Watson v. Mylan Pharmaceuticals, Inc.

701 F. App'x 729
CourtCourt of Appeals for the Tenth Circuit
DecidedJuly 13, 2017
Docket16-3349 & 17-3019
StatusUnpublished
Cited by1 cases

This text of 701 F. App'x 729 (Watson v. Mylan Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Tenth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Watson v. Mylan Pharmaceuticals, Inc., 701 F. App'x 729 (10th Cir. 2017).

Opinion

ORDER AND JUDGMENT *

Monroe G. McKay, Circuit Judge

In these consolidated appeals, Carmen Naomi Watson appeals pro se from district court orders that (1) denied her motion for a default judgment and instead dismissed her product-liability lawsuit against Mylan Pharmaceuticals, Inc. (Appeal No. 16» 3349); and (2) denied her post-judgment motion to recuse the district judge (Appeal No, 17-3019). Exercising jurisdiction under 28 U.S.C. § 1291, we affirm.

Background

Ms. Watson was allegedly injured by Mylan’s anti-acne drug, Amnesteem, an FDA-approved generic version of Accu-tane. In a pro se complaint, she sought $110,000,000 in damages, claiming she was not warned of Amnesteem’s dangerous side-effects, in violation of the Kansas Product Liability Act, Kan. Stat. Ann. §§ 60-3301 to -3307; the Kansas Consumer Protection Act, id. §§ 60-623 to -643; and Kansas common law.

Mylan moved to dismiss, arguing that Ms. Watson’s claims were preempted by federal law. See PLIVA, Inc. v. Mensing, 564 U.S. 604, 610-11, 624, 131 S.Ct. 2567, 180 L.Ed.2d 580 (2011) (finding preemption where state tort law required generic drug manufacturers to provide adequate warning labels but federal law required those manufacturers to use the same safety and efficacy labels as their brand-name counterparts); Mut. Pharm. Co. v. Bartlett, — U.S. —, 133 S.Ct. 2466, 2470, 186 L.Ed.2d 607 (2013) (“holding] that state-law design-defect claims that turn on the adequacy of a drug’s warnings are preempted by federal law under PLIVA”). In response, Ms. Watson suggested she was asserting design-defect claims, and she argued Mylan should have warned of Amnes-teem’s dangers by providing “extra precaution inserts.” R. at 58. Ms. Watson also sought a default judgment, arguing that Mylan had not timely answered her complaint or moved to dismiss.

While awaiting a ruling on its motion to dismiss, Mylan moved to stay discovery. Ms. Watson opposed a stay so she could seek evidence that Mylan had “failed to keep Amnesteem[’s] [warning label] updated.” R. at 101. A magistrate judge denied a stay to the extent Ms. Watson sought such evidence.

A month later, District Judge Carlos Murguia granted Mylan’s motion to dismiss, concluding that Ms. Watson’s claims *731 were preempted by federal law because “[i]t is impossible for generic drug manufacturers to comply both with state laws that would require alterations to a drug or its labeling to make the drug safer and with federal law that prohibits changes to approved drugs.” R. at 119. In dismissing Ms. Watson’s complaint, Judge Murguia did not address any failure-to-update issue. He also denied Ms. Watson’s motion for default judgment. Ms. Watson then unsuccessfully moved to recuse Judge Murguia as biased.

Ms. Watson now appeals, contesting the denials of her motions for default judgment and for recusal and the granting of Mylan’s motion to dismiss. 1

Discussion 2

I. Default Judgment

We review for an abuse of discretion the denial of a motion for default judgment. See Panis v. Mission Hills Bank, N.A., 60 F.3d 1486, 1494 (10th Cir. 1995). Ms. Watson contends she was entitled to a default judgment because Mylan’s motion to dismiss “had not been served by the due deadline.” Aplt. Opening Br. at 12 (Appeal No. 16-3349). But Mylan’s motion was mailed to Ms. Watson twenty-one days after she served her complaint. It was therefore timely. See Fed. R. Civ. P. 12 (providing that a motion to dismiss “must be made before pleading” and within twenty-one days after service of the summons and complaint); Fed. R. Civ. P. 5(b)(2)(C) (providing that “service is complete upon mailing”).

II. Dismissal

We review de novo a district court’s dismissal of a complaint for failure to state a claim, Jacobsen v. Deseret Book Co., 287 F.3d 936, 941 (10th Cir. 2002), examining whether the plaintiff has pled sufficient factual allegations “to state a claim to relief that is plausible on its face,” Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570, 127 S.Ct. 1955, 167 L.Ed.2d 929 (2007).

Ms. Watson first contends she was not “giv[en] the opportunity to present evidence” before the district court dismissed her complaint. Aplt. Opening Br. at 13 (Appeal No. 16-3349). But “[t]he 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 plaintiffs .., complaint alone is legally sufficient to state a claim for which relief may be granted.” Peterson v. Grisham, 594 F.3d 723, 727 (10th Cir. 2010) (internal quotation marks omitted).

Next, Ms. Watson argues her claims were not preempted. She attempts to avoid Mensling and Bartlett on the ground that the “warnings on the Amnes-teem box [she] received were outdated as the original drug maker had a history of revisions.” Aplt. Opening Br, at 15 (Appeal No. 16-3349). Granted, the Sixth Circuit has held that a failure-to-warn claim is not preempted if the generic drug’s warning label does not include language from the brand-name drug’s updated warning label. See Fulgenzi v. PLIVA, Inc., 711 F.3d 578, 584 (6th Cir. 2013). But see Morris v. PLIVA, Inc., 713 F.3d 774, 777 (5th Cir. 2013) (per curiam) (“[I]t is logically incoherent to contend that PLIVA had a duty *732 to apply the 2004 warning label when Appellants also assert repeatedly that no labels predating 2009 were adequate. Tort liability does not arise for failure to attach an inadequate label”). Ms. Watson did not, however, include failure-to-update allegations in her complaint. And she opposed dismissal of her complaint not on the basis of Mylan’s failure to update Amnesteem’s warning to correspond to Accutane’s warning, but on the basis that Mylan had failed to provide “extra precaution inserts” supplementing Accutane’s warnings. R. at 58. Even in a post-judgment motion for reconsideration, Ms. Watson claimed she had not received a warning insert and should have been given the “opportunity to submit this theory of inadequate warning.” Aplee. Supp. App.

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