Longs v. Wyeth

621 F. Supp. 2d 504, 2009 U.S. Dist. LEXIS 27112, 2009 WL 754524
CourtDistrict Court, N.D. Ohio
DecidedMarch 20, 2009
DocketCase No.: 1:03 CV 2042
StatusPublished
Cited by4 cases

This text of 621 F. Supp. 2d 504 (Longs v. Wyeth) is published on Counsel Stack Legal Research, covering District Court, N.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Longs v. Wyeth, 621 F. Supp. 2d 504, 2009 U.S. Dist. LEXIS 27112, 2009 WL 754524 (N.D. Ohio 2009).

Opinion

ORDER

SOLOMON OLIVER, JR., District Judge.

Plaintiff Ramona Longs (“Plaintiff’ or “Longs”) brings the above-captioned lawsuit as executor of the estate of decedent Mary Buchanan (“Buchanan”), alleging product liability claims regarding the diet pill Redux against Defendants Wyeth, et al. (collectively, “Defendants” or “Wyeth”). Now pending before the court are Plaintiffs Motion to Vacate Order and Judgment (ECF No. 151) and Plaintiffs Motion to Alter Judgment Pursuant to Federal Rule of Civil Procedure 59(e) (ECF No. 152). For the reasons discussed below, both Motions are denied.

I. FACTS AND PROCEDURAL HISTORY

A more detailed discussion of the facts appears in the court’s Order of February 28, 2008. (Order, ECF No. 29.) In that Order, the court granted summary judgment in favor of Defendants on all of Plaintiffs claims, finding that the strict liability and negligence claims related to pre-FDA approval were preempted by federal law and that the claims that were not preempted failed on their merits. Specifically, the court held that Plaintiffs strict liability design defect claim failed because Plaintiff had neglected to provide evidence to refute Defendants’ showing that the Redux warnings were adequate as a matter of law. The court also held that Plaintiffs negligence claims failed because Plaintiff had neglected to provide evidence of proximate cause. The court then denied Defendants’ Motions for Summary Judgment on Plaintiffs request for punitive damages as moot. By the same Order, the court also dismissed Plaintiffs failure to warn claim with prejudice on the ground that Plaintiff had voluntarily dismissed this claim. As a result of these rulings, the court dismissed Plaintiffs case in its entirety.

On March 10, 2008, Plaintiff filed the two pending Motions. In her Motion to *507 Vacate Order and Judgment (ECF No. 151), Plaintiff requests that the court vacate its Order dismissing Plaintiffs case as well as its Judgment Entry for Defendants so that the court could consider Plaintiffs Motion to Alter Judgment (ECF No. 152). In her Motion to Alter Judgment, Plaintiff raises the following arguments: (1) Plaintiffs claims are not preempted; (2) Defendants bear the burden of proof regarding whether the warnings were inadequate; (3) Defendants did not properly raise the argument that Plaintiff lacked evidence of the inadequacy of warnings with regard to her design defect claim; and (4) Defendants did not properly raise the issue that Plaintiff lacked evidence of proximate cause related to her negligence claims.

II. STANDARD FOR ALTERING OR AMENDING JUDGMENT

Rule 59(e) motions may be granted in the following instances: (1) clear error of law; (2) newly discovered evidence; (3) an intervening change in controlling law; or (4) to prevent manifest injustice. E.g., GenCorp, Inc. v. Am. Int’l Underwriters, 178 F.3d 804, 834 (6th Cir.1999). Although the court has authority to do so, a court will only reconsider its prior ruling in rare and unusual circumstances. As the court stated in Dana Carp. v. United States, 764 F.Supp. 482, 489 (N.D.Ohio 1991):

Although ‘motions to reconsider are not ill-founded step-children of the federal court’s procedural arsenal,’ they are ‘extraordinary in nature and, because they run contrary to notions of finality and repose, should be discouraged.’ In re August, 1993 Regular Grand Jury, 854 F.Supp. 1403, 1406 (S.D.Ind.1994). To be sure, ‘a court can always take a second look at a prior decision; but ‘it need not and should not do so in the vast majority of instances,’ especially where such motions ‘merely restyle or re-hash the initial issues.’ Id. at 1407. It is not the function of a motion to reconsider either to renew arguments already considered and rejected by a court or ‘to proffer a new legal theory or new evidence to support a prior argument when the legal theory or argument could, with due diligence, have been discovered and offered during the initial consideration of the issue.’ Id. at 1408. Where, as is the case with much of the instant motion, ‘defendant views the law in a light contrary to that of this Court,’ its ‘proper recourse’ is not by way of a motion for reconsideration ‘but appeal to the Sixth Circuit.’

McConocha v. Blue Cross and Blue Shield Mut. of Ohio, 930 F.Supp. 1182, 1184 (N.D.Ohio 1996). Motions to reconsider are “not designed to give an unhappy litigant an opportunity to relitigate matters already decided, nor is it a substitute for an appeal.” Sherwood v. Royal Ins. Co. of Am., 290 F.Supp.2d 856, 858 (N.D.Ohio 2003).

III. LAW AND ANALYSIS A. Preemption

1. Pre-FDA Approval Claims

The court previously granted in part and denied in part Defendants’ Motion for Partial Summary Judgment Based on Federal Preemption. (See Order, ECF No. 148, at 4-8.) Specifically, the court held that “all claims relating to pre-FDA approval are preempted by the FDA [or FDCA]. In addition, to the extent that Plaintiff alleges fraud-on-the-FDA or that Defendants concealed or misrepresented information to the FDA, these claims are preempted as well.” (Id. at 6.) The court’s conclusion was based on its finding that “Plaintiffs strict liability and negligence claims that Redux was an ‘unreasonably dangerous’ drug for which no warning would have *508 been adequate directly conflicts with the FDA’s authority to determine which drugs are sufficiently safe and effective to be marketed.” (Id.) However, the court also found that “Plaintiffs posi-FDA approval design defect claims, under strict liability and negligence, are not preempted.” (Id. at 7) (emphasis added.)

Plaintiff now argues that the court erred in finding that her claims relating to Defendants’ conduct prior to the FDA’s approval of Redux were preempted. In support of her argument for reconsideration, Plaintiff asserts that two recently decided Supreme Court cases bear on the preemption issues in the instant case. As discussed below, the court finds that these cases do not warrant a reconsideration of the court’s original ruling on preemption.

In Riegel v. Medtronic, Inc., — U.S. -, 128 S.Ct. 999, 169 L.Ed.2d 892 (2008), the plaintiff sued a medical device manufacturer for wrongful death, arguing that the device was defectively designed and labeled. The Court held that the Medical Device Act, 21 U.S.C. § 360k(a), expressly preempted common law claims regarding the safety and effectiveness of the device. The Court also noted that

State requirements are pre-empted under the MDA only to the extent that they are “different from, or in addition to” the requirements imposed by federal law. § 360k(a)(l). Thus, § 360k does not prevent a State from providing a damages remedy for claims premised on a violation of FDA regulations; the state duties in such a case “parallel,” rather than add to, federal requirements.

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Arrowood Indemnity Co. v. Lubrizol Corp.
695 F. App'x 842 (Sixth Circuit, 2017)
Wimbush Ex Rel. Estate of Buchanan v. Wyeth
619 F.3d 632 (Sixth Circuit, 2010)

Cite This Page — Counsel Stack

Bluebook (online)
621 F. Supp. 2d 504, 2009 U.S. Dist. LEXIS 27112, 2009 WL 754524, Counsel Stack Legal Research, https://law.counselstack.com/opinion/longs-v-wyeth-ohnd-2009.