Kay v. Johnson & Johnson

722 F. Supp. 874, 1989 U.S. Dist. LEXIS 11740, 1989 WL 117757
CourtDistrict Court, D. Massachusetts
DecidedAugust 30, 1989
DocketCiv. A. 85-3863-WF
StatusPublished
Cited by7 cases

This text of 722 F. Supp. 874 (Kay v. Johnson & Johnson) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Kay v. Johnson & Johnson, 722 F. Supp. 874, 1989 U.S. Dist. LEXIS 11740, 1989 WL 117757 (D. Mass. 1989).

Opinion

MEMORANDUM AND ORDER

WOLF, District Judge.

Plaintiff Martha Kay has brought this products liability action for negligence and breach of warranty against defendants Johnson & Johnson and Ortho Pharmaceutical Corporation (“Ortho”). Plaintiff claims that she suffers from a severe pig-mentary disorder as a result of using Ortho Novum, an oral contraceptive manufactured by Johnson & Johnson and distributed by Ortho. The action was commenced in Massachusetts Superior Court for Bristol County on October 17, 1984. Defendants were served with the summons and complaint on September 30, 1985 and the action was removed to this court on October 11, 1985. Jurisdiction rests on diversity of citizenship. 28 U.S.C. § 1332.

Defendants have moved for summary judgment under Fed.R.Civ.P. 56, claiming that plaintiff’s claims are barred by the applicable three year statutes of limitations because they were not brought until October 17, 1984. 1 See Mass.Gen.Laws c. 260 § 2A (three-year statute of limitations for negligence) and c. 106, § 2-318 (three-year statute of limitations for breach of warranty). Plaintiff opposes the motion for sum *875 mary judgment. The parties have filed memoranda, affidavits, depositions, and other materials. A hearing has been held and the parties have since supplemented their memoranda.

Based on the relevant facts, which the evidence presented does not put in genuine dispute, the court concludes that plaintiff’s claims are barred by the Massachusetts statutes of limitations. Defendants’ motion for summary judgment is, therefore, allowed.

1. FACTS

Unless otherwise indicated, the following facts are not genuinely in dispute. Kay is a registered nurse who received her nursing degree in 1953. From 1953 to 1978, she was employed as a nurse or nurse supervisor at the Truesdale Hospital in Fall River, Massachusetts. Deposition of Martha Kay, Tab D at pp. 7-13. 2 On March 15, 1966, Kay visited her gynecologist, Dr. Alex Friedman, to request that he prescribe an oral contraceptive. Id. at 42-43. Dr. Friedman prescribed Ortho Novum. Friedman Depo., Tab G at 31-32. Kay was taking no other medication at this time. Kay Depo., Tab D at 56.

Within a few months after she began taking Ortho Novum, Kay noticed a darkening of the skin on the right side of her heck. Kay Depo., Tab D at 49. The darkening subsequently spread to her knuckles, ears, legs and arms. Kay Depo., Tab D at 51. Plaintiff was aware of the progression of this condition “as it was occurring.” Plaintiff’s Answer #25 to Defendant Or-tho Pharmaceutical Corporation’s First Set of Interrogatories, Tab C at 23.

Sometime between March 1966 and May 1967, plaintiff brought her condition to the attention of Dr. David Greer, an internist with a subspecialty in endocrinology. Kay Depo., Tab D at 52-55, 58; Greer Depo., Tab I at 4. At that time, Dr. Greer worked with plaintiff at Truesdale Hospital in Fall River. Greer Depo., Tab I at 11-15. Kay testified that in the course of her work as a nurse, she had become aware that oral contraceptives sometimes induce a condition known as “pseudo-pregnancy,” a condition in which non-pregnant women display symptoms of pregnancy, and that chloasma — a darkening of certain areas of the skin — sometimes occurs during pregnancy. Kay Depo., Tab D at 20-24, 32-33. However, she had never before used oral contraceptives herself, and when she first brought her condition to Dr. Greer’s attention, she was concerned that she might have Addison’s disease. Subsequent tests for Addison’s disease were negative. Id. at 52-53.

Dr. Greer testified that Kay told him in an informal hospital encounter that she was concerned about the pigmentation problem, that she had read something in the package insert for Ortho Novum that indicated the Ortho Novum might be associated with the problem, and that she would like his advice as to whether the oral contraceptive might be the cause of this problem. Greer Depo., Tab I at 15-18. Dr. Greer “felt that it was a likely possibility” that her condition was related to her use of Ortho Novum (although he felt there were other possible causes as well), Greer Depo., Tab J at 4, and “told' her it was a possible association, and ... suggested that she discuss it with her doctor who prescribed the medication [Dr. Friedman]_” Greer Depo., Tab I at 17. Dr. Greer never told Kay that the oral contraceptive was the cause of her pigmentation problem. Greer Depo., Tab J at 3.

Kay does not recall Dr. Greer characterizing Ortho Novum as a likely possible cause of her problem, but does acknowledge that he advised her to consult Dr. Friedman. Kay Depo., Tab D at 50-58. Kay then visited Dr. Friedman who, either alone or in consultation with Dr. Greer, diagnosed the problem as chloasma, a pigmentation disorder, and advised plaintiff to discontinue the contraceptive because of this condition. Plaintiff’s Answer # 12 to Ortho Interrogatories, Tab C at 11. Dr. *876 Friedman’s office note concerning Kay, dated May 15, 1967, states “Ortho Novum discontinued because of chloasma.” Friedman Depo., Tab G at 25, 32, 40; Office Records of Dr. Friedman — Truesdale Clinic, Friedman Depo. Ex. 3, Tab H; Kay Depo., Tab D at 54-56; Greer Depo., Tab J at 6.

On the advice of Drs. Greer and Friedman, Kay discontinued using Ortho Novum around May 1967, and remained off the medication for approximately five or six months. Kay Depo., Tab D at 53-54. Rather than receding during this period, however, Kay’s condition worsened, spreading to all areas of her body except her upper arms. Id. at 60. Plaintiff discussed with Dr. Friedman the fact that her pigmentation did not decrease after discontinuing Ortho Novum and told him that she wanted to resume the medication. Id. at 62-63. Dr. Friedman issued her a new prescription. Friedman Depo., Tab G at 32. Because of her fear of other possible side effects, including phlebitis and visual problems, plaintiff again discontinued using Or-tho Novum in May 1968. Kay Depo., Tab D at 19-29, 65-66.

After Kay discontinued Ortho Novum in 1968, her hyperpigmentation continued to spread and become associated with other symptoms, including a burning sensation and a thickening of the skin. Id. at 69-70. Because the condition did not improve, Dr. Greer had discarded the theory that the contraceptive was the cause of her progressive pigmentation. Greer Depo., Tab J at 15-17. During the 1970s and early 1980s, Kay’s condition was evaluated extensively by numerous physicians in a number of medical investigations coordinated by her personal physician, Dr. Greer, in an effort to determine the cause of her condition and an appropriate course of therapy. These evaluations included an examination by professors at Yale Medical School, see Letter dated March 25, 1969 from Dr. Braver-man to Dr. Greer, Greer Depo. Ex. D, Tab L; extensive evaluations of Kay as a research patient at the Yale-New Haven Hospital in several separate admissions, see

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Bluebook (online)
722 F. Supp. 874, 1989 U.S. Dist. LEXIS 11740, 1989 WL 117757, Counsel Stack Legal Research, https://law.counselstack.com/opinion/kay-v-johnson-johnson-mad-1989.