Vaught,et al v. Showa Denko K K,etal

CourtCourt of Appeals for the Fifth Circuit
DecidedJune 2, 1997
Docket96-20200
StatusPublished

This text of Vaught,et al v. Showa Denko K K,etal (Vaught,et al v. Showa Denko K K,etal) is published on Counsel Stack Legal Research, covering Court of Appeals for the Fifth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Vaught,et al v. Showa Denko K K,etal, (5th Cir. 1997).

Opinion

REVISED UNITED STATES COURT OF APPEALS FOR THE FIFTH CIRCUIT

_____________________

No. 96-20200 _____________________

JANET L. VAUGHT et al.,

Plaintiffs-Appellants,

versus

SHOWA DENKO K.K. et al.,

Defendants-Appellees.

_________________________________________________________________

Appeals from the United States District Court for the Southern District of Texas

_________________________________________________________________ March 10, 1997

Before HIGGINBOTHAM, SMITH, and BARKSDALE, Circuit Judges.

RHESA HAWKINS BARKSDALE, Circuit Judge:

For this diversity action, the key issues at hand are when the

limitations period began running under Texas law for the Vaughts’ cause of action arising out of Janet L. Vaught’s use of L-

tryptophan, a nutritional supplement, and whether her membership in

a putative federal class action in another State tolled the Texas

limitations period until class certification was denied.

Asserting, inter alia, that a diligent, but fruitless, inquiry was

made as to whether the Vaughts had a cause of action, the Vaughts

challenge the summary judgment granted Defendants on limitations

grounds. We AFFIRM.

I. In August 1987, while hospitalized for injuries received in an

automobile accident, Janet Vaught (Vaught) was prescribed L-

tryptophan, an over-the-counter nutritional supplement. She had

never taken this product. After her hospitalization, however, she

continued to take L-tryptophan for several months pursuant to

prescription purchases. In late 1987 or early 1988, she began to

experience various unexplained physical symptoms: fatigue, swollen

neck glands, sore throats, body aches, burning sensations, tingling

on her legs, and muscle and joint pain. She stopped taking L-

tryptophan in December 1988, when she learned that she was

pregnant.

On 4 April 1990, Vaught read a newspaper article about an

action filed by a Houston, Texas, lawyer on behalf of a woman who

allegedly contracted eosinophilia myalgia syndrome (EMS) from L-

tryptophan. EMS is a multisystemic disorder characterized by severe

muscle and joint pain, swelling of the arms and legs, skin rash,

fever, and sometimes neuropathy, resulting in paralysis and death.

In the fall of 1989, the Food and Drug Administration (FDA)

established that over 280 cases of EMS were connected to the

ingestion of L-tryptophan, a “virtually unequivocal”

epidemiological link. As a result, the FDA issued a nationwide,

mandatory recall of L-tryptophan in late November 1989.

Vaught noticed that she suffered some of the same symptoms

that the newspaper article described as indicative of EMS, such as

fatigue, stiffness, and muscle and joint pain. She contacted a

paralegal (now the Vaughts’ lawyer) in the Houston lawyer’s office,

- 2 - to obtain information about EMS, although Vaught contends that she

did not think she had EMS at that time. Her contact with that law

firm led her to contact two doctors conducting an EMS study at

Baylor University Medical School, Drs. Harati and McKinley.

Dr. McKinley sent her an “L-tryptophan Eosinophilia-Myalgia

Patient Data Sheet”. When Vaught began filling out the

questionnaire on 18 April 1990, she thought she might have EMS, so

she called the Baylor doctors for their opinion. Vaught spoke with

each of them at the end of April.

Also in April 1990, after reading the newspaper article,

Vaught contacted Dr. Keichian, who had treated her for her

automobile accident injuries, and told him that she had taken L-

tryptophan. Dr. Keichian ordered a blood test, and on 25 April

told Vaught that her eosinophil levels were normal and that she did

not have EMS.

That June, Vaught arranged to have an examination done by one

of the Baylor doctors, Dr. Harati. She brought her medical records

and the completed Patient Data Sheet to the examination. Once

again, she was advised that she had normal eosinophil levels in her

blood and did not have EMS. Dr. Harati referred Vaught to Dr.

Croock, a Baylor University rheumatologist, for further evaluation.

Vaught was examined by Dr. Croock on 13 July 1990; he told her

that she was not suffering from EMS but from fibromyalgia or

fibrositis. He gave Vaught information on fibromyalgia and

prescribed Elavil, a tricyclic antidepressant used primarily for

treating that ailment.

- 3 - Vaught took Elavil for approximately six months, and her

condition improved somewhat. Her symptoms, however, never

completely disappeared, in spite of her attempts at other curative

measures, such as physical therapy.

By the end of 1992, Vaught’s condition worsened; she

experienced dizziness, fainting spells, and respiratory and

gastrointestinal problems. In late 1992 or early 1993, she again

became concerned that she might have EMS. She contacted her family

physician, Dr. Fields. And in January 1993, she consulted Dr.

Patton. That February and March, she underwent muscle and sural

nerve biopsies to rule out EMS. Dr. Fields then recommended Vaught

to Dr. Burns; in April 1993, he diagnosed EMS on the basis of

Vaught’s biopsies, medical records, exams, and blood work.

Vaught contacted the paralegal with whom she had spoken in

1990 and who had become a practicing attorney in Houston. On 28

April 1993, Vaught and her husband filed this action in Texas state

court against Showa Denko K.K. and its American distributors; it

was removed to federal court in February 1994. That June, the

Panel on Multidistrict Litigation ordered this action transferred

to the United States District Court for the District of South

Carolina to be joined with pending nationwide L-tryptophan

litigation being conducted there (MDL No. 865). In September 1995,

this action was conditionally remanded to district court in Texas

for further proceedings.

- 4 - Defendants then moved for summary judgment on limitations

grounds. Following a hearing in January 1996, the district court

granted the motion.

II.

The Vaughts present three issues. First, they contend that a

genuine issue of material fact exists as to when their cause of

action accrued. Next, they seek certification of the following

question to the Texas Supreme Court: “Under the Texas discovery

rule, does a plaintiff’s diligent, but fruitless, inquiry into

whether she has an actionable toxic tort suspend the statute of

limitations running against her claim?”. Finally, they maintain

that Janet Vaught’s membership in a putative nationwide L-

tryptophan class action tolled the limitations period until class

certification was denied.

We review a summary judgment de novo, applying the same

standard as the district court. E.g., Bodenheimer v. PPG Indus.,

Inc., 5 F.3d 955, 956 (5th Cir. 1993). Such judgment is

appropriate where “there is no genuine issue as to any material

fact and the movant is entitled to judgment as a matter of law”.

FED. R. CIV. P. 56(c). In making this determination, we are to draw

all reasonable inferences in favor of the nonmovant. E.g.,

Bodenheimer, 5 F.3d at 956. And, because this is a diversity

action, we apply Texas substantive law. Erie R.R. Co. v. Tompkins,

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