JOHN F. KEENAN, District Judge.
Before the Court is Plaintiff's motion for leave to file an amended complaint that adds Novartis Pharmaceuticals as a defendant. Novartis opposes the motion on the grounds that the amendment would be futile because the proposed claims against Novartis are time-barred. For the reasons that follow, Plaintiff's motion to amend the complaint is denied.
This MDL involves claims that the drug Fosamax or its generic equivalent, alendronate sodium, caused users to suffer from a condition known as osteonecrosis of the jaw ("ONJ"). Plaintiffs have asserted claims against Merck, the maker of Fosamax. Some plaintiffs have also brought claims against other bisphosphonate manufacturers.
The instant Plaintiff, Leanne Finlay, brings claims on behalf of her deceased mother, Carolee Corley ("Decedent"). Their action against Merck was originally filed in Florida state court on July 15, 2011. That case was transferred to the U.S. District Court for the District of New Jersey, and was later refiled here in the Southern District of New York. By stipulation between Plaintiff and Merck, the filing here relates back to July 15, 2011, when Plaintiff filed her initial case in Florida.
The extant complaint in this action, dated September 3, 2013, lists Merck and five unnamed "New Jersey Corporations" as defendants. Paragraph 11 states:
The extant complaint alleges in addition to Fosamax, Decedent had also taken Zometa, an intravenous bisphosphonate manufactured by Novartis. (Compl. ¶ 26.) But the complaint does not mention Novartis, and alleges only that Fosamax caused Decedent's injuries.
It is undisputed that Plaintiff and Novartis entered into a tolling agreement on September 19, 2013, sixteen days after the filing of the extant complaint. The agreement tolled the statute of limitations for claims by Plaintiff against Novartis that were timely as of that date, but Novartis expressly reserved the right to argue that Plaintiff's claims were already time-barred by then.
On May 30, 2014, the day before the tolling agreement expired, Plaintiff moved for leave to file an amended complaint inserting Novartis in place of one of the John Doe defendants. Novartis opposes the motion on the grounds that the amendment would be futile.
Rule 15(a)(2) of the Federal Rules of Civil Procedure governs the amendment of pleadings once the time for amendment as of right has elapsed. The Rule provides that leave to amend should be freely given "when justice so requires." Fed. R. Civ. P. 15(a)(2);
To decide whether Plaintiff's proposed amendments are futile, the Court must first determine the date on which Plaintiff should be deemed to have asserted claims against Novartis. If Plaintiff's claims relate back to the filing of the initial state court complaint, then they will be deemed timely if they were not time-barred as of July 15, 2011. If her claims against Novartis do not relate back, then they will be deemed timely only if they were not time-barred as of September 19, 2013, the date of the tolling agreement between Plaintiff and Novartis.
In moving to amend her complaint, Plaintiff seeks to substitute Novartis for one of the unnamed "John Doe" defendants. Under Rule 15(c), an amendment to a complaint that changes the name of a party in the complaint will relate back to the date of the original complaint if three conditions are met: (1) the amendment must assert a claim that arose out of the same conduct set out in the original complaint; (2) the new defendant must receive actual notice of the action within 120 days of when the original complaint was filed; and (3) the new defendant knew or should have known within 120 days of the original complaint being filed "that the action would have been brought against it, but for a mistake concerning the proper party's identity." Fed. R. Civ. P. 15(c)(1)(B)-(C).
Plaintiff asserts that Novartis has known about her claims "since the outset of this lawsuit." (Pl. Moving Br. ¶ 8.) This assertion apparently refers to the outset of the instant, federally filed suit. But there is nothing to indicate that Novartis was on notice of Plaintiff's claims within 120 days after the filing of the initial Florida complaint in 2011. Novartis represents that Plaintiff did not contact Novartis regarding her claims until September 2013. Plaintiff has not disputed this representation, and her moving brief is consistent with it. The brief notes that Plaintiff and Novartis exchanged information and documents in connection with their tolling agreement, which was executed on September 19, 2013. Under these circumstances, Plaintiff has failed to show that the requirements of Rule 15(c) are satisfied.
Nor does New York state's "unknown parties" law apply here. The provisions of New York's C.P.L.R. governing "John Doe" defendants allows:
N.Y. C.P.L.R. § 1024. To take advantage of this provision, the party must (1) "exercise due diligence, prior to the running of the statute of limitations, to identify the defendant by name," and (2) "describe the John Doe party in such form as will fairly apprise the party that [it] is the intended defendant."
In sum, the Court concludes that Plaintiff's proposed amendment does not relate back to the filing of the initial Florida complaint on June 15, 2011. Accordingly, her claims will be time-barred if they were untimely as of September 19, 2013, the date of the tolling agreement between Plaintiff and Novartis.
Having determined the operative date after which Plaintiff's putative claims against Novartis are time-barred, the Court must now ascertain the applicable statute of limitations for each of those claims. "When a federal district court sits in diversity, it generally applies the law of the state in which its sits, including that state's choice of law rules."
(1) negligence; (2) strict liability: failure to warn; (3) strict liability: defective design; (4) breach of express warranty; (5) breach of implied warranty; (6) fraud; (7) survival action; (8) loss of consortium; and (9) punitive damages. These claims are discussed in turn.
The New York statute of limitations for an action to recover damages for personal injury is three years. N.Y. C.P.L.R. § 214(5). The three-year period begins either when plaintiff discovered the injury or should have discovered it, whichever is earlier. § 214-c(2). Under Florida law, negligence claims are subject to a four-year statute of limitations. Fla. Stat. § 95.11(3)(a). This Court therefore applies the shorter three-year period under New York law.
Decedent's medical records reflect that she received four Zometa infusions between June 10, 2008 and September 2, 2008. (Novartis Br. at 4 & nn.5-7.) After Decedent began to complain of ONJ-like symptoms, both her oncologist and her oral surgeon noted the possible connection between her symptoms and the Zometa infusions. (
In New York, a plaintiff's product liability causes of action (both defective design and failure to warn) are subject to a three-year statute of limitations, which accrues on the date the injuries are discovered.
Under both New York and Florida law, breach of contract claims are subject to a four-year statute of limitations, running from when the breach occurs, is discovered, or should have been discovered.
The New York statute of limitations for actions based upon fraud is the greater of six years from the date the cause of the action accrued, or two years from the time the plaintiff discovered, or reasonably could have discovered, the fraud. N.Y. C.P.L.R. § 213(8). Florida has a four-year statute of limitations on fraud-based claims, running from when the fraud was (or should have been) discovered. Fla. Stat. § 95.11(3)(j); § 95.031(2)(a). This Court therefore applies Florida's four-year period.
As Novartis notes, the company revised its prescribing information to include a warning about ONJ in September 2003. To the extent any fraud persisted, however, it should have been discovered contemporaneously with Decedent's BRONJ diagnosis on October 17, 2008. Thus, any fraud claims against Novartis were barred as of October 17, 2012.
Generally speaking, a plaintiff cannot recover on a survival theory unless the underlying cause of action would be timely if asserted by the decedent.
In New York, a claim for loss of consortium is derivative, and is dependent upon a viable underlying or "primary" cause of action.
The Court also notes that Plaintiff does not appear to have a valid claim for loss of consortium under Florida law. Florida does not recognize a common law cause of action for loss of parental consortium, and the state statute allows such an action to be brought only by an unmarried dependent.
As noted earlier, Plaintiff's proposed amended complaint includes a count seeking punitive damages against Novartis. (Proposed Amended Compl. ¶¶ 120-24.) However, because all of Plaintiff's underlying causes of action against Novartis are untimely, she may not pursue the company for punitive (or any other) damages.
Plaintiff's proposed amended complaint claims that the applicable statues of limitations on her claims should be equitably tolled by reason of Novartis's fraudulent concealment of "the true risks associated with taking" Zometa. (Proposed Am. Compl. ¶¶ 56-59.) The Second Circuit has stated that equitable tolling is "an extraordinary measure that applies only when plaintiff is prevented from filing despite exercising that level of diligence which could reasonably be expected in the circumstances."
For the reasons stated above, Plaintiff's motion to amend her complaint to add claims against Novartis is denied.