Gaillard v. Bayer Corp.

986 F. Supp. 2d 241, 2013 WL 6512044, 2013 U.S. Dist. LEXIS 176469
CourtDistrict Court, E.D. New York
DecidedDecember 13, 2013
DocketNo. 12-CV-3838 JFB GRB
StatusPublished
Cited by7 cases

This text of 986 F. Supp. 2d 241 (Gaillard v. Bayer Corp.) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Gaillard v. Bayer Corp., 986 F. Supp. 2d 241, 2013 WL 6512044, 2013 U.S. Dist. LEXIS 176469 (E.D.N.Y. 2013).

Opinion

MEMORANDUM AND ORDER

JOSEPH F. BIANCO, District Judge:

Plaintiff Fedhia Gaillard (“plaintiff’) bring this personal injury action against defendants Bayer Corporation and Bayer Healthcare Pharmaceuticals, Inc. (“defendants” or “Bayer”), alleging that her exposure to Bayer’s radiology contrast dye, Magnevist, caused her to develop a disease known as nephrogenic systemic fibrosis (“NSF”). Plaintiff has voluntarily dismissed several claims and, thus, the only remaining claims are for negligence, strict liability-design defect, and strict liability-failure to warn. Defendants move for judgment on the pleadings, arguing that the remaining personal injury causes of action are time-barred.

For the reasons set forth below, the Court agrees with defendants that the allegations in the Third Amended Complaint (“TAC”) make clear that the claims are time-barred. In particular, Section 214-c(2) of the New York Civil Procedure Law and Rules establishes an exception to the general three-year statute of limitations, [243]*243which allows the period to commence from the date of discovery of the injury in cases involving “personal injury ... caused by the latent effects of exposure to any substance.” C.P.L.R. § 214 — e(2).

The TAC alleges that plaintiff began developing significant symptoms from her exposure to Magnevist in June 2005, including “a localized thickening and tightness of the fingers and toes,” which spread over the next few months. (TAC ¶¶ 25-27.) Thus, because plaintiff discovered her injuries in June 2005, the filing of this lawsuit seven years later in August 2012 is well beyond the three-year statute of limitations period. Although plaintiff argues that the cause of her symptoms was not discovered until November 2009, it is well settled under New York law that the three-year period runs from the date that plaintiff first noticed symptoms of the injuries, not when the cause was diagnosed.

Moreover, plaintiff has not alleged facts that would satisfy the other relevant exception to the general three-year limitations period, which is set forth in Section 214-c(4). As a threshold matter, plaintiff failed to plead, as required under Section 214 — c(4), that medical knowledge sufficient to ascertain the cause of the injury had not been discovered before the expiration of the otherwise-applicable limitations period in June 2008. It is not surprising that no such allegation is made, given that a Multidistrict Litigation was formed in February 2008 (months before the limitations period ended in this case) consolidating dozens of cases alleging that Magnevist and other gadolinium-based contrast agents cause NSF.

Even if such an allegation were made, however, this exception could still not apply here because Section 214-c(4) also requires that the “discovery of the cause of the injury” be “alleged to have occurred less than five years after discovery of the injury.” C.P.L.R. § 214-c(4). In other words, plaintiff needed to allege that she identified Magnevist as the cause of her NSF symptoms in or before June 2010, which was five years from the date NSF symptoms led her to seek medical assistance. Plaintiff makes no such allegation.

Finally, even assuming arguendo that plaintiff was granted leave to re-plead and add such an allegation, she still could not fall within the exception because she did not file within one year from the discovery of the cause — at the latest, one year from June 2010 — and instead brought this lawsuit in August 2012. In an abundance of caution, at the oral argument, the Court gave plaintiff an opportunity to file a motion to re-plead to attempt to qualify for the Section 214-c(4) exception. However, plaintiff submitted a letter to the Court indicating that she did not wish the opportunity to file a motion to replead to attempt to address the statute of limitations issue. Accordingly, the motion to dismiss the remaining claims on statute of limitations grounds is granted.

I. Background

A. Factual Background

The following facts are taken from the TAC, and they are not findings of fact by the Court. The Court assumes these facts to be true for the purpose of deciding this motion, and construes them in the light most favorable to plaintiff, the non-moving party.

Plaintiff has a history of renal disease, for which she has undergone several Magnetic Resonance Imaging (MRI) procedures. (TAC ¶¶ 19-23.) During these procedures, plaintiff was exposed to defendants’ product Magnevist. (Id. at ¶ 5.) Magnevist is an injectable “gadolinium-based contrast agent” (id.) used during MRIs and angiography (id. at p. 1).

[244]*244Exposure to gadolinium is dangerous for renal-disease patients, like plaintiff, because they are less able to eliminate gadolinium from their bodies. (Id. ¶¶ 12-13.) As a result, products like Magnevist present a significant risk that renal disease patients might contract NSF. (Id. ¶ 12.) NSF1 is characterized by discoloration, thickening, tightening, and swelling of the skin within weeks or months of exposure to gadolinium. (Id. ¶ 37.) The skin changes begin as dark patches that eventually take on a “woody” texture, and are often accompanied by burning, itching, and severe pain. (Id.) NSF may also cause significant internal damage, and could result in death. (Id.) There is no known cure. (Id.)

Plaintiff was exposed to Magnevist on multiple occasions between 2001 and 2008. (Id. ¶¶ 20-23.) At some point, she began seeking treatment for an “increasingly worsening medical condition,” characterized by “hardening of her skin, joint stiffness, and corresponding limited range of motion.” (Id. at ¶ 24.)

In June of 2005, a physician diagnosed plaintiffs skin condition “as being consistent with sclerodactyly, a localized thickening and tightness of the skin of the fingers or toes.” (Id. ¶ 25.) The related condition of scleroderma was noted on plaintiffs hands that same month. (Id. ¶ 26.) Later in 2005, sclerodactyly was also found on plaintiffs legs. (Id. ¶¶ 27-28.) The condition persisted, but as late as October 2007, plaintiffs chronic pain, stiffness, and swelling were again diagnosed as scleroderma. (Id. ¶ 29.)

Many NSF patients are misdiagnosed multiple times before anyone discovers the disease. (Id. ¶ 16.) In plaintiffs case, NSF was raised as a possibility for the first time in September 2008, when her doctor recommended a biopsy. (Id. ¶ 30.) Plaintiff underwent that biopsy in August 2009, and in September 2009, her doctor suggested that she was suffering from NSF and encouraged her to seek a second opinion. (Id. ¶¶ 30-31.) Plaintiff did so, and the diagnosis was confirmed in November 2009, although plaintiff alleges that neither she nor her physicians understood the relationship between NSF and gadolinium at that time. (Id. ¶¶ 32-33.)

B. Procedural History

Plaintiff filed this lawsuit on August 2, 2012. She has amended the complaint three times. Defendant moved for judgment on the pleadings, and alternatively to dismiss the TAC, on July 15, 2013. Plaintiffs opposition was filed on September 6, 2013, and defendants’ reply was filed on September 16, 2013. The Court heard oral argument on this motion on November 26, 2013.

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Cite This Page — Counsel Stack

Bluebook (online)
986 F. Supp. 2d 241, 2013 WL 6512044, 2013 U.S. Dist. LEXIS 176469, Counsel Stack Legal Research, https://law.counselstack.com/opinion/gaillard-v-bayer-corp-nyed-2013.