Canning v. Medtronic Incorporated

District Court, D. Arizona·Decided April 12, 2022·No. 2:19-cv-04565·Unknown

Opinion

WO

Anthon y Canning, ) No. CV-19-04565-PHX-SPL ) ) Plaintiff, ) ORDER vs. ) ) ) Medtronic Incorporated, et al., ) ) Defendants. ) ) )

Before the Court is Plaintiff Anthony Canning’s (“Plaintiff”) Motion to Exclude (Doc. 137) and Motion for Leave (Doc. 124). In the Motion to Exclude, Plaintiff seeks to exclude the expert opinions of Michael Seger, M.D., and Jorge Ochoa, Ph.D. Plaintiff’s Motion for Leave, on the other hand, seeks leave to permit the late disclosure and testimony of Plaintiff’s purported rebuttal expert, Karl Leinsing. Plaintiff asserts that Mr. Leinsing’s testimony is only necessary in the event this Court denies Plaintiff’s Motion to Exclude and permits the testimony of Dr. Seger and Dr. Ochoa. Both of Plaintiff’s motions are fully briefed and ready for review. (Docs. 137, 143 & 144; Docs. 124, 131 & 133). After reviewing the parties’ briefing, the Court rules as follows. This is a products liability case arising from the use of a medical stapler gun during a surgical procedure performed on Plaintiff. (Doc. 13 at 2). The procedure—a robotic total gastrectomy during which Plaintiff’s stomach was surgically removed—took place on December 14, 2017 at Mayo Clinic Hospital (“Mayo”) in Phoenix, Arizona. (Id.). The stapler was an EEAXL2535 model stapler1 (a single-use device) that was designed and manufactured by Defendant. (Id.). After Plaintiff’s stomach was removed, the Mayo surgeons inserted the stapler into Plaintiff’s esophagus to create an “anastomosis”2 between his esophagus and his intestinal tract. (Id. at 3). The surgeons fired the stapler, but it failed to deploy staples. (Id.). As a result, Plaintiff’s esophagus was torn, and the anastomosis had to be completed by hand. (Id. at 4). Plaintiff suffered extended stays in the ICU, in the hospital, and in rehabilitation. (Id.). His pain was continuous and magnified by any attempts to swallow or breathe, and he will continue to suffer deterioration in his ability to intake adequate nutrition. (Id.). Following the surgery, the stapler was sent back to Defendant for inspection. (Id. at 3). Defendant inspected the stapler and found that it had been fired, and that it contained no staples. (Id.). Defendant installed staples, fired the stapler, and reported that it functioned properly. (Id.). Plaintiff now alleges that the stapler was delivered by Defendant to Mayo without staples, and that it was therefore defective. (Id.). On May 24, 2019, Plaintiff filed a Complaint against Defendant in the Superior Court of the State of Arizona. (Doc. 1-3 at 8). On June 26, 2019, Defendant removed the case to this Court. (Doc. 1 at 1). On July 23, 2019, Plaintiff filed an Amended Complaint containing two counts. (Doc. 13). Count I (“Negligence”) can be distilled to three claims: negligent design, negligent manufacture, and negligent failure to warn. (Id. at 5). Count II (“Strict Liability/Breach of Implied Warranty/Defect of Manufacture and Design”) can also be narrowed to three claims: strict-liability design defect, strict-liability manufacture defect, and breach of implied warranty. (Id.). ///

1 In their Joint Rule 26(f) Case Management Report, the parties more specifically identified the stapler as a DST Series™ EEA™ XL 25mm Single Use Stapler with 3.5 staples (reorder code EEAXL2535). (Doc. 20 at 2). 2 Plaintiff explains that an anastomosis “is a surgically created connection between two structures that are not normally connected.” (Doc. 137 at 3, n.3). Plaintiff’s theory of the case is that the stapler was delivered by Defendant to Mayo without staples and that it was therefore defective. Defendant contends that there were staples in the stapler or, at the least, that Plaintiff lacks evidence to prove the absence of staples. Plaintiff first seeks to exclude the opinions of two defense experts: Dr. Seger and Dr. Ochoa. If the Court denies that request and permits their testimony, Plaintiff alternatively requests that this Court grant him leave to permit the late disclosure and testimony of his purported rebuttal expert, Mr. Leinsing. The Court will address each motion in turn. A. Plaintiff’s Motion to Exclude Defendant’s Experts Plaintiff requests that this Court exclude the opinions of Dr. Seger and Dr. Ochoa under Federal Rule of Evidence (“FRE”) 402 because their testimony is irrelevant and because Defendant’s disclosure of them was in violation of certain state laws. Specifically, Plaintiff argues that how the stapler was used during Plaintiff’s procedure is not at issue in this case and that the stapler’s use is therefore irrelevant under FRE 401. (Docs. 137 at 2 & 144 at 3). Plaintiff also asserts that (i) Dr. Seger and Dr. Ochoa are not qualified under Arizona law to opine as to the care provided by the Mayo surgeons and (ii) their opinions place fault on Mayo and its surgeons, which violates the “nonparty-at-fault” deadline and prejudices Plaintiff. (Doc. 137 at 6). First, the Court rejects Plaintiff’s contention that the opinions of Dr. Seger and Dr. Ochoa are irrelevant. FRE 401 provides that evidence is relevant if “it has any tendency to make a fact more or less probable than it would be without the evidence” and “the fact is of consequence in determining the action.” Fed. R. Evid. 401. Likewise, FRE 702 requires that “expert testimony . . . be both relevant and reliable.” Messick v. Novartis Pharms. Corp., 747 F.3d 1193, 1196 (9th Cir. 2014) (citations omitted). “The relevancy bar is low, demanding only that the evidence ‘logically advances a material aspect of the proposing party’s case.’” Id. (quoting Daubert v. Merrell Dow Pharm., Inc., 43 F.3d 1311, 1315 (9th Cir. 1995)). “Relevancy depends on the particular law at issue because ‘[e]xpert opinion testimony is relevant if the knowledge underlying it has a valid connection to the pertinent inquiry.’” Id. (citing Primiano v. Cook, 598 F.3d 558, 565 (9th Cir. 2010)). Here, Plaintiff argues that Dr. Seger’s and Dr. Ochoa’s testimony is “only relevant and admissible if the Mayo surgeons’ acts, omissions, and/or fault is at issue for trial.” (Doc. 137 at 9). This argument implies that their testimony is concerned only with the conduct and liability of the surgeons, and not with anything else. At best, the Court finds Plaintiff’s argument to oversimplify their testimony; at worse, it misrepresents their testimony entirely. Dr. Seger’s and Dr. Ochoa’s testimony offers more than just opinions about the surgeons’ “acts, omissions, and/or fault.” For instance, Dr. Seger also opines about what to expect when a stapler is fired without staples. (Doc. 137-1 at 5). And Dr. Ochoa opines about the “six steps” in Defendant’s manufacture of the stapler where the presence of staples is checked. (Doc. 137-2 at 20). This testimony is clearly relevant to the issue of whether the stapler had staples in it—the pertinent inquiry in this product defect case. Even setting those examples aside, this Court finds no instance—in expert reports or in deposition testimony—where Defendant’s experts opine that the surgeons were at fault or otherwise measured their acts and omissions against any standard of care. Instead, their opinions focus on how the stapler was used and how it functioned during the procedure, and whether that usage provides any indication as to the presence of staples in t

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Canning v. Medtronic Incorporated, (D. Ariz. 2022).

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