TED STEWART, District Judge.
The matter before the Court is Defendant St. Jude Medical, Inc.'s ("St. Jude") Motion to Dismiss for Failure to State a
Plaintiff Richard McCartney ("McCartney") is a veteran who suffered back injuries during his military service in the mid-1980s. As a result of these injuries, McCartney has suffered nerve damage and chronic leg pain. In 2010, McCartney was informed of a possible treatment to assist him with chronic leg pain. On January 3, 2011, McCartney underwent a trial surgery to implant a temporary spinal cord stimulator (the "stimulator") at the VA Medical Center in Salt Lake City (the "VA") in order to determine if he would be a good candidate for a permanent implant. McCartney received approximately 50% relief from his leg pain and was deemed a good candidate for the permanent implant. St. Jude is the manufacturer of the stimulator and provided the stimulator to the VA to implant in McCartney's back. Erik Hall and Mikelle Mabey ("Mabey") are St. Jude representatives who allegedly "assist surgeons to implant the medical products, and assist patients who receive the medical products."
On May 17, 2011, McCartney underwent a surgery to implant a permanent stimulator in his back. Dr. Paul Amstutz ("Dr. Amstutz"), a neurosurgeon at the VA performed the surgery. Initially, the stimulator worked well to control Plaintiff's pain, which was located in the top rear of his left leg down to his left foot, but the effectiveness decreased progressively. By mid-August 2011, the stimulator did not work at all. On December 16, 2011, an X-ray indicated that at least one of the stimulator wires was fractured.
On April 17, 2012, McCartney underwent another surgery at the VA to correct the problem with the permanent stimulator. A St. Jude representative was present during the surgery and allegedly called McCartney's wife during the surgery to inquire about the location of McCartney's pain. McCartney's wife indicated that she was unsure which leg was afflicted. After the surgery, the stimulator was turned on but did not address McCartney's pain. McCartney could feel the device working on the upper front side of his right leg. Allegedly, St. Jude representatives told McCartney that the stimulator was placed in an incorrect location. McCartney saw a different VA physician, Dr. Isani, in November 2012. Dr. Isani allegedly told McCartney that the stimulator paddle was placed on the wrong side of Plaintiff's spinal cord.
In February 2013, McCartney underwent another surgery to replace the spinal stimulator yet again. Dr. Levitt, a private doctor not associated with the VA, conducted the surgery to replace the stimulator. The surgery was successful.
This suit arises out of the two surgeries performed by Dr. Amstutz. Plaintiff brings two causes of action for negligence against both St. Jude and the United States of America. St. Jude seeks dismissal.
In considering a motion to dismiss for failure to state a claim upon which relief can be granted under Rule 12(b)(6), all well-pleaded factual allegations, as distinguished from conclusory allegations, are accepted as true and viewed in the light
"The court's function on a Rule 12(b)(6) motion is not to weigh potential evidence that the parties might present at trial, but to assess whether the plaintiff's complaint alone is legally sufficient to state a claim for which relief may be granted."
Plaintiff asserts two negligence claims against Defendants collectively, one for each allegedly negligently performed surgery. A claim for negligence requires four elements: a duty, breach of that duty, causation, and damages.
There is a relatively new, yet now common practice, of having medical device company representatives attend surgeries.
"Duty must be determined as a matter of law and on a categorical basis for a given class of tort claims."
In determining whether a duty exists between medical device manufacturers and patients, B.R. ex rel. Jeffs v. West is particularly instructive. In Jeffs the Utah Supreme Court determined that physicians owe nonpatients a duty to exercise reasonable care in prescribing medications that pose a risk of injury to third parties.
In support of the first cause of action, which corresponds to the May 2011 surgery, Plaintiff alleges, "On information and belief, the Company's employees instructed Dr. Amstutz as to how to implant the permanent spinal cord stimulator in Plaintiff's back."
Plaintiff is left only with the allegation that Defendants failed to ensure that the physician properly implanted the stimulator device and electrodes. This cause of action is one for St. Jude's nonfeasance during McCarney's surgery. Upon a review of the duty factors in the case at hand, the Court concludes that there is no special legal relationship between medical device manufacturers and patients such that medical device manufacturers owe a duty of care for their nonfeasance during a physician's surgery. St. Jude did not owe Plaintiff a duty to ensure the physician properly implanted the medical device at issue. The Court will therefore grant St. Jude's Motion to Dismiss regarding Plaintiff's first count of negligence.
In support of the second count of negligence, which corresponds to the April 2012 surgery, Plaintiff alleges that during Plaintiff's surgery, St. Jude, "voluntarily undertook the duty to ensure that the electrodes would be placed in the proper location in Plaintiffs' [sic] back."
While St. Jude as a medical device manufacturer would ordinarily have no duty to ensure the physician placed the electrodes in the proper location, Plaintiff has alleged that by Mabey's communication with McCartney's wife during the surgery, St. Jude voluntarily undertook the duty to act reasonably. Plaintiff argues that this phone call establishes that St. Jude involved itself in medical decision-making in some affirmative way and therefore voluntarily undertook a duty. This cause of action is for St. Jude's alleged misfeasance during McCartney's surgery.
Liability for such an undertaking is outlined in the Restatement (Second) of Torts § 324A. Section 324A states,
The parties disagree about whether Section 324A is applicable. Even if the Court assumes that Section 324A applies, Plaintiff's claim still fails because there are no facts alleged that St. Jude acted unreasonably in its undertaking nor are there any facts alleged that anyone relied on St. Jude's undertaking.
Plaintiff's Complaint does not identify the wrongful acts allegedly committed by each Defendant. The use of the collective term "Defendants" fails to inform individuals what wrongful acts they allegedly committed.
Section 324A requires St. Jude to have acted unreasonably. Plaintiff does not allege any action by St. Jude other than Mabey having gathered information during a telephone call with McCartney's wife. As outlined above, Section 324A requires that harm be suffered "because of reliance of the other or the third person upon the undertaking." In the case at hand, that means that the harm caused by improperly implanting electrodes during the surgery must be suffered because Dr. Amstutz relied on the information Mabey provided. Plaintiff does not allege that Mabey gave Dr. Amstutz misinformation regarding Plaintiff's pain, nor does Plaintiff allege that Dr. Amstutz relied on said misinformation. Therefore, Plaintiff's allegations fail to demonstrate a claim under § 324A.
The Court is mindful that the exact conduct of St. Jude's representatives and Dr. Amstutz during the second surgery is not yet fully known. Discovery is necessary to determine each actor's conduct during the surgery. To that end, the Court will dismiss Plaintiff's second cause of action without prejudice so that if discovery reveals facts sufficient to show that Plaintiff suffered harm because the physician relied on St. Jude's failure to exercise reasonable care, Plaintiff may amend his Complaint to reassert claims against St. Jude.
Based on the foregoing, it is hereby
ORDERED that Defendant St. Jude's Motion to Dismiss (Docket No. 8) is granted.