Borskey v. Medtronics Inc ( 1996 )


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  •                     UNITED STATES COURT OF APPEALS
    FOR THE FIFTH CIRCUIT
    _____________________________________
    No. 95-30303
    _____________________________________
    ELAINE BORSKEY, ET AL.; JAMES A. BORSKEY; LEON PIERSON;
    TERESA PIERSON; PEGGY MORAN; JAMES MORAN, and all
    similarly situated,
    Plaintiffs-Appellants,
    VERSUS
    MEDTRONICS, INCORPORATED,
    Defendant-Appellee
    VERSUS
    SANOFI WINTHROP PHARMACEUTICALS,
    Defendant.
    ______________________________________________________
    Appeal from the United States District Court
    for the Eastern District of Louisiana
    (94-CV-2302)
    ______________________________________________________
    December 9, 1996
    Before DAVIS and DUHÉ, Circuit Judges and DOWD1, District Judge.
    PER CURIAM:2
    1
    District Judge of the Northern District of Ohio, sitting by
    designation.
    2
    Pursuant to Local Rule 47.5, the court has determined that
    this opinion should not be published and is not precedent except
    1
    Appellants challenge the district court's judgment rejecting
    their   claim   for    damages    for   personal       injuries   predicated   on
    Louisiana products liability law and RICO.                    The district court
    rejected the RICO action on grounds that RICO has no applicability
    to an action for damages from personal injuries.                We agree and for
    reasons stated by the district court in its March 13, 1995 order
    affirm the dismissal of the RICO claim.
    The district court dismissed appellants' products liability
    action as preempted under the Medical Device Amendments of 1976 to
    the Federal Food, Drug and Cosmetic Act. 21 U.S.C. § 301 et seq.
    Some time later, the Supreme Court issued a decision in Medtronics,
    Inc. v. Lohr, 513 U.S. ___, 
    116 S. Ct. 2240
    , 
    135 L. Ed. 2d 700
    (1996),   which    addresses      the   scope     of    the    MDA's   preemption
    provision, 21 U.S.C. § 360k(a).
    Section      360k(a)    of     the     MDA    prohibits       states   from
    "establish[ing] or continu[ing] in effect with respect to a device
    intended for human use any requirement" that is "different from, or
    in addition to, any requirement applicable under this chapter to
    the device" and that "relates to the safety or effectiveness of the
    device or to any other matter included in a requirement applicable
    to the device."       21 U.S.C. § 360k(a).        In Lohr, a plurality found
    that "[n]othing in § 360k denies [a state] the right to provide a
    traditional damages remedy for violations of common-law duties when
    under the limited circumstances set forth in Local Rule 47.5.4.
    2
    those duties parallel federal requirements."       
    Lohr, 116 S. Ct. at 2255
    .   The dissent agreed, stating that state law "claims are not
    pre-empted by § 360k to the extent that they seek damages for [a
    defendant's] alleged violation of federal requirements."          
    Id. at 2264.
    To the extent that the appellants' state law actions set forth
    violations   of   federal   requirements,   they   are   not   preempted.
    However, any other state law claims appellants wish to assert must
    be assessed individually in light of Lohr to determine § 360k's
    preemptive effect.     This sort of analysis should be initially
    undertaken by the district court, guided by the Lohr decision.
    Thus, we vacate and remand the judgment of the district court on
    appellants' products liability claims for further consideration in
    light of Lohr and this opinion.
    AFFIRMED IN PART, VACATED AND REMANDED IN PART.
    3
    

Document Info

Docket Number: 95-30303

Filed Date: 12/16/1996

Precedential Status: Non-Precedential

Modified Date: 4/18/2021