Anita Laux v. Mentor Worldwide, LLC
This text of Anita Laux v. Mentor Worldwide, LLC (Anita Laux v. Mentor Worldwide, LLC) is published on Counsel Stack Legal Research, covering Court of Appeals for the Ninth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Opinion
NOT FOR PUBLICATION FILED UNITED STATES COURT OF APPEALS NOV 26 2019 MOLLY C. DWYER, CLERK U.S. COURT OF APPEALS FOR THE NINTH CIRCUIT
ANITA LAUX, No. 17-56832
Plaintiff-Appellant, D.C. No. 2:16-cv-01026-ODW- AGR v.
MENTOR WORLDWIDE, LLC, MEMORANDUM*
Defendant-Appellee.
Appeal from the United States District Court for the Central District of California Otis D. Wright, II, District Judge, Presiding
Submitted November 18, 2019**
Before: CANBY, TASHIMA, and CHRISTEN, Circuit Judges.
Anita Laux appeals pro se from the district court’s summary judgment in her
diversity action alleging state law claims arising from alleged defects in her breast
implants manufactured by Mentor Worldwide, LLC. We have jurisdiction under
28 U.S.C. § 1291. We review de novo. Kohler v. Bed Bath & Beyond, LLC, 780
* This disposition is not appropriate for publication and is not precedent except as provided by Ninth Circuit Rule 36-3. ** The panel unanimously concludes this case is suitable for decision without oral argument. See Fed. R. App. P. 34(a)(2). F.3d 1260, 1263 (9th Cir. 2015). We may affirm on any basis supported by the
record. Id. We affirm.
Summary judgment was proper for Mentor on each of Laux’s state law
claims because Laux failed to raise a genuine dispute of material fact as to whether
Mentor violated a Food and Drug Administration (“FDA”) requirement, and
therefore her state law claims are expressly preempted under the Medical Device
Amendments (“MDA”) to the Food, Drug, and Cosmetic Act. See Weber v.
Allergan, Inc., 940 F.3d 1106, 1111 (9th Cir. 2019) (“[F]or a state law claim
regarding a Class III medical device[, such as breast implants,] to survive express
preemption by the MDA, a plaintiff must establish that the defendant violated an
FDA requirement.”).
The district court did not abuse its discretion by excluding the opinions of
Laux’s proffered expert witnesses because their opinions failed to satisfy the
requirements of Federal Rule of Evidence 702. Wendell v. GlaxoSmithKline LLC,
858 F.3d 1227, 1231-32 (9th Cir. 2017) (setting forth standard of review and
admissibility requirements for expert opinion testimony under Rule 702, as
explained in Daubert v. Merrell Dow Pharm., Inc., 509 U.S. 579 (1993)); see also
Yeti by Molly, Ltd. v. Deckers Outdoor Corp., 259 F.3d 1101, 1106 (9th Cir. 2001)
(district court may exclude information by an expert witness “required to be
disclosed by [Federal Rule of Civil Procedure] 26(a) that [was] not properly
2 17-56832 disclosed”).
The district court did not abuse its discretion by denying Laux’s motion for
leave to amend her complaint because amendment would have caused an undue
delay, prejudiced Mentor, and been futile. See Desertrain v. City of Los Angeles,
754 F.3d 1147, 1154 (9th Cir. 2014) (setting forth standard of review and factors
for determining whether to grant leave to amend).
We do not consider matters not specifically and distinctly raised and argued
in the opening brief, or arguments and allegations raised for the first time on
appeal. See Padgett v. Wright, 587 F.3d 983, 985 n.2 (9th Cir. 2009).
Laux’s motion to supplement the record on appeal is denied. See Gonzalez
v. United States, 814 F.3d 1022, 1031 (9th Cir. 2016) (“Absent extraordinary
circumstances, we generally do not permit parties to supplement the record on
appeal.”).
Mentor’s motion to strike references to portions of deposition transcripts that
are not part of the record on appeal is denied as unnecessary.
AFFIRMED.
3 17-56832
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