Jones v. C R Bard Incorporated

District Court, D. Arizona·Decided November 27, 2023·No. 2:23-cv-00535·Unknown

Opinion

WO

Ecila Jones, No. CV-23-00535-PHX-DWL

Plaintiff, ORDER

v.

C R Bard Incorporated, et al.,

Defendants. In this action, Plaintiff Ecila Jones (“Plaintiff”) asserts product liability claims against Defendants C. R. Bard, Inc. and Bard Peripheral Vascular, Inc. (collectively, “Defendants”) related to a medical device known as the Recovery Filter, which is an inferior vena cava (“IVC”) filter. Now pending before the Court is Defendants’ motion to dismiss Plaintiff’s complaint on statute-of-limitations grounds. (Doc. 11.) For the following reasons, the motion is granted and this action is terminated. I. Relevant Factual Allegations In The Complaint The facts set forth below, presumed true, are derived from Plaintiff’s operative pleading, the complaint. (Doc. 1.) Defendants are responsible for the design and manufacture of a medical device known as the Recovery Filter, which is an IVC filter. (Id. ¶¶ 3-4, 9-15.) The complaint contains extensive allegations concerning the defects in the Recovery Filter and Defendants’ knowledge of those defects. (See, e.g., id. ¶¶ 29-57.) In November 2004, a Recovery Filter was implanted in Plaintiff. (Id. ¶ 58.) On March 3, 2020, Plaintiff underwent a CT scan, which showed that her Recovery Filter “had tilted within” her IVC, that “[t]hree of the struts had fractured,” that “[o]ne of the broken struts was now embedded in the wall of the IVC,” and that “the other two had migrated and were in the right pulmonary arteries.” (Id. ¶ 59.) From at least this date onward, Plaintiff has experienced pain and suffering and other forms of damages. (Id. ¶ 61 [“The fragmented device has caused and will continue to cause Plaintiff pain and suffering, loss of ability to enjoy life, and economic loss.”].) On June 4, 2020, Plaintiff underwent surgery in an attempt to remove her fractured Recovery Filter. (Id. ¶ 60.) The procedure was not fully successful. (Id. [“Dr. Scott Trerotola attempted to retrieve the Bard Recovery Filter. The procedure took more than twice the normal amount of time expected for retrieval of an IVC filter. Dr. Trerotola was able to retrieve the filter and the three broken legs. However, one of the ‘feet’ from a strut was retained in the extravascular soft tissue and was unable to be removed.”].) Based on these allegations, the complaint asserts five claims: (1) manufacturing defect; (2) strict liability design defect; (3) negligent design; (4) strict liability information defect; and (5) negligent failure to warn. (Id. ¶¶ 66-113.) The complaint also includes a section entitled “Fraudulent Concealment.” (Id. ¶¶ 114-125.) The relevant factual allegations in that section are that (1) “Defendants marketed the Recovery Filter as being safer and less likely to fracture, migrate, or tilt than other devices, including the Simon Nitinol Filter [yet] concealed that they were aware of information suggesting the Recovery Filter was substantially more likely to fracture, migrate, tilt, or perforate the vena cava and other internal organs and cause injuries, than the other available IVC Filters”; (2) “Defendants were also aware at the time Plaintiff’s filter was distributed that electropolishing reduced the risk of fracture and that it was industry standard for Nitinol medical devices [yet] concealed that the Recovery Filter was not electropolished from Plaintiff and her physicians”; (3) “Defendants were also aware that numerous deaths and serious injuries had been confirmed to have been caused by failures of Bard Recovery filters [yet] concealed this information from Plaintiff and her physicians [and] only warned that people with filters had been reported to die and suffer serious injuries but not that any of these events were confirmed to have been caused by Bard’s filters”; (4) “Bard also concealed information that it knew internally there were design issues relating to stability and structural integrity with the Recovery Filter was creating quality problems and device failures once implanted and that Bard was about to introduce a new device that it claimed addressed these problems”; and (5) “Defendants also marketed the filter to the medical community and Plaintiff’s health care providers as if the device was safe and effective for the off-label uses for which it was used in this case [yet] concealed from consumers that these were off-label uses that had never been cleared by the FDA.” (Id. ¶¶ 116-20.) The complaint further alleges that “Plaintiff could not reasonably have discovered the claims made herein until, at the earliest, late 2022 when Plaintiff received notice of this information” and that “[a]ny applicable statutes of limitation have been tolled by the knowing and active concealment and denial of material facts known by Bard when they had a duty to disclose those facts.” (Id. ¶¶ 121, 124.) II. Procedural History On March 30, 2023—that is, more than two years after the unsuccessful removal surgery—Plaintiff initiated this action by filing the complaint. (Doc. 1.) On June 2, 2023, Defendants filed the pending motion to dismiss. (Doc. 11.) On June 30, 2023, Plaintiff filed a response. (Doc. 17.) Enclosed as an attachment to the response is a declaration from Plaintiff. (Doc. 17-1.) In relevant part, Plaintiff avows that she was advised by an unnamed doctor in 2018 that she “should get the filter removed” (id. ¶ 3); that she “saw a commercial on television about IVC filter litigation” in early 2019, called “the number provided,” and spoke to a representative of the Laborde Earles law firm (id. ¶¶ 4-5); that she received a series of letters in 2019 and 2020 from that law firm and a related law firm, Fears Nachawati, that led her to believe she “had retained legal representation, [her] interests were being protected, and [she] was pursuing a claim against the manufacturer of my IVC filter” (id. ¶¶ 5-9); that when she called Fears Nachawati in July 2022 “for an update on [her] case,” she was “told they were not [her] lawyers,” which caused Plaintiff to be “confused” (id. ¶ 12); and that “[t]he same day [she] was told this by Fears Nachawati, [she] started calling other lawyers who handled these types of cases” and eventually retained her current counsel (id.). On July 21, 2023, Defendants filed a reply. (Doc. 20.) Neither side requested oral argument. Under Rule 12(b)(6), “to survive a motion to dismiss, a party must allege sufficient factual matter, accepted as true, to state a claim to relief that is plausible on its face.” In re Fitness Holdings Int’l, Inc., 714 F.3d 1141, 1144 (9th Cir. 2013) (internal quotation marks omitted). “A claim has facial plausibility when the plaintiff pleads factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Id. (quoting Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009)). “[A]ll well-pleaded allegations of material fact in the complaint are accepted as true and are construed in the light most favorable to the non-moving party.” Id. at 1444-45 (citation omitted). However, the court need not accept legal conclusions couched as factual allegations. Iqbal, 556 U.S. at 678-80. Moreover, “[t]hreadbare recitals of the elements of a cause of action, supported by mere conclusory statements, do not suffice.” Id. at 678. The court also may dismiss due to “a lack of a cognizable legal theory.” Mollett v. Netflix, Inc., 795 F.3d 1062, 1065 (9th Cir. 2015) (citation omitted). Defendants argue (Doc. 11 at 5-6), and Plaintiff does not dispute (Doc. 17 at 7-9), that Plaintiff’s claims in this action are governed by Arizona’s two-year statute of limitations for personal-injury actions. See A.R.S. §§

Jones v. C R Bard Incorporated, (D. Ariz. 2023).

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