Rose v. Fife

207 Cal. App. 3d 760, 255 Cal. Rptr. 440, 1989 Cal. App. LEXIS 79
CourtCalifornia Court of Appeal
DecidedJanuary 12, 1989
DocketDocket Nos. B031622, B037041
StatusPublished
Cited by27 cases

This text of 207 Cal. App. 3d 760 (Rose v. Fife) is published on Counsel Stack Legal Research, covering California Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Rose v. Fife, 207 Cal. App. 3d 760, 255 Cal. Rptr. 440, 1989 Cal. App. LEXIS 79 (Cal. Ct. App. 1989).

Opinion

Opinion

CROSKEY, J.

In this matter we have, on our motion, consolidated the appeal of plaintiff, Polly Rose, with the petition for writ of mandate filed by defendant G.D. Searle & Co. (Searle). This case arose from injuries which plaintiff alleges she sustained by her use of an intrauterine device (IUD) called the “Copper 7.” Searle manufactures the Copper 7. Defendant Doctor J. Kingsley Fife (Fife) prescribed and inserted the Copper 7 for plaintiff. Both defendants filed motions for summary judgment in which they contended plaintiff’s suit was barred by the statute of limitations. The trial court granted Fife’s motion but denied Searle’s. We conclude that all of plaintiff’s causes of action are barred by the statute of limitations and therefore each defendant is entitled to summary judgment.

Procedural Background

Plaintiff filed her suit against Searle and Fife on February 4, 1986, alleging causes of action against “defendants, and each of them” for products *764 liability, negligence, breach of implied and express warranties and medical malpractice. 1

Searle answered the complaint on March 12, 1986, and asserted as an affirmative defense that plaintiff’s suit was barred by the statute of limitations. Fife filed a demurrer on July 9, 1987, also asserting the statute of limitations. Before the demurrer could be heard, plaintiff filed, on July 30, 1987, a motion for leave to amend her complaint. The trial court granted plaintiff’s motion and the defendants each filed an answer to the first amended complaint. Thereafter, in September 1987 both defendants filed motions for summary judgment, contending plaintiff’s action against them was untimely, Fife citing Code of Civil Procedure section 340.5 and Searle citing section 340, subdivision (3). 2 Plaintiff filed opposition to the motions.

On October 30, 1987, the trial court granted both motions. Later, on its own motion, the court reconsidered defendants’ motions, allowing the parties time to submit supplemental points and authorities and instructing them to consider Kensinger v. Abbott Laboratories (1985) 171 Cal.App.3d 376 [217 Cal.Rptr. 313], Thereafter on November 20, 1987, the trial court granted summary judgment to Fife. It denied Searle’s motion, citing a then pending Supreme Court case, subsequently filed as Jolly v. Eli Lilly & Co. (1988) 44 Cal.3d 1103 [245 Cal.Rptr. 658, 751 P.2d 923], as grounds for so doing. Plaintiff filed an appeal from that portion of the order granting Fife’s motion. 3

Searle filed another motion for summary judgment on July 7, 1988. The trial court denied this motion on August 12 and Searle filed its petition for writ of mandate on September 12. 4 Because they involve *765 essentially identical issues we have ordered Searle’s petition consolidated with plaintiff’s appeal for resolution in a single opinion.

Factual Background

Dr. Fife inserted a Copper 7 into plaintiff in October 1978. He told her to have it replaced in three years and he replaced it in January 1982 with another Copper 7. In her complaint, plaintiff alleged that at the time the Copper 7 was placed in her it was defective and unreasonably dangerous for its intended use because it increased the rate of accidental pregnancies, septic abortions, inflammations, masses, sterility and problems associated with the Fallopian tubes. Plaintiff alleged she “neither knew nor had reason to know at the time of her purchase and acquisition of said Copper 7 or at any time prior to August 18, 1984, of the existence of the foregoing described defect.” Plaintiff alleged that as a proximate result of her use of the Copper 7 she suffered severe permanent internal injuries which have and will necessitate medical attention and loss of wages.

After defendants asserted statute of limitation defenses in their respective answer and demurrer, plaintiff moved for leave to amend her complaint. In a declaration, dated July 27, 1987, and submitted in support of that motion, plaintiff stated that in August 1984 she watched a broadcast of the television show “60 Minutes” in which defects of another intrauterine device (the Daikon Shield) were discussed. She then contacted her attorney, Ronald Cohen, related to him the information from the broadcast and told him she believed she had worn the Daikon Shield. Cohen later contacted her and told her she had worn a Copper 7.

Plaintiff then states in her declaration: “Therefore, at that time, I had no knowledge that the Copper 7 was believed to have caused a number of physical injuries to its users, [fi] However, on or about October 5, 1985, I read an article in the Chicago Tribune which linked the Copper 7 to a number of injuries to women. It was only at this time that I learned that my injuries may have been caused by my use of the Copper 7 device, [fl] Therefore although I was aware that one type of IUD was linked to certain injuries in women in August, 1984, I was not aware that my specific IUD could possibly have caused my problems until October of 1985.” (Italics added.)

Attorney Cohen also submitted a declaration in support of plaintiff’s motion for leave to amend. In it he states that after he got plaintiff’s medical *766 records to determine if she had worn a Daikon Shield, her file lay dormant until she contacted him after reading the newspaper article on the Copper 7. Cohen states: “It was this newspaper article that put Plaintiff on notice that her physical injuries were the result of the Defendant’s IUD.” He also states: “Thus, Paragraph 7 of the complaint herein is mistaken in that [plaintiff] was aware of defects in the Daikon Shield devices [in August of 1984] but not that of Defendant’s Copper 7.”

Cohen contends his own actions support plaintiff’s assertion that it was the newspaper article which caused her to be aware of the Copper 7’s defects. He points to the fact that within one month after the newspaper article was published he sent a section 364 notice to Fife and he filed the instant action as soon as that 90-day notice to Fife had run. He then states: “. . . the complaint therefore should have alleged that Plaintiff first learned of Defendant’s possible negligence on October 5, 1985, as alleged in the First Amended Complaint, not as alleged in Paragraph 7 of the Complaint, or August 18, 1984.” Cohen also requested “that the Complaint be amended so as to more clearly name defendant FIFE as a Defendant in each cause of action.” Plaintiff’s complaint was amended to allege she neither knew nor had reason to know prior to October 5, 1985, of the existence of defects in the Copper 7.

Defendants’ motions for summary judgment were based in part on plaintiff’s deposition taken in May 1987. In her deposition, plaintiff stated that in March 1983 she was hospitalized with a pelvic infection. Both the emergency room doctor and the staff doctor who treated her after she was admitted (Dr. Parks) told her the IUD had to be removed because of the infection.

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Cite This Page — Counsel Stack

Bluebook (online)
207 Cal. App. 3d 760, 255 Cal. Rptr. 440, 1989 Cal. App. LEXIS 79, Counsel Stack Legal Research, https://law.counselstack.com/opinion/rose-v-fife-calctapp-1989.