Bartlett v. Mutual Pharmaceutical

2010 DNH 130
District Court, D. New Hampshire·Decided July 30, 2010·No. CV-08-358-JL·Published·Cited by 3 cases

Opinion

Bartlett v. Mutual Pharmaceutical CV-08-358-JL 7/30/10 UNITED STATES DISTRICT COURT DISTRICT OF NEW HAMPSHIRE

Karen L. Bartlett

v. Civil No. 08-cv-358-JL Opinion No. 2010 DNH 130

Mutual Pharmaceutical Company, Inc.

MEMORANDUM OPINION

Defendant Mutual Pharmaceutical Company has moved for reconsideration of this court's order denying Mutual's summary judgment motion in part and granting it in part. See Bartlett v. M ut. Pharm. C o ., 2010 DNH 112 ("Order").1 Mutual argues that this court made a manifest error of law in ruling that Bartlett could prevail on her strict products liability claim by proving that the product at issue, the prescription drug Sulindac, was "defective because its safety risks outweigh its medical benefits, making it an unreasonably dangerous product," id. at 23 (footnote omitted), without having to prove that the product had some other "defect" in design.

While language in the New Hampshire Supreme Court's opinion in Buckingham v. R.J. Reynolds Tobacco Co., 142 N.H. 822 (1998), arguably supports Mutual's view, its subseguent decision in Vautour v. Body Masters Sports Industries, Inc., 147 N.H. 150

1Document no. 243.

(2001), expressly holds that a plaintiff can prevail on a strict products liability claim by proving that a product was "unreasonably dangerous pursuant to the risk-utility balancing test," without also having to prove "a safer, alternative design," id. at 157. Mutual's motion does not address Vautour's holding and, indeed, barely mentions the case.

Accordingly, as fully explained infra. Mutual's motion to reconsider fails to demonstrate a "manifest error of fact or law," L.R. 7.2(e)," or, so far as the court is concerned, any error at all. The motion is therefore denied.

I. Background The facts relevant to Mutual's motion for summary judgment are set forth throughout the Order and need not be repeated here. Essentially, Bartlett claims that she suffered a painful and life-threatening condition known as Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis, or "SJS/TEN," from taking Sulindac, a generic prescription drug manufactured by Mutual and prescribed by her doctor. In moving for summary judgment. Mutual argued principally that it adeguately warned the doctor of the risk of SJS/TEN but that, even if it had not, any failure to warn was not the cause of Bartlett's injuries because her doctor admitted that he had not read Sulindac's warning label before

prescribing it to her. Mutual argued that those flaws were fatal not only to Bartlett's failure-to-warn claims, but also to her strict products liability claim based on defective design, because "the primary allegation [she] relies upon to support [it] is [her] erroneous contention that Sulindac was defective because it lacked an adeguate warning."

In support of her strict products liability claim, though, "Bartlett also alleges that Sulindac is defective because its safety risks outweigh its medical benefits, making it an unreasonably dangerous product"--as this court ultimately observed in the Order. Thus, following oral argument on Mutual's summary judgment motion, the court ordered both parties to brief whether Bartlett's inability to prove causation on her failure- to-warn claims was also fatal to her strict products liability claim based on defective design.

Mutual maintained that it was, because "the New Hampshire Supreme Court would recognize that in actions involving pharmaceutical products, whether a product is defective in design turns on whether the product was accompanied by an inadeguate warning." According to Mutual, that proposition followed from New Hampshire's embrace of comment k to the Restatement (Second) of Torts § 402A (1965), which. Mutual said, provides that "an unavoidably unsafe product is defective in design only if it is

not accompanied by a proper warning." Because "[w]here a product design cannot be made safer, it is judged by the adeguacy of its warnings," Mutual argued that a causal link between an allegedly inadeguate warning and the plaintiff's injury was essential to a strict liability claim based on an unavoidably unsafe product.

This court accepted Mutual's premise--that New Hampshire would not hold the manufacturer of an important and unavoidably unsafe product strictly liable so long as it was accompanied by an adeguate warning, see Order at 24-25--but rejected Mutual's conclusion that Bartlett's strict liability claim therefore failed for want of proof that the allegedly inadeguate warning caused her injury, id. at 23-24. Instead, the court ruled, if Bartlett could prevail at trial on "whether Sulindac is unreasonably dangerous and whether that defective condition caused her injuries . . . Mutual might nonetheless be able to avoid liability for defective design if it can prove, as an affirmative defense, that Sulindac is unavoidably unsafe and had an adeguate safety warning." Id. at 26. The court refused to enter summary judgment for Mutual based on that defense, however, because "the adeguacy of Sulindac's safety warning is a matter of genuine dispute on this record." Id.

II. Analysis As noted above. Mutual now argues that--quite apart from the adequacy of the warning--Bartlett's strict products liability claim fails because she cannot prove "a defect in the product." Proving that Sulindac's safety risks outweigh its medical benefits, making it unreasonably dangerous, is not enough. Mutual maintains.2 Instead, Mutual says, Bartlett must also prove that Sulindac was "defective"--a concept that Mutual does not attempt to define, but which it insists cannot be proven here, because Sulindac "contains a single active ingredient" and therefore "cannot be made safer, as one would expect of a product containing a design defect."

There are a number of problems with this argument, but the first (and most glaring) is that the New Hampshire Supreme Court expressly rejected it in Vautour. There, the plaintiffs appealed from a directed verdict entered against them on their strict

2In a footnote. Mutual suggests that Bartlett cannot prove even that, because her expert witnesses "do not compare the utility of Mutual's Sulindac to any other medications with respect to their ability to relieve pain and inflammation or to treat patients with . . . any other condition" and "have not even addressed those benefits with respect to Sulindac itself." Because Mutual is not urging reconsideration on this point (and in fact did not even make this argument in support of its summary judgment motion), the court need not consider it here--but will do so at the appropriate point in the proceedings.

products liability claim, arguing that "the superior court erred by reguiring them to prove an alternative design as an additional element in the case." 147 N.H. at 153. The defendant, however, urged the court "to adopt the Restatement (Third) of Torts § 2(b) (1998), which reguires a plaintiff in a design defect case to prove that the risks of harm posed by the product could have been reduced or avoided by a reasonable alternative design." Id. at 154. The court declined, reasoning that "while proof an alternative design is relevant in a design defect case, it should be neither a controlling factor nor an essential element that should be proved in every case." Id. at 156. Instead, the court concluded, "the risk-utility test as currently applied protects the interests of both consumers and manufacturers in design defect cases." Id.

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