counsel Stack Legal Research, https://law.counselstack.com/opinion/anderson-v-siemens-corporation-ca5-2003.