78R7315 AJA-F
By: Wohlgemuth H.B. No. 2851
A BILL TO BE ENTITLED
AN ACT
relating to products liability.
BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
SECTION 1. Chapter 82, Civil Practice and Remedies Code, is
amended by adding Sections 82.007-82.009 to read as follows:
Sec. 82.007. PRESCRIPTION DRUGS AND DEVICES. (a) In this
section:
(1) "Device" means a device defined by 21 U.S.C.
Section 321, as amended, and approved by the United States Food and
Drug Administration.
(2) "Drug" means a drug defined by 21 U.S.C. Section
321, as amended, and approved by the United States Food and Drug
Administration.
(3) "Health care" has the meaning assigned by Section
1.03(a), Medical Liability and Insurance Improvement Act of Texas
(Article 4590i, Vernon's Texas Civil Statutes).
(4) "Health care provider" means any person,
partnership, professional association, limited liability company,
corporation, facility, or institution licensed, certified,
registered, or chartered by this state to provide health care,
including a registered nurse, hospital, dentist, podiatrist,
pharmacist, assisted living facility, or nursing home. The term
includes an officer, employee, independent contractor, or agent of
a health care provider or physician acting in the course or scope of
the person's employment.
(b) A health care provider that prescribes a prescription
drug or medical device is not liable to a patient or a third party
for damages arising out of the ingestion of the drug or use of the
device if the drug or device was prescribed in accordance with
instructions approved by the United States Food and Drug
Administration regarding:
(1) dosage and administration of the drug;
(2) indications for which the approved drug should be
taken or for which the device should be used; and
(3) contraindications against taking the drug or using
the device.
(c) A pharmacy or pharmacist that fills a prescription
described by Subsection (b) is not liable for damages arising out of
the ingestion of the drug or use of the device prescribed.
Sec. 82.008. EVIDENCE OF SUBSEQUENT IMPROVEMENTS OR OTHER
MEASURES. In a products liability action, a court may not admit,
except for purposes of impeachment, evidence of a subsequent
improvement made or measure taken with respect to the defect
alleged to have caused harm, or a similar product that, if made or
taken before the product was supplied, would have made the
claimant's harm less likely.
Sec. 82.009. COMPLIANCE WITH GOVERNMENT STANDARDS. (a)
Notwithstanding any other law, a manufacturer or seller of a
product that allegedly caused the claimant's harm is not liable if
the product was manufactured or sold in compliance with a federal or
state law or rule governing the manufacture or sale of the product,
including specifications for manufacturing, using, packaging, or
labeling of the product.
(b) Subsection (a) does not apply to a manufacturer or
seller if a final determination has been made by the regulatory
agency or a court having jurisdiction over the regulatory agency
that the manufacturer or seller intentionally withheld from or
misrepresented to the applicable regulatory agency information
concerning the product and:
(1) the claimant proves by clear and convincing
evidence that the manufacturer knew or should have known that the
withheld or misrepresented information could result in a
potentially harmful product defect; and
(2) the claimant's injuries resulted from the
anticipated defect.
SECTION 2. The changes in law made by this Act apply only to
a cause of action that accrues on or after the effective date of
this Act. A cause of action that accrues before the effective date
of this Act is governed by the law in effect immediately before that
date, and that law is continued in effect for that purpose.
SECTION 3. This Act takes effect September 1, 2003.